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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

(Mark one)

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended March 31, 2024

OR

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from _________ to _________

Commission File Number: 001-41063

JOURNEY MEDICAL CORPORATION

(Exact name of registrant as specified in its charter)

Delaware

    

47-1879539

(State or other jurisdiction of incorporation or organization)

(I.R.S. Employer Identification No.)

9237 E Via de Ventura Blvd., Suite 105, Scottsdale, AZ 85258

(Address of principal executive offices and zip code)

(480) 434-6670

(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

    

Trading Symbol(s)

    

Name of each exchange on which registered

Common Stock, par value $0.0001 per share

DERM

NASDAQ Capital Market

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes No

Indicate by check mark whether the registrant has submitted electronically, if any, every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes No

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See definition of “large accelerated filer,” “accelerated filer,” “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Large Accelerated Filer

Accelerated Filer

Non-accelerated Filer

Smaller Reporting Company

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

Indicate by check mark whether registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes No

Indicate the number of shares outstanding of each of the registrant’s classes of common stock, as of the latest practicable date.

Class of Common Stock

    

Outstanding Shares as of May 14, 2024

Common Stock Class A, $0.0001 par value

6,000,000

Common Stock, $0.0001 par value

14,012,896

PART I.      FINANCIAL INFORMATION

Item 1.    Condensed Consolidated Financial Statements (unaudited)

JOURNEY MEDICAL CORPORATION

Unaudited Condensed Consolidated Balance Sheets

(Dollars in thousands except for share and per share amounts)

    

March 31,

    

December 31, 

2024

2023

ASSETS

 

  

 

  

Current assets

 

  

 

  

Cash and cash equivalents

 

$

24,057

 

$

27,439

Accounts receivable, net of reserves

 

9,799

 

15,222

Inventory

 

10,580

 

10,206

Prepaid expenses and other current assets

 

2,577

 

3,588

Total current assets

 

47,013

 

56,455

Intangible assets, net

 

19,473

 

20,287

Operating lease right-of-use asset, net

 

79

 

101

Other assets

 

6

 

6

Total assets

$

66,571

$

76,849

LIABILITIES AND STOCKHOLDERS’ EQUITY

 

  

 

  

Current liabilities

 

  

 

  

Accounts payable

$

15,343

$

18,149

Due to related party

 

198

 

195

Accrued expenses

 

20,033

 

20,350

Accrued interest

241

22

Income taxes payable

 

37

 

53

Installment payments – licenses, short-term

 

3,000

 

3,000

Operating lease liability, short-term

 

84

 

99

Total current liabilities

 

38,936

 

41,868

Term loan, long-term, net of debt discount

14,684

14,622

Operating lease liability, long-term

 

 

9

Total liabilities

 

53,620

 

56,499

Commitments and contingencies (Note 13)

 

  

 

  

Stockholders’ equity

 

  

 

  

Common stock, $.0001 par value, 50,000,000 shares authorized, 13,932,310 and 13,323,952 shares issued and outstanding as of March 31, 2024 and December 31, 2023, respectively

 

1

 

1

Common stock - Class A, $.0001 par value, 50,000,000 shares authorized, 6,000,000 shares issued and outstanding as of March 31, 2024 and December 31, 2023

 

1

 

1

Additional paid-in capital

 

95,746

 

92,703

Accumulated deficit

 

(82,797)

 

(72,355)

Total stockholders' equity

 

12,951

 

20,350

Total liabilities and stockholders’ equity

$

66,571

$

76,849

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements

1

JOURNEY MEDICAL CORPORATION

Unaudited Condensed Consolidated Statements of Operations

(Dollars in thousands except for share and per share amounts)

    

Three-Month Periods Ended

March 31, 

    

2024

    

2023

Revenue:

Product revenue, net

$

13,030

$

12,165

Other revenue

48

Total revenue

13,030

12,213

Operating expenses

 

 

Cost of goods sold – product revenue

 

6,816

 

6,449

Research and development

 

7,884

 

2,033

Selling, general and administrative

 

8,420

 

13,292

Total operating expenses

 

23,120

 

21,774

Loss from operations

 

(10,090)

 

(9,561)

Other expense (income)

 

 

Interest income

 

(217)

 

(122)

Interest expense

548

650

Foreign exchange transaction losses

21

47

Total other expense (income)

352

575

Loss before income taxes

 

(10,442)

 

(10,136)

Income tax expense

 

 

Net loss

$

(10,442)

$

(10,136)

Net loss per common share:

Basic and diluted

$

(0.53)

$

(0.57)

Weighted average number of common shares:

 

 

Basic and diluted

 

19,757,449

 

17,807,194

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements

2

JOURNEY MEDICAL CORPORATION

Unaudited Condensed Consolidated Statements of Changes in Stockholders’ Equity

(Dollars in thousands except for share and per share amounts)

Three-Month Period Ended March 31, 2024

Total

    

Common Stock

    

Common Stock A

Additional

Accumulated

Shareholders’

    

Shares

    

Amount

    

Shares

    

Amount

    

Paid-in Capital

    

Deficit

    

Equity

Balance as of December 31, 2023

13,323,952

$

1

 

6,000,000

$

1

$

92,703

$

(72,355)

$

20,350

Share-based compensation

 

 

 

 

1,406

 

 

1,406

Exercise of stock options for cash

55,375

 

 

 

68

 

 

68

Issuance of common stock for vested restricted stock units

211,028

 

 

 

 

-

 

 

-

Issuance of common stock under ESPP

52,211

85

85

Issuance of common stock, ATM offering, net of issuance costs of $46

289,744

1,484

1,484

Net loss

-

(10,442)

(10,442)

Balance as of March 31, 2024

13,932,310

$

1

 

6,000,000

$

1

$

95,746

$

(82,797)

$

12,951

Three-Month Period Ended March 31, 2023

Total

    

Common Stock

Common Stock A

Additional

Accumulated

Shareholders’

    

Shares

    

Amount

    

Shares

    

Amount

    

Paid-in Capital

    

Deficit

    

Equity 

Balance as of December 31, 2022

11,765,700

$

1

 

6,000,000

$

1

$

85,482

$

(68,502)

$

16,982

Share-based compensation

 

 

 

 

646

 

 

646

Issuance of common stock for vested restricted stock units

68,662

 

 

 

 

 

Net loss

 

 

 

 

 

(10,136)

 

(10,136)

Balance as of March 31, 2023

11,834,362

$

1

 

6,000,000

$

1

$

86,128

$

(78,638)

$

7,492

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements

3

JOURNEY MEDICAL CORPORATION

Unaudited Condensed Consolidated Statements of Cash Flows

(Dollars in thousands except for share and per share amounts)

    

Three-Month Periods Ended

March 31, 

    

2024

    

2023

Cash flows from operating activities

  

  

Net loss

$

(10,442)

$

(10,136)

Adjustments to reconcile net loss to net cash used in operating activities:

 

  

 

  

Bad debt expense

 

6

 

126

Non-cash interest expense

 

 

98

Amortization of debt discount

 

62

 

17

Amortization of acquired intangible assets

 

814

 

1,069

Amortization of operating lease right-of-use assets

 

22

 

22

Share-based compensation

 

1,406

 

646

Changes in operating assets and liabilities:

 

 

Accounts receivable

5,417

466

Inventory

 

(374)

 

881

Prepaid expenses and other current assets

 

1,011

 

832

Accounts payable

 

(2,806)

 

7,088

Due to related party

 

3

 

(43)

Accrued expenses

 

(317)

 

(2,013)

Accrued interest

219

5

Income tax payable

 

(16)

 

Lease liabilities

(24)

(14)

Net cash used in operating activities

 

(5,019)

 

(956)

 

 

Cash flows from investing activities

 

 

Acquired intangible assets

 

 

(5,000)

Net cash provided by (used in) investing activities

(5,000)

 

 

Cash flows from financing activities

 

 

Proceeds from exercise of stock options

 

68

 

Proceeds from issuance of common stock, ATM offering, net of issuance costs

 

1,484

 

Issuance of common stock under ESPP

85

Proceeds from line of credit

28,000

Repayments of line of credit

(27,948)

Net cash provided by financing activities

 

1,637

 

52

Net change in cash

 

(3,382)

 

(5,904)

Cash at the beginning of the period

 

27,439

 

32,003

Cash at the end of the period

$

24,057

$

26,099

 

  

 

  

Supplemental disclosure of cash flow information:

Cash paid for interest

$

267

$

535

Cash paid for income taxes

$

$

7

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements

4

JOURNEY MEDICAL CORPORATION

Notes to Unaudited Condensed Consolidated Financial Statements

NOTE 1. ORGANIZATION AND PLAN OF BUSINESS OPERATIONS

Journey Medical Corporation (“Journey” or the “Company”) is a commercial-stage pharmaceutical company that primarily focuses on the selling and marketing of U.S. Food and Drug Administration (“FDA”)-approved prescription pharmaceutical products for the treatment of dermatological conditions. The Company’s current product portfolio includes seven branded and two authorized generic prescription drugs for dermatological conditions that are marketed in the U.S. The Company acquires rights to products and product candidates by licensing or otherwise acquiring an ownership interest in, funding the research and development of, and eventually commercializing, the products through its field sales organization.

As of March 31, 2024 and December 31, 2023, the Company was a majority-owned subsidiary of Fortress Biotech, Inc. (“Fortress” or “Parent”).

Liquidity and Capital Resources

At March 31, 2024, the Company had $24.1 million in cash and cash equivalents as compared to $27.4 million of cash and cash equivalents at December 31, 2023.

On December 27, 2023, the Company entered into a Credit Agreement (the “Credit Agreement”) with SWK Funding LLC (“SWK”). The Credit Agreement provides for a term loan facility (the “Credit Facility”) in the original principal amount of up to $20.0 million. On the closing date, the Company drew $15.0 million. The remaining $5.0 million may be drawn upon the Company’s request within 12 months after the closing date. Loans under the Credit Facility (the “Term Loans”) mature on December 27, 2027, and bear interest at a rate per annum equal to the three-month term Secured Overnight Financing Rate (“SOFR”) (subject to a SOFR floor of 5%) plus 7.75%. The interest rate resets quarterly. Interest payments began in February 2024 and are paid quarterly. Beginning in February 2026, the Company is required to repay a portion of the outstanding principal of the Term Loans quarterly in an amount equal to 7.5% of the principal amount of funded Term Loans.

On December 30, 2022, the Company filed a shelf registration statement on Form S-3 (File No. 333-269079), which was declared effective by the Securities and Exchange Commission (“SEC”) on January 26, 2023. This shelf registration statement covers the offering, issuance and sale by the Company of up to an aggregate of $150.0 million of the Company’s common stock, preferred stock, debt securities, warrants, and units (the “2022 Shelf”). In connection with the 2022 Shelf, the Company entered into an At Market Issuance Sales Agreement (the “Sales Agreement”) relating to shares of the Company’s common stock. The Company may offer and sell up to 4,900,000 shares of its common stock, from time to time, under the Sales Agreement. During the three months ended March 31, 2024, the Company issued and sold 289,744 shares of common stock under the 2022 Shelf, generating net proceeds of $1.5 million. At March 31, 2024, 3,861,553 shares remain available for issuance under the 2022 Shelf.

The Company regularly evaluates market conditions, its liquidity profile, and financing alternatives, including out-licensing arrangements for its products, to enhance its capital structure. The Company may seek to raise capital through debt or equity financings to expand its product portfolio and for other strategic initiatives, which may include sales of securities under either the 2022 Shelf or a new registration statement or drawing on the SWK Credit Facility. The Company cannot make any assurances that such additional financing will be available and, if available, the terms may negatively impact the Company’s business and operations. The Company’s expectations are based on current assumptions, projected commercial sales of products, clinical development plans and regulatory submission timelines, which may be uncertain and may not emerge as expected. Additionally, as a result of recurring losses, substantial doubt exists about the Company’s ability to continue as a going concern for a period of at least twelve months from the date of issuance of these financial statements.

The accompanying financial statements have been prepared on a going concern basis, which contemplates the realization of assets and satisfaction of liabilities in the ordinary course of business. The financial statements do not include any adjustments relating to the recoverability and classification of recorded asset amounts or the amounts and classification of liabilities that may be necessary if the Company is unable to continue as a going concern.

5

NOTE 2. BASIS OF PRESENTATION

Basis of Presentation and Principles of Consolidation

The Company’s consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“GAAP”). The Company’s consolidated financial statements include the accounts of the Company and the accounts of the Company’s wholly-owned subsidiary, JG Pharma, Inc. (“JG” or “JG Pharma”). All intercompany balances and transactions have been eliminated.

Emerging Growth Company

From time to time, new accounting pronouncements are issued by the Financial Accounting Standards Board (“FASB”) or other standard-setting bodies and adopted by the Company as of the specified effective date. Unless otherwise discussed, the impact of recently issued standards that are not yet effective will not have a material impact on the Company’s audited consolidated financial statements upon adoption. Under the Jumpstart Our Business Startups Act of 2012, as amended, the Company meets the definition of an emerging growth company and elected the extended transition period for complying with new or revised accounting standards, which delays the adoption of these accounting standards until they would apply to private companies.

Use of Estimates

The preparation of consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of expenses during the reporting period. Significant estimates made by management include provisions for coupons, chargebacks, wholesaler fees, specialty pharmacy discounts, managed care rebates, product returns, and other allowances customary to the pharmaceutical industry. Significant estimates made by management also include inventory realization, valuation of intangible assets, useful lives of amortizable intangible assets and share-based compensation. Actual results may differ materially and adversely from these estimates. To the extent there are material differences between the estimates and actual results, the Company’s future results of operations will be affected.

Segment Information

Operating segments are defined as components of an enterprise about which separate discrete information is available for evaluation by the chief operating decision maker, or decision-making group, in deciding how to allocate resources and in assessing performance. The Company views its operations and manages its business in one segment, which reflects products for the treatment of dermatological conditions.

NOTE 3. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

The Company’s significant accounting policies are described in Note 2 of the Notes to the Consolidated Financial Statements included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2023 (the “2023 Form 10-K”).

Accounting Standards Note Yet Adopted

In November 2023, the FASB issued Accounting Standards Update (“ASU”) No. 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, which requires that an entity report segment information in accordance with Topic 280, Segment Reporting. The amendment in the ASU is intended to improve reportable segment disclosure requirements primarily through enhanced disclosures about significant segment expenses. The amendments in this update are effective for fiscal years beginning after December 15, 2023, and interim periods within fiscal years beginning after December 15, 2024. The Company is currently evaluating the impact of the new standard on its financial statements and disclosures.

In December 2023, the FASB issued ASU No. 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, which expands disclosures in an entity’s income tax rate reconciliation table and disclosures regarding cash taxes paid both in the U.S. and foreign jurisdictions. The update will be effective for annual periods beginning after December 15, 2024. The Company is currently evaluating the impact that this guidance will have on its financial statements and disclosures.

6

NOTE 4. INVENTORY

The Company’s inventory consists of the following for the periods ended:

    

March 31, 

    

December 31, 

($’s in thousands)

2024

2023

Raw materials

$

4,180

$

4,640

Work-in-process

 

805

 

884

Finished goods

 

5,865

 

4,987

Inventory at cost

10,850

10,511

Inventory reserves

(270)

(305)

Total inventories

$

10,580

$

10,206

NOTE 5. INTANGIBLE ASSETS

The Company’s finite-lived intangible assets consist of acquired intangible assets. The Company’s intangible assets as of March 31, 2024 and December 31, 2023 are summarized as follows:

Estimated

Useful Lives

March 31, 

December 31, 

($’s in thousands)

    

(Years)

    

2024

    

2023

Intangible assets - product licenses

  

3-9

$

37,925

$

37,925

Accumulated amortization

(15,309)

(14,495)

Accumulated impairment loss

 

 

(3,143)

 

(3,143)

Total intangible assets

$

19,473

$

20,287

The Company’s amortization expense for the three-month periods ended March 31, 2024 and 2023 was $0.8 million and $1.1 million, respectively. Amortization expense is recorded as a component of cost of goods sold in the Company’s unaudited condensed consolidated statements of operations.

Future amortization of the Company’s intangible assets is as follows:

For the years ended

    

Total Amortization

Remainder of 2024

$

2,443

December 31, 2025

3,257

December 31, 2026

 

2,471

December 31, 2027

 

1,775

December 31, 2028

 

1,595

Thereafter

 

3,990

Subtotal

15,531

Asset not yet placed in service

 

3,942

Total

$

19,473

NOTE 6. LICENSES ACQUIRED

DFD-29

In June 2021, the Company entered a license, collaboration, and assignment agreement (the “DFD-29 Agreement”) to obtain global rights for the development and commercialization of a late-stage development modified release oral minocycline for the treatment of rosacea (“DFD-29”) with Dr. Reddy’s Laboratories, Ltd (“DRL”); provided, that DRL retained certain rights to the program in select

7

markets including Brazil, Russia, India and China. Pursuant to the terms and conditions of the DFD-29 Agreement, the Company paid $10.0 million. Based on the development and commercialization of DFD-29, additional contingent regulatory and commercial milestone payments totaling up to $155.0 million may also become payable by the Company. The Company is required to pay royalties ranging from approximately ten percent to twenty percent on net sales of the DFD-29 product, subject to certain reductions. Additionally, the Company was required to fund and oversee the Phase 3 clinical trials beginning after the execution of the DFD-29 Agreement in 2021. The Phase 3 clinical trials substantially concluded in July 2023 upon the Company’s receipt of positive Phase 3 clinical trial results.

Qbrexza

In March 2021, the Company executed an Asset Purchase Agreement (the “Qbrexza APA”) with Dermira, Inc., a subsidiary of Eli Lilly and Company (“Dermira”). Pursuant to the terms of the Qbrexza APA, the Company acquired the rights to Qbrexza® (glycopyrronium), a prescription cloth towelette to treat primary axillary hyperhidrosis in patients nine years of age or older. The Company paid the upfront fee of $12.5 million to Dermira. In addition, the Company is obligated to pay Dermira up to $144.0 million in the aggregate upon the achievement of certain sales milestones. The royalty structure for the agreement is tiered with royalties for the first two years ranging from approximately 40% to 30%. Thereafter, royalties are approximately 12.0% to 19.0%. Royalty amounts are subject to certain reductions in the event there is a loss of exclusivity.

Accutane

In July 2020, the Company entered into an exclusive license and supply agreement for Accutane (the “Accutane Agreement”) with DRL. Pursuant to the Accutane Agreement, the Company paid $5.0 million. Three additional milestone payments totaling $17.0 million are contingent upon the achievement of certain net sales milestones. The Company is required to pay royalties in an amount equal to a low-double digit percentage of net sales. The term of the Accutane Agreement is ten years and renewable upon mutual agreement. Each party may terminate the Accutane Agreement for an uncured material breach by the other party or for certain bankruptcy or insolvency related events. The Company may also terminate the Accutane Agreement without cause upon 180 days written notice to DRL.

NOTE 7. FAIR VALUE MEASUREMENTS

Fair value is defined as an exit price, representing the amount that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. As such, fair value is a market-based measurement that should be determined based on assumptions that market participants would use in pricing an asset or a liability.

The accounting guidance requires fair value measurements be classified and disclosed in one of the following three categories:

Level 1: Quoted prices in active markets for identical assets or liabilities.

Level 2: Observable inputs other than Level 1 prices for similar assets or liabilities that are directly or indirectly observable in the marketplace.

Level 3: Unobservable inputs which are supported by little or no market activity and that are financial instruments whose values are determined using pricing models, discounted cash flow methodologies, or similar techniques.

The fair value hierarchy also requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs when measuring fair value.

Certain of the Company’s financial instruments are not measured at fair value on a recurring basis but are recorded at amounts that approximate their fair value due to their liquid or short-term nature, such as accounts payable, accrued expenses and other current liabilities.

8

Financial assets and liabilities measured at fair value on a recurring basis are summarized below:

    

 March 31, 2024

($’s in thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

  

  

  

  

Cash and cash equivalents

$

24,057

$

$

$

24,057

Total

$

24,057

$

$

$

24,057

    

 December 31, 2023

($’s in thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

  

  

  

  

Cash and cash equivalents

$

27,439

$

$

$

27,439

Total

$

27,439

$

$

$

27,439

The Company did not carry any level 2 or level 3 assets or liabilities at March 31, 2024 or December 31, 2023. No transfers occurred between level 1, level 2, and level 3 instruments during the three-month periods ended March 31, 2024 and 2023.

NOTE 8. RELATED PARTY AGREEMENTS

Shared Services Agreement with Fortress

On November 12, 2021, the Company and Fortress entered into an arrangement to share the cost of certain employees (the “Shared Services Agreement”). Fortress’ Executive Chairman and Chief Executive Officer is the Executive Chairman of the Company. Under the terms of the Shared Services Agreement, the Company will reimburse Fortress for the salary and benefit costs associated with these employees based upon actual hours worked on Journey-related projects following the completion of the Company’s initial public offering, which occurred in November 2021. In addition, the Company reimburses Fortress for various payroll-related costs and selling, general and administrative costs incurred by Fortress for the benefit of the Company.

For the three-month periods ended March 31, 2024 and 2023, the Company recorded related party expenses to Fortress of approximately $9,361 and $15,000, respectively. The due to related party liability at March 31, 2024 and December 31, 2023 was $0.2 million and $0.2 million, respectively, and primarily relate to reimbursable expenses incurred by Fortress on behalf of the Company. The Company would have incurred these costs irrespective of the relationship with Fortress.

Fortress Income Tax

At March 31, 2024, 50.43% of all classes of the Company’s outstanding common stock was owned by Fortress. Prior to the Company’s initial public offering of securities in 2021, the Company had been filing consolidated federal tax returns and consolidated or combined state tax returns in multiple jurisdictions with Fortress. The Company may still be required to file combined tax returns in certain “combined filing states.” These jurisdictions generally require corporations engaged in unitary business and meet the capital stock requirement of fifty percent to file a combined state tax return.

Additionally, see Note 16 below for a discussion of income taxes.

9

NOTE 9. ACCRUED EXPENSES

Accrued expenses consisted of the following:

    

March 31, 

    

December 31, 

($’s in thousands)

2024

2023

Accrued expenses:

 

  

 

  

Accrued coupons and rebates

$

7,169

$

9,987

Return reserve

2,806

4,077

Accrued compensation

 

3,599

 

3,374

Accrued royalties payable

1,382

2,015

Accrued legal, accounting and tax

 

335

 

185

Accrued research and development

 

3,034

 

20

Accrued inventory

 

581

 

352

Accrued iPledge program

587

174

Other

 

540

 

166

Total accrued expenses

$

20,033

$

20,350

NOTE 10. OPERATING LEASE OBLIGATIONS

The Company leases 3,681 square feet of office space in Scottsdale, Arizona. In September 2022, the Company amended the lease to extend the lease term for an additional 25 months at an annual rate of approximately $0.1 million. The amended lease will expire on January 31, 2025.

The Company recorded lease expense as follows:

    

Three-Month Periods Ended

March 31,

($’s in thousands)

2024

    

2023

Operating lease cost

$

24

$

24

Variable lease cost

 

1

1

Total lease cost

$

25

$

25

The following table summarizes quantitative information about the Company’s operating leases:

    

Three-Month Periods Ended

March 31,

($’s in thousands)

    

2024

2023

Cash paid for amounts included in the measurement of lease liabilities

$

25

$

17

Weighted-average remaining lease term - operating leases

 

0.8

 

1.8

Weighted-average discount rate - operating leases

 

6.25

%

 

6.25

%

As of March 31, 2024, future minimum lease payments under lease agreements associated with the Company’s operations were as follows:

$’s in thousands

    

    

Remainder of 2024

$

77

2025

 

9

Total lease payments

 

86

Less: present value discount

 

(2)

Total operating lease liabilities

$

84

10

NOTE 11. DEBT

The Company’s debt obligations at March 31, 2024 and December 31, 2023 were as follows:

March 31,

December 31,

($’s in thousands)

    

2024

    

2023

Principal balance

$

15,000

$

15,000

Plus: Exit fee

 

750

 

750

Less: Debt discount and fees

$

(1,066)

$

(1,128)

Net carry amount (Long-term)

$

14,684

$

14,622

SWK Long-Term Debt

On December 27, 2023 (the “Closing Date”), the Company entered into a Credit Agreement with SWK. The Credit Agreement provides for a term loan Credit Facility in the original principal amount of up to $20.0 million. On the Closing Date, the Company drew $15.0 million. The remaining $5.0 million may be drawn upon request by the Company within 12 months after the Closing Date. Term Loans under the Credit Facility mature on December 27, 2027. The Term Loans accrue interest which is payable quarterly in arrears. The Term Loans bear interest at a rate per annum equal to the three-month term SOFR (subject to a SOFR floor of 5%) plus 7.75%. The interest rate resets quarterly.

Beginning in February 2026, the Company is required to repay a portion of the outstanding principal of the Term Loans quarterly in an amount equal to 7.5% of the principal amount of funded Term Loans, with any remaining principal balance due on the maturity date. If the total revenue of the Company, measured on a trailing twelve-month basis, is greater than $70.0 million as of December 31, 2025, the principal repayment start date is extended from February 2026 to February 2027, at which point the Company is required to repay a portion of the outstanding principal of the Term Loans quarterly in an amount equal to 15% of the principal amount of funded Term Loans, with any remaining principal balance due on the maturity date.

The Company may at any time prepay the outstanding principal balance of the Term Loans in whole or in part. Prepayment of the Term Loans is subject to payment of a prepayment premium equal to (i) 2% of the Term Loans prepaid plus the amount of interest that would have been due through the first anniversary of the Closing Date if the Term Loans are prepaid prior to the first anniversary of the Closing Date, (ii) 1% of the Term Loans prepaid if the Term Loans are prepaid on or after the first anniversary of the Closing Date but prior to the second anniversary of the Closing Date, or (iii) 0% if prepaid thereafter.

Upon repayment in full of the Term Loans, the Company will pay an exit fee equal to 5% of the original principal amount of the Term Loans. Additionally, the Company paid an origination fee of $0.2 million on the Closing Date and incurred issuance costs of $0.2 million, both of which have been recorded as a debt discount. The Company is accreting the carrying value of the SWK Term Loan to the original principal balance plus the exit fee over the term of the loan using the effective interest method. The amortization of the discount is accounted for as interest expense. The effective interest rate on the SWK Term Loan as of March 31, 2024 was 15.1%. The fair value of the debt approximates its carrying value.

The SWK Credit Facility also includes both revenue and liquidity covenants, restrictions as to payment of dividends, and is secured by substantially all assets of the Company. As of March 31, 2024, the Company was in compliance with the financial covenants under the SWK Credit Facility.

As of March 31, 2024, the contractual maturities of the long-term debt, including the payment of the exit fee, are as follows (dollars in thousands):

11

Years ending December 31,

    

Term Loan

Remainder of 2024

$

2025

 

2026

 

4,500

2027

 

11,250

Total

 

15,750

Debt discount

 

(1,066)

Total, net

 

14,684

Current portion

 

Term-loan (long-term)

$

14,684

NOTE 12: INTEREST EXPENSE AND FINANCING FEES

Interest expense and financing fees for the three months ended March 31, 2024 consisted of the following:

    

Three-Month Periods Ended March 31,

($’s in thousands)

    

2024

    

2023

Interest payments on term loans and LOC

$

486

$

535

Amortization/Accretion

62

33

Imputed interest on acquired intangible assets

82

Total Interest expense and financing fees

$

548

$

650

NOTE 13. COMMITMENTS AND CONTINGENCIES

License Agreements

The Company has undertaken to make contingent milestone payments to the licensors of its portfolio of drug products and candidates. In addition, the Company is required to pay royalties to such licensors based on a percentage of net sales of each drug candidate following regulatory marketing approval. For additional information on future milestone payments and royalties, see Note 6.

NOTE 14. SHARE-BASED COMPENSATION

In 2015, the Company’s Board of Directors adopted, and stockholders approved, the Journey Medical 2015 Stock Plan (the “Plan”) authorizing the Company to grant shares of common stock to eligible employees, directors, and consultants in the form of restricted stock, restricted stock units (“RSUs”), stock options and other types of grants. The amount, terms, and exercisability provisions of grants are determined by the Board of Directors. The number of shares issuable under the Plan is 7,642,857. As of March 31, 2024, 863,295 shares were available for issuance under the Plan.

The Company, from time to time, grants stock options to employees, non-employees and directors with exercise prices equal to the closing price of the underlying shares of the Company’s common stock on the Nasdaq Capital Market on the date that the options are granted. Options granted have a term of ten years from the grant date. Options granted generally vest over four-year period. Compensation cost for stock options is charged against operations on a straight-line basis over the vesting period. The Company estimates the fair value of stock options on the grant date by applying the Black-Scholes option pricing valuation model.

In 2023, the Company’s Board of Directors adopted, and stockholders approved, the Journey Medical Corporation 2023 Employee Stock Purchase Plan (the “2023 ESPP”). The Company initially reserved 300,000 shares of common stock for future issuance under the 2023 ESPP. As of March 31, 2024, 247,789 shares were available for issuance under the 2023 ESPP.

12

The following table summarizes the components of share-based compensation expense in the consolidated statements of operations for the three-month period ended March 31, 2024 and 2023:

    

Three-Month Periods Ended March 31,

($’s in thousands)

    

2024

    

2023

Research and development

$

145

$

33

Selling, general and administrative

 

1,261

 

613

Total non-cash compensation expense related to share-based compensation included in operating expense

$

1,406

$

646

Stock Options

The following table summarizes the Company’s stock option activities:

Weighted

    

    

Weighted

    

    

average

Number

average

Aggregate

remaining

of

exercise

intrinsic

contractual 

    

Shares

    

price

    

value

    

life (years)

Outstanding options at December 31, 2023

2,769,869

$

1.49

$

6,053,833

4.53

Granted

25,000

4.57

Exercised

(55,375)

1.22

Forfeited

(65,523)

2.91

Expired

(1,250)

2.62

Outstanding options at March 31, 2024

 

2,672,721

$

1.49

$

5,866,003

 

4.23

Options vested and exercisable at March 31, 2024

 

1,991,507

$

0.97

$

5,393,973

 

2.73

For the three-month periods ended March 31, 2024 and 2023, approximately $73,000 and $0.2 million, respectively, of stock option compensation expense was charged against operations. For the three-month period ended March 31, 2024, the Company issued 55,375 shares of common stock upon the exercise of outstanding stock options and received proceeds $67,514. The Company did not issue any shares of common stock upon the exercise of stock options for the three-month period ended March 31, 2023. At March 31, 2024, the Company had unrecognized stock-based compensation expense related to all unvested options of $0.8 million, which the Company expects to recognize over a weighted-average period of approximately 1.8 years.

The aggregate intrinsic value in the previous table reflects the total pre-tax intrinsic value (the difference between the Company’s closing stock price on the last trading day of the period and the exercise price of the options, multiplied by the number of in-the-money stock options) that would have been received by the option holders had all option holders exercised their options on March 31, 2024. The intrinsic value of the Company’s stock options changes based on the closing price of the Company’s common stock.

Restricted Stock Units

The following table summarizes the activity related to the Company’s RSUs for the three-month period ended March 31, 2024:

    

Weighted

Number of

average grant

    

units

    

date Fair value

Unvested balance at December 31, 2023

 

1,306,923

$

3.88

Granted

 

887,500

 

4.97

Vested

(211,028)

3.58

Forfeited

(10,000)

5.02

Unvested balance at March 31, 2024

1,973,395

$

4.40

For the three-month periods ended March 31, 2024 and 2023, approximately $1.3 million and $0.5 million, respectively, of stock compensation expense related to RSUs was charged against operations. For the three-month periods ended March 31, 2024 and 2023

13

the Company issued 211,028 and 68,662 shares of common stock, respectively, upon vesting of RSU’s amounting to $0.8 million and $0.2 million, respectively, in total aggregate fair market value. At March 31, 2024, 1,973,395 RSUs remained unvested and there was approximately $4.6 million of unrecognized compensation cost related to restricted stock which the Company expects to recognize over a weighted-average period of approximately 1.6 years.

Employee Stock Purchase Plan

The 2023 ESPP provides that eligible employees may contribute up to 10% of their eligible earnings toward a semi-annual purchase of the Company’s common stock. The 2023 ESPP is qualified under Section 423 of the Internal Revenue Code. The employee’s purchase price is derived from a formula based on the closing price of the common stock on the first day of the offering period versus the closing price on the last date of purchase (or, if not a trading day, on the immediately preceding trading day). The offering period under the 2023 ESPP has a duration of six months, and the purchase price with respect to each offering period beginning on or after such date is, until otherwise amended, equal to 85% of the lesser of (i) the fair market value of the Company’s common stock at the commencement of the applicable six-month offering period or (ii) the fair market value of the Company’s common stock on the purchase date. The Company estimates the fair value of the common stock under the 2023 ESPP using a Black-Scholes valuation model. The fair value was estimated on the date of grant for the offering period beginning February 1, 2024 using the Black-Scholes option valuation model and the straight-line attribution approach with the following assumptions: risk-free interest rate (5.2%); expected term (0.5 years); expected volatility (98%); and an expected dividend yield (0%). The Company recorded $59,240 of stock-based compensation under the 2023 ESPP for the three-month periods ended March 31, 2024. As of March 31, 2024, there was unrecognized stock-based compensation expense of $106,110 related to the current ESPP offering period, which ends July 31, 2024.

NOTE 15. REVENUES FROM CONTRACTS WITH CUSTOMERS

Disaggregation of Net Revenues

The Company has the following actively marketed products, Qbrexza®, Amzeeq®, Zilxi®, Accutane®, Exelderm®, Targadox®, and Luxamend®. All of the Company’s product revenues are recorded in the U.S.

Revenues by product are summarized as follows:

Three-Month Periods Ended March 31, 

($ in thousands)

    

2024

    

2023

Qbrexza®

$

5,017

$

4,094

Accutane®

 

5,819

 

4,648

Amzeeq®

755

1,193

Zilxi®

273

314

Other / legacy

1,166

1,916

Total product revenues

$

13,030

$

12,165

The Company recognized other revenue as follows:

    

Three-Month Periods Ended March 31,

($in thousands)

2024

2023

Other revenue

 

 

48

Total other revenue

$

$

48

Significant Customers

For the three-month periods ended March 31, 2024 and 2023 there were no customers that accounted for more than 10% of the Company’s total gross product revenue.

At March 31, 2024, one of the Company’s customers accounted for more than 10% of its total accounts receivable balance at 14.0%. At December 31, 2023, one of the Company’s customers accounted for more than 10% of its total accounts receivable balance at 13.0%.

14

NOTE 16. INCOME TAXES

Three-Month Periods Ended

March 31, 

($ in thousands)

    

2024

2023

Net Income (loss) before income taxes

$

(10,442)

$

(10,136)

Provision (benefit) for Income

 

 

Effective tax rate

 

0.0

%

 

0.0

%

The Company records income taxes using the asset and liability method. Deferred income tax assets and liabilities are recognized for the future tax effects attributable to temporary differences between the financial statement carrying amounts of existing assets and liabilities and their respective income tax bases, and operating loss and tax credit carryforwards. The Company establishes a valuation allowance if management believes it is more likely than not that the deferred tax assets will not be recovered based on an evaluation of objective verifiable evidence. Management has considered the Company’s history of book and tax income and losses incurred since inception, and the other positive and negative evidence, and has concluded that it is more likely than not that the Company will not realize the benefits of the net deferred tax assets as of March 31, 2024.

As of March 31, 2024, the Company had no unrecognized tax benefits and does not anticipate any significant change to the unrecognized tax benefit balance.

NOTE 17. NET LOSS PER COMMON SHARE

The Company accounts for and discloses net earnings (loss) per share using the treasury stock method. Net earnings (loss) per share, or basic earnings (loss) per share, is computed by dividing net earnings (loss) by the weighted-average number of shares of common stock outstanding. Net earnings (loss) per share assuming dilutions, or diluted earnings (loss) per share, is computed by reflecting the potential dilution from the exercise of in-the-money stock options and the issuance of non-vested restricted stock units.

The Company’s basic and diluted weighted-average number of common shares outstanding for the three-month periods ended March 31, 2024 and 2023 were as follows:

Three-Month Periods Ended March 31,

    

2024

    

2023

Basic and diluted

19,757,449

17,807,194

Potentially dilutive securities:

Unvested restricted stock units

 

1,973,395

1,931,969

Stock options

 

1,624,382

1,130,557

Total potentially dilutive securities

3,597,777

3,062,526

The Company’s potentially dilutive securities, including unvested restricted stock and options have been excluded from the computation of diluted loss per share for the three-month periods ended March 31, 2024, and 2023, as the effect would be to reduce the loss per share. Therefore, the weighted average common stock outstanding used to calculate both basic and diluted income loss per share is the same for the three-month periods ended March 31, 2024 and 2023.

15

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations Forward-Looking Statements

Certain matters discussed in this report may constitute forward-looking statements for purposes of the Securities Act of 1933, as amended (the “Securities Act”), and the Securities Exchange Act of 1934, as amended (the “Exchange Act”), and involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance or achievements to be materially different from the future results, performance or achievements expressed or implied by such forward-looking statements. The words “anticipate,” “believe,” “estimate,” “may,” “expect,” “will,” “could,” “project,” “should,” “intend” and similar expressions are generally intended to identify forward-looking statements. Our actual results may differ materially from the results anticipated in or implied by these forward-looking statements due to a variety of factors, including, without limitation:

the fact that our products and product candidates are subject to time and cost intensive regulation and clinical testing and as a result, may never be successfully developed or commercialized;
a substantial portion of our sales derive from products that are without patent protection and/or are or may become subject to third-party generic competition, the introduction of new competitor products, or an increase in market share of existing competitor products, any of which could have a significant adverse impact on our operating income;
we operate in a heavily regulated industry, and we cannot predict the impact that any future legislation or administrative or executive action may have on our operations;
our revenue is dependent mainly upon sales of our dermatology products and any setback relating to the sale of such products could impair our operating results;
competition could limit our products’ commercial opportunity and profitability, including competition from manufacturers of generic versions of our products;
the risk that our products do not achieve broad market acceptance, including by government and third-party payors;
our reliance third parties for several aspects of our operations;
our dependence on our ability to identify, develop, and acquire or in-license products and integrate them into our operations, at which we may be unsuccessful;
the dependence of the success of our business, including our ability to finance our company and generate additional revenue, on the successful development and regulatory approval of the DFD-29 product candidate and any future product candidates that we may develop, in-license or acquire;
clinical drug development is very expensive, time consuming, and uncertain and our clinical trials may fail to adequately demonstrate the safety and efficacy of our current or any future product candidates;
our competitors could develop and commercialize products similar or identical to ours;
risks related to the protection of our intellectual property and our potential inability to maintain sufficient patent protection for our technology and products;
our business and operations would suffer in the event of computer system failures, cyber-attacks, or deficiencies in our or our third parties’ cybersecurity;
the effects of major public health issues, epidemics or pandemics on our product revenues and any future clinical trials;
our potential need to raise additional capital;

16

the substantial doubt expressed about our ability to continue as a going concern;
Fortress controls a voting majority of our common stock, which could be detrimental to our other shareholders;
and the risks described in under the section titled “Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2023 (the “2023 Form 10-K”).

The forward-looking statements contained in this report reflect our views and assumptions as of the effective date of this report. New risks and uncertainties arise from time to time, and it is impossible for us to predict these events or how they may affect us. Except as required by law, we assume no responsibility for updating any forward-looking statements.

We qualify all of our forward-looking statements by these cautionary statements. In addition, with respect to all of our forward-looking statements, we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995.

Overview

We are a commercial-stage pharmaceutical company founded in October 2014 that primarily focuses on the selling and marketing of FDA-approved prescription pharmaceutical products for the treatment of dermatological conditions. Our current portfolio includes seven branded and two authorized generic prescription drugs for dermatological conditions that are actively marketed in the U.S. We are managed by experienced life science executives with a track record of creating value for their stakeholders and bringing novel medicines to the market, enabling patients to experience increased quality of life and physicians and other licensed medical professionals to provide better care for their patients. We aim to acquire rights to future products by licensing or otherwise acquiring an ownership interest in, funding the research and development of, and eventually commercializing, the products through our field sales force.

Recent Corporate Highlights

In July 2023, we announced positive topline data from our two DFD-29 Phase 3 clinical trials for the treatment of papulopustular rosacea. The Phase 3 clinical trials achieved the co-primary and all secondary endpoints, the subjects completed the 16-week treatment and the drug was well-tolerated. DFD-29 demonstrated statistical superiority over both the standard of care, Oracea® capsules, and placebo for Investigator’s Global Assessment treatment success and the reduction in the total inflammatory lesion count in both studies. We summitted a New Drug Application (“NDA”) under Section 505(b)(2) of the United States Federal Food, Drug and Cosmetic Act (“FDCA”) with the U.S. Food and Drug Administration (the “FDA”) for DFD-29 on January 4, 2024, paying a $4.0 million filing fee, and expect potential approval from the FDA in the second half of 2024. On March 18, 2024, we announced the FDA accepted the Company’s NDA with a Prescription Drug User Fee Act goal date of November 4, 2024.

Critical Accounting Polices and Uses of Estimates

Our discussion and analysis of our financial condition and results of operations are based on our consolidated financial statements, which we have prepared in accordance with accounting principles generally accepted in the United States. Applying these principles requires our judgment in determining the appropriateness of acceptable accounting principles and methods of application in diverse and complex economic activities. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of revenues, expenses, assets and liabilities, and related disclosure of contingent assets and liabilities. We base our estimates on historical experience and other assumptions that we believe are reasonable under the circumstances. Actual results may differ from these estimates under different assumptions or conditions.

For a discussion of our critical accounting estimates, see the section of the 2023 Form 10-K titled “Management’s Discussion and Analysis of Financial Condition and Results of Operations – Critical Accounting Policies and Use of Estimates.” There were no material changes in our critical accounting estimates or accounting policies from December 31, 2023.

17

Accounting Pronouncements

During the three-month period ended March 31, 2024, there were no new accounting pronouncements or updates to recently issued accounting pronouncements disclosed in the 2023 Form 10-K that are expected to materially affect the Company’s present or future financial statements.

Emerging Growth Company and Smaller Reporting Company Status

We are an emerging growth company, as defined in the Jumpstart Our Business Startups Act of 2012 (“JOBS Act”). Under the JOBS Act, emerging growth companies can delay the adoption of new or revised accounting standards issued subsequent to the enactment of the JOBS Act until such time as those standards apply to private companies. Other exemptions and reduced reporting requirements under the JOBS Act for emerging growth companies include presentation of only two years of audited financial statements in our annual reports on Form 10-K, an exemption from the requirement to provide an auditor’s report on internal controls over financial reporting pursuant to Section 404 of the Sarbanes-Oxley Act of 2002, as amended, an exemption from any requirement that may be adopted by the Public Company Accounting Oversight Board regarding mandatory audit firm rotation and less extensive disclosure about our executive compensation arrangements. We have elected to use the extended transition period for complying with new or revised accounting standards that have different effective dates for public and private companies until the earlier of the date that (i) we are no longer an emerging growth company or (ii) we affirmatively and irrevocably opt out of the extended transition period provided in the JOBS Act.

We are also a “smaller reporting company,” meaning that either (i) the market value of our shares held by non-affiliates is less than $250 million or (ii) the market value of our shares held by non-affiliates is less than $700 million and our annual revenue was less than $100 million during the most recently completed fiscal year. We may continue to be a smaller reporting company if either (i) the market value of our shares held by non-affiliates is less than $250 million or (ii) our annual revenue was less than $100 million during the most recently completed fiscal year and the market value of our shares held by non-affiliates is less than $700 million. As a smaller reporting company, we may choose to present only the two most recent fiscal years of audited financial statements in our Annual Report on Form 10-K, we have reduced disclosure obligations regarding executive compensation, and smaller reporting companies are permitted to delay adoption of certain recent accounting pronouncements discussed in Note 2 to our consolidated financial statements in this report on Form 10-Q.

Results of Operations

The following table summarizes our results of operations for the three-month periods ended March 31, 2024 and 2023:

18

Comparison of the Three-Month Periods Ended March 31, 2024 and 2023

Three-Month Periods Ended March 31, 

Change

($ in thousands, except per share data)

    

2024

    

2023

    

$

    

%

Revenue:

Product revenue, net

 

$

13,030

 

$

12,165

$

865

7

%

Other revenue

48

(48)

-100

%

Total revenue

13,030

12,213

817

7

%

Operating expenses

 

  

 

  

  

  

Cost of goods sold – product revenue

 

6,816

 

6,449

367

6

%

Research and development

 

7,884

 

2,033

5,851

288

%

Selling, general and administrative

 

8,420

 

13,292

(4,872)

-37

%

Total operating expenses

 

23,120

 

21,774

1,346

6

%

Loss from operations

 

(10,090)

 

(9,561)

(529)

6

%

Other expense (income)

 

 

  

  

  

Interest income

 

(217)

 

(122)

(95)

78

%

Interest expense

548

650

(102)

-16

%

Foreign exchange transaction losses

21

47

(26)

-55

%

Total other expense (income)

 

352

 

575

(223)

-39

%

Loss before income taxes

 

(10,442)

 

(10,136)

(306)

3

%

Income tax expense

 

 

0

%

Net loss

$

(10,442)

$

(10,136)

(306)

3

%

Revenues

The following table reflects our net product revenue for the three-month periods ended March 31, 2024 and 2023:

Three-Month Periods Ended

 

March 31

Change

($ in thousands)

    

2024

    

2023

    

$

    

%

Qbrexza®

$

5,017

$

4,094

$

923

23

%

Accutane®

5,819

4,648

1,171

25

%

Amzeeq®

755

1,193

(438)

-37

%

Zilxi®

273

314

(41)

-13

%

Other / legacy

1,166

1,916

(750)

-39

%

Total net product revenue

$

13,030

$

12,165

$

865

7

%

Total net product revenues increased by $0.9 million, or 7%, to $13.0 million for the three-month period ended March 31, 2024, from $12.2 million for the three-month period ended March 31, 2023. The increase is primarily due to an increase in net product revenues for Qbrexza and Accutane as we continue to focus our marketing efforts on these products. The increase was partially offset by a decrease in net products revenues from Amzeeq and Zilxi as a result of lower sales volume and Targadox and Ximino. Targadox continues to experience erosion due to generic competition and we discontinued selling Ximino on September 29, 2023.

Gross-to-Net Sales Accruals

We record gross-to-net sales accruals for other (chargebacks, distributor service fees, prompt pay discounts), sales returns, coupons, managed care rebates, government rebates, and other allowances customary to the pharmaceutical industry.

19

Gross-to-net sales accruals and the balance in the related allowance accounts for the three-month periods ended March 31, 2024 and 2023, were as follows:

Managed

Care

($’s in thousands)

    

Returns

    

Coupons

    

Rebates

    

Other

    

Total

Balance as of December 31, 2023

$

4,077

$

3,444

$

5,210

$

1,386

$

14,117

Current provision related to sales in the current period

128

18,742

4,721

1,981

25,572

Payments/adjustments

(1,399)

(19,429)

(6,486)

(2,429)

(29,743)

Balance as of March 31, 2024

$

2,806

$

2,757

$

3,445

$

938

$

9,946

Managed

Care

($’s in thousands)

    

Returns

    

Coupons

    

Rebates

    

Other

    

Total

Balance as of December 31, 2022

$

3,689

$

1,696

$

3,594

$

2,399

$

11,378

Current provision related to sales in the current period

2,091

27,930

5,572

3,927

39,520

Payments/adjustments

(2,409)

(27,409)

(5,475)

(4,008)

(39,301)

Balance as of March 31, 2023

$

3,371

$

2,217

$

3,691

$

2,318

$

11,597

Gross-to-net sales accruals are primarily a function of product sales volume, mix of products sold, and contractual discounts or rebates. Our reserves for gross-to-net sales allowances were $9.9 million at March 31, 2024, compared to $11.6 million at March 31, 2023, a decrease of $1.7 million. The decrease is largely driven by decreases in our reserves for government rebates. Since July 1, 2023, we no longer participate in the Medicaid Drug Rebate Program.

Cost of Goods Sold

Cost of goods sold increased by $0.4 million, or 6%, to $6.8 million for the three-month period ended March 31, 2024, from $6.4 million for the three-month period ended March 31, 2023, due to the increase in net product revenue.

Research and Development

Research and Development expense increased by $5.9 million, to $7.9 million for the three-month period ended March 31, 2024, from $2.0 million for the three-month period ended March 31, 2023. The increase is driven by the $4.0 million filing fee payment to the FDA in January 2024 for DFD-29 and $3.0 million expense for the contractual milestone payment owed to Dr. Reddy’s Laboratories, Ltd (“DRL”) triggered by the FDA’s acceptance of our DFD-29 product NDA in March 2024. This was partially offset by lower clinical trial expenses to develop our DFD-29 product as the project concludes.

Selling, General and Administrative

Selling, general and administrative (“SG&A”) expenses decreased by $4.9 million, or 37%, to $8.4 million for the three-month period ended March 31, 2024, from $13.3 million for the three-month period ended March 31, 2023. The decrease is mainly due to our continued expense management efforts, primarily in sales and marketing and other SG&A areas, designed to improve operational efficiencies, optimize expenses and reduce overall costs.

Interest Expense

Interest expense decreased by $0.1 million to $0.5 million for the three-month period ended March 31, 2024, from $0.6 million for the three-month period ended March 31, 2023. The decrease is primarily attributable to a lower principal balance outstanding during the three-months ended March 31, 2024 of $15.0 million as compared to $20.0 million during the three-months ended March 31, 2023.

Liquidity and Capital Resources

At March 31, 2024, we had $24.1 million in cash and cash equivalents as compared to $27.4 million of cash and cash equivalents at December 31, 2023.

20

On December 27, 2023, we entered into a Credit Agreement (the “Credit Agreement”) with SWK Funding LLC (“SWK”). The Credit Agreement provides for a term loan facility (the “Credit Facility”) in the original principal amount of up to $20.0 million. On the closing date, we drew $15.0 million. The remaining $5.0 million may be drawn at our request within 12 months after the closing date. Loans under the Credit Facility (the “Term Loans”) mature on December 27, 2027, and bear interest at a rate per annum equal to the three-month term Secured Overnight Financing Rate (“SOFR”) (subject to a SOFR floor of 5%) plus 7.75%. The interest rate resets quarterly. Interest payments began in February 2024 and are paid quarterly. Beginning in February 2026, we are required to repay a portion of the outstanding principal of the Term Loans quarterly in an amount equal to 7.5% of the principal amount of funded Term Loans. The SWK Credit Facility also includes both revenue and liquidity covenants, restrictions as to payment of dividends, and is secured by substantially all assets of the Company. As of March 31, 2023, and as of the date of this Quarterly Report on Form 10-Q, the Company was in compliance with the financial covenants under the SWK Credit Facility.

On December 30, 2022, we filed a shelf registration statement on Form S-3 (File No. 333-269079), which was declared effective by the Securities and Exchange Commission (“SEC”) on January 26, 2023. This shelf registration statement covers the offering, issuance and sale of up to an aggregate of $150.0 million of our common stock, preferred stock, debt securities, warrants, and units (the “2022 Shelf”). In connection with the 2022 Shelf, we entered into an At Market Issuance Sales Agreement (the “Sales Agreement”) relating to shares of our common stock. We may offer and sell up to 4,900,000 shares of its common stock, from time to time, under the Sales Agreement. During the three months ended March 31, 2024, we issued and sold 289,744 shares of common stock under the 2022 Shelf, generating net proceeds of $1.5 million. At March 31, 2024, 3,861,553 shares remain available for issuance under the 2022 Shelf.

We regularly evaluate market conditions, our liquidity profile, and financing alternatives, including out-licensing arrangements for our products to enhance our capital structure. We may seek to raise capital through debt or equity financings to expand our product portfolio and for other strategic initiatives, which may include sales of securities under either the 2022 Shelf or a new registration statement or drawing on the SWK Credit Facility. We cannot make any assurances that such additional financing will be available and, if available, the terms may negatively impact the Company’s business and operations. Our expectations are based on current assumptions, projected commercial sales of our products, clinical development plans and regulatory submission timelines, which may be uncertain and may not emerge as expected. Additionally, as a result of recurring losses, substantial doubt exists about our ability to continue as a going concern for a period of at least twelve months from the date of issuance of these financial statements.

Cash Flows for the Three-Month Periods Ended March 31, 2024 and 2023

Three-Month Periods Ended March 31, 

Increase

($’s in thousands)

    

2024

    

2023

    

(Decrease)

Net cash used in operating activities

$

(5,019)

$

(956)

$

(4,063)

Net cash provided by (used in) investing activities

 

 

(5,000)

 

5,000

Net cash provided by financing activities

 

1,637

 

52

 

1,585

Net change in cash and cash equivalents

(3,382)

(5,904)

2,522

Operating Activities

Net cash flows used in operating activities for the three-month period ended March 31, 2024 increased by $4.1 million to $5.0 million from net cash flows used by operating activities of $1.0 million for the three-month period ended March 31, 2023. The increase was driven primarily by changes in net working capital primarily attributable to accounts receivable collections offset by vendor payables from our continued expense management efforts resulting in comparably lower vendor payables from the first quarter of 2023, and inventory, in addition to the net loss for the first quarter 2024.

Investing Activities

Net cash used in investing activities decreased by $5.0 million from period to period. The three-month period ended March 31, 2023 reflects the $5.0 million deferred cash payment paid in January 2023 related to the Vyne Product Acquisition.

21

Financing Activities

Net cash flows provided by financing activities for three-month period ended March 31, 2024 increased by $1.6 million to $1.6 million from $0.1 million of cash flows provided by financing activities for the three-month period ended March 31, 2023. The increase is driven primarily by the net proceeds from issuances of common stock under our ATM.

Material Cash Requirements

In the normal course of business, we enter into contractual obligations that contain cash requirements of which the most significant currently include the following:

We are required to make regular payments under the SWK Credit Facility. Based on the amount currently outstanding under the SWK facility and current interest rates, and assuming we do not make further draws under the SWK facility, we expect to make the following payments:

    

Payments by Period

    

Total

    

Remainder of 2024

    

2025

    

2026

    

2027

($'s in thousands)

Interest

$

6,273

$

1,501

$

1,993

$

1,693

$

1,086

Principal

 

15,000

 

 

 

4,500

 

10,500

Exit fee

 

750

 

 

 

 

750

Total

$

22,023

$

1,501

$

1,993

$

6,193

$

12,336

Should we elect to borrow the remaining $5.0 undrawn balance under the SWB facility, we would expect to repay additional amounts each year until maturity.

Pursuant to the Vyne Product Acquisition Agreement, upon the achievement of net sales milestones with respect to the products purchased in the Vyne Product Acquisition, we are also required to pay contingent consideration consisting of a one-time payment, per product, of $10.0 million and $20.0 million upon each product reaching annual net sales of $100 million and $200 million, respectively. Each required payment must only be paid one time following the first achievement of the applicable annual net sales milestone amount.
On June 29, 2021, we entered into the DFD-29 Agreement to obtain the global rights for the development and commercialization of DFD-29 with DRL. Based on the development and commercialization of DFD-29, additional contingent regulatory and commercial milestone payments totaling up to $155.0 million may also become payable. Royalties ranging from ten percent to twenty percent are payable on net sales of the product. In January 2024, the Company paid a $4.0 million filing fee to the FDA upon filing of an NDA for DFD-29. The Company made a $3.0 million contractual milestone payment to DRL in April 2024 based on the FDA’s acceptance of our NDA for DFD-29 filed in January 2024.
We are contractually obligated to make installment milestone payments of $3.0 million on Ximino, all of which is classified as current.
We are contractually obligated to make sales-based royalty payments to Dermira (for Qbrexza), Sun Pharmaceutical Industries (for Exelderm) and PuraCap Caribe (for Targadox). Due to the contingent nature of these obligations, the amounts of these payments cannot be reasonably predicted.

Item 3. Quantitative and Qualitative Disclosures about Market Risk

We are a smaller reporting company as defined by Rule 12b-2 of the Exchange Act and are not required to provide the information otherwise required under this item.

22

Item 4. Controls and Procedures

Evaluation of Disclosure Controls and Procedures

Under the supervision and with the participation of our management, including our principal executive officer and principal financial officer, we conducted an evaluation of the effectiveness, as of March 31, 2024, of the design and operation of our disclosure controls and procedures, as such term is defined in Exchange Act Rules 13a-15(e) and 15d-15(e). Based on this evaluation, our principal executive officer and principal financial officer have concluded that, as of such date, our disclosure controls and procedures are effective to ensure that information required to be disclosed by us in our Exchange Act reports is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms, and that such information is accumulated and communicated to our management, including our principal executive officer and principal financial officer, as appropriate to allow timely decisions regarding required disclosure.

Changes in Internal Control over Financial Reporting

No change in internal control over financial reporting occurred during the most recent quarter with respect to our operations; which materially affected, or is reasonable likely to materially affect, our internal controls over financial reporting.

23

Part II. Other Information

Item 1. Legal Proceedings.

To our knowledge, there are no legal proceedings pending against us, other than routine actions, administrative proceedings, and other actions not deemed material, that are expected to have a material adverse effect on our financial condition, results of operations, or cash flows. In the ordinary course of business, however, the Company may be subject to both insured and uninsured litigation. Suits and claims may be brought against the Company by customers, suppliers, partners and/or third parties (including tort claims for personal injury arising from clinical trials of the Company’s product candidates and property damage) alleging deficiencies in performance, breach of contract, etc., and seeking resulting alleged damages.

Item 1A. Risk Factors.

We have disclosed under the heading “Risk Factors” in the 2023 Form 10-K a number of risks which may materially affect our business, financial condition or results of operations. You should carefully consider these Risk Factors and other information set forth elsewhere in this Quarterly Report on Form 10-Q. You should be aware that these risk factors and other information may not describe every risk facing our Company. Additional risks and uncertainties not currently known to us may also materially adversely affect our business, financial condition and/or results of operations.

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds.

During the period covered by this report, we have not sold any equity securities in transactions that were not registered under the Securities Act, and neither we nor our affiliates have purchased any equity securities issued by us.

Item 3. Defaults Upon Senior Securities.

None.

Item 4. Mine Safety Disclosures.

Not Applicable.

Item 5. Other Information.

None.

24

Item 6. Exhibits

Exhibit No.

    

Description

3.1

Third Amended and Restated Certificate of Incorporation of Journey Medical Corporation, filed as Exhibit 3.1 to Form 10-K, filed on March 28, 2022 and incorporated herein by reference.

3.2

Amended and Restated Bylaws of Journey Medical Corporation, filed as Exhibit 3.2 to Form 10-K, filed on March 28, 2022 and incorporated herein by reference.

4.1

Form of Common Stock Certificate, filed as Exhibit 4.1 to Form S-1, filed on October 22, 2021 and incorporated herein by reference.

31.1

Certification of Chief Executive Officer of Journey Medical Corporation pursuant to Rule 13a-14(a)/15d-14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002, dated May 14, 2024.**

31.2

Certification of Principal Financial Officer of Journey Medical Corporation pursuant to Rule 13a-14(a)/15d-14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002, dated May 14, 2024.**

32.1

Certification of Chief Executive Officer of Journey Medical Corporation pursuant to 18 U.S.C. §1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, dated May 14, 2024.***

32.2

Certification of Principal Financial Officer of Journey Medical Corporation pursuant to 18 U.S.C. §1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, dated May 14, 2024.***

101

The following financial information from the Company’s quarterly report on Form 10-Q for the period ended March 31, 2024, formatted in Inline Extensible Business Reporting Language (XBRL): (i) the Condensed Consolidated Balance Sheets, (ii) the Condensed Consolidated Statements of Operations, (iii) the Condensed Consolidated Statement of Stockholders’ Equity, (iv) the Condensed Consolidated Statements of Cash Flows, and (v) Notes to the Condensed Consolidated Financial Statements (filed herewith).**

104

Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101).**

**   Filed herewith.

*** Furnished herewith.

25

SIGNATURES

Pursuant to the requirements of the Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

Journey Medical Corporation

(Registrant)

Date: May 14, 2024

By:

/s/ Claude Maraoui

Claude Maraoui

President and Chief Executive Officer

(Principal Executive Officer)

Date: May 14, 2024

By:

/s/ Joseph Benesch

Joseph Benesch

Chief Financial Officer

(Principal Financial Officer)

26

Exhibit 31.1

CERTIFICATION OF PRINCIPAL EXECUTIVE OFFICER

PURSUANT TO RULES 13A-14(A) AND 15D-14(A) UNDER THE SECURITIES EXCHANGE ACT OF 1934,

AS ADOPTED PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002

I, Claude Maraoui, certify that:

1.

I have reviewed this report on Form 10-Q of Journey Medical Corporation;

2.

Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

3.

Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

4.

The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

(a)

Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;

(b)

Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;

(c)

Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

(d)

Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and

5.

The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of registrant’s board of directors (or persons performing the equivalent functions):

(a)

All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and

(b)

Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

    

/s/ Claude Maraoui

Claude Maraoui

President and Chief Executive Officer

(Principal Executive Officer)

May 14, 2024


Exhibit 31.2

CERTIFICATION OF PRINCIPAL FINANCIAL OFFICER

PURSUANT TO RULES 13A-14(A) AND 15D-14(A) UNDER THE SECURITIES EXCHANGE ACT OF 1934,

AS ADOPTED PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002

I, Joseph Benesch certify that:

1.

I have reviewed this report on Form 10-Q of Journey Medical Corporation;

2.

Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

3.

Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

4.

The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15I and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

(a)

Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;

(b)

Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principle;

(c)

Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

(d)

Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and

5.

The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of registrant’s board of directors (or persons performing the equivalent functions):

(a)

All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and

(b)

Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

    

/s/ Joseph Benesch

Joseph Benesch

Chief Financial Officer

(Principal Financial Officer)

May 14, 2024


Exhibit 32.1

CERTIFICATION OF PRINCIPAL EXECUTIVE OFFICER

PURSUANT TO 18 U.S.C. SECTION 1350,

AS ADOPTED PURSUANT TO

SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002

I, Claude Maraoui, President and Chief Executive Officer of Journey Medical Corporation (the “Company”), in compliance with 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, hereby certify that, to the best of my knowledge, the Company’s quarterly report on Form 10-Q for the period ended March 31, 2024 (the “Report”) filed with the Securities and Exchange Commission:

Fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

    

/s/ Claude Maraoui

Claude Maraoui

President and Chief Executive Officer

(Principal Executive Officer)

May 14, 2024


Exhibit 32.2

CERTIFICATION OF PRINCIPAL FINANCIAL OFFICER

PURSUANT TO 18 U.S.C. SECTION 1350,

AS ADOPTED PURSUANT TO

SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002

I, Joseph Benesch, Chief Financial Officer of Journey Medical Corporation (the “Company”), in compliance with 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, hereby certify that, to the best of my knowledge, the Company’s quarterly report on Form 10-Q for the period ended March 31, 2024 (the “Report”) filed with the Securities and Exchange Commission:

Fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and
The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

    

/s/ Joseph Benesch

Joseph Benesch

Chief Financial Officer

(Principal Financial Officer)

May 14, 2024


v3.24.1.1.u2
Document and Entity Information
3 Months Ended
Mar. 31, 2024
shares
Document Type 10-Q
Document Quarterly Report true
Document Period End Date Mar. 31, 2024
Document Transition Report false
Entity File Number 001-41063
Entity Registrant Name JOURNEY MEDICAL CORPORATION
Entity Incorporation, State or Country Code DE
Entity Tax Identification Number 47-1879539
Entity Address, Address Line One 9237 E Via de Ventura Blvd.
Entity Address, Address Line Two Suite 105
Entity Address, City or Town Scottsdale
Entity Address, State or Province AZ
Entity Address, Postal Zip Code 85258
City Area Code 480
Local Phone Number 434-6670
Title of 12(b) Security Common Stock, par value $0.0001 per share
Trading Symbol DERM
Security Exchange Name NASDAQ
Entity Current Reporting Status Yes
Entity Interactive Data Current Yes
Entity Filer Category Non-accelerated Filer
Entity Small Business true
Entity Emerging Growth Company true
Entity Ex Transition Period false
Entity Shell Company false
Entity Central Index Key 0001867066
Current Fiscal Year End Date --12-31
Document Fiscal Year Focus 2024
Document Fiscal Period Focus Q1
Amendment Flag false
Common Stock Class A  
Entity Common Stock, Shares Outstanding 6,000,000
Common stock  
Entity Common Stock, Shares Outstanding 14,012,896
v3.24.1.1.u2
Unaudited Condensed Consolidated Balance Sheets - USD ($)
$ in Thousands
Mar. 31, 2024
Dec. 31, 2023
Current assets    
Cash and cash equivalents $ 24,057 $ 27,439
Accounts receivable, net of reserves 9,799 15,222
Inventory 10,580 10,206
Prepaid expenses and other current assets 2,577 3,588
Total current assets 47,013 56,455
Intangible assets, net 19,473 20,287
Operating lease right-of-use asset, net 79 101
Other assets 6 6
Total assets 66,571 76,849
Current liabilities    
Accounts payable 15,343 18,149
Due to related party $ 198 $ 195
Other Liability, Current, Related Party, Type [Extensible Enumeration] us-gaap:RelatedPartyMember us-gaap:RelatedPartyMember
Accrued expenses $ 20,033 $ 20,350
Accrued interest 241 22
Income taxes payable 37 53
Installment payments - licenses, short-term 3,000 3,000
Operating lease liability, short-term 84 99
Total current liabilities 38,936 41,868
Term loan, long-term, net of debt discount 14,684 14,622
Operating lease liability, long-term   9
Total liabilities 53,620 56,499
Commitments and contingencies (Note 13)
Stockholders' equity    
Additional paid-in capital 95,746 92,703
Accumulated deficit (82,797) (72,355)
Total stockholders' equity 12,951 20,350
Total liabilities and stockholders' equity 66,571 76,849
Common stock    
Stockholders' equity    
Common stock 1 1
Common Stock Class A    
Stockholders' equity    
Common stock $ 1 $ 1
v3.24.1.1.u2
Unaudited Condensed Consolidated Balance Sheets (Parenthetical) - $ / shares
Mar. 31, 2024
Dec. 31, 2023
Common stock    
Par value $ 0.0001 $ 0.0001
Common stock authorized 50,000,000 50,000,000
Common stock issued 13,932,310 13,323,952
Common stock outstanding 13,932,310 13,323,952
Common Class A    
Par value $ 0.0001 $ 0.0001
Common stock authorized 50,000,000 50,000,000
Common stock issued 6,000,000 6,000,000
Common stock outstanding 6,000,000 6,000,000
v3.24.1.1.u2
Unaudited Condensed Consolidated Statements of Operations - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Revenue:    
Product revenue, net $ 13,030 $ 12,165
Other revenue   48
Total revenue 13,030 12,213
Operating expenses    
Cost of goods sold - product revenue 6,816 6,449
Research and development 7,884 2,033
Selling, general and administrative 8,420 13,292
Total operating expenses 23,120 21,774
Loss from operations (10,090) (9,561)
Other expense (income)    
Interest income (217) (122)
Interest expense 548 650
Foreign exchange transaction losses 21 47
Total other expense (income) 352 575
Loss before income taxes (10,442) (10,136)
Net loss $ (10,442) $ (10,136)
Net loss per common share:    
Basic $ (0.53) $ (0.57)
Diluted $ (0.53) $ (0.57)
Weighted average number of common shares:    
Basic 19,757,449 17,807,194
Diluted 19,757,449 17,807,194
v3.24.1.1.u2
Unaudited Condensed Consolidated Statements of Changes in Stockholders' Equity - USD ($)
$ in Thousands
Common Stock
Common Class A
Common Stock
Additional Paid-in Capital
Accumulated Deficit
Total
Balance at beginning at Dec. 31, 2022 $ 1 $ 1 $ 85,482 $ (68,502) $ 16,982
Balance at beginning (in shares) at Dec. 31, 2022 6,000,000 11,765,700      
CONSOLIDATED STATEMENT OF CHANGES IN STOCKHOLDERS' EQUITY          
Share-based compensation     646   646
Issuance of common stock for vested restricted stock units (in shares)   68,662      
Net loss       (10,136) (10,136)
Balance at ending at Mar. 31, 2023 $ 1 $ 1 86,128 (78,638) 7,492
Balance at ending (in shares) at Mar. 31, 2023 6,000,000 11,834,362      
Balance at beginning at Dec. 31, 2023 $ 1 $ 1 92,703 (72,355) 20,350
Balance at beginning (in shares) at Dec. 31, 2023 6,000,000 13,323,952      
CONSOLIDATED STATEMENT OF CHANGES IN STOCKHOLDERS' EQUITY          
Share-based compensation     1,406   1,406
Exercise of stock options for cash     68   68
Exercise of stock options for cash (In shares)   55,375      
Issuance of common stock under ESPP     85   85
Issuance of common stock under ESPP (in shares)   52,211,000      
Issuance of common stock, ATM offering, net of issuance costs of $46     1,484   1,484
Issuance of common stock, ATM offering, net of issuance costs of $46 (in shares)   289,744      
Issuance of common stock for vested restricted stock units (in shares)   211,028      
Net loss       (10,442) (10,442)
Balance at ending at Mar. 31, 2024 $ 1 $ 1 $ 95,746 $ (82,797) $ 12,951
Balance at ending (in shares) at Mar. 31, 2024 6,000,000 13,932,310      
v3.24.1.1.u2
Unaudited Condensed Consolidated Statements of Changes in Stockholders' Equity (Parenthetical)
$ in Thousands
3 Months Ended
Mar. 31, 2024
USD ($)
Unaudited Condensed Consolidated Statements of Changes in Stockholders' Equity  
Stock issuance costs $ 46
v3.24.1.1.u2
Unaudited Condensed Consolidated Statements of Cash Flows - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Cash flows from operating activities    
Net loss $ (10,442) $ (10,136)
Adjustments to reconcile net loss to net cash used in operating activities:    
Bad debt expense 6 126
Non-cash interest expense   98
Amortization of debt discount 62 17
Amortization of acquired intangible assets 814 1,069
Amortization of operating lease right-of-use assets 22 22
Share-based compensation 1,406 646
Changes in operating assets and liabilities:    
Accounts receivable 5,417 466
Inventory (374) 881
Prepaid expenses and other current assets 1,011 832
Accounts payable (2,806) 7,088
Due to related party 3 (43)
Accrued expenses (317) (2,013)
Accrued interest 219 5
Income tax payable (16)  
Lease liabilities (24) (14)
Net cash used in operating activities (5,019) (956)
Cash flows from investing activities    
Acquired intangible assets   (5,000)
Net cash provided by (used in) investing activities   (5,000)
Cash flows from financing activities    
Proceeds from exercise of stock options 68  
Proceeds from issuance of common stock, ATM offering, net of issuance costs 1,484  
Issuance of common stock under ESPP 85  
Proceeds from line of credit   28,000
Repayments of line of credit   (27,948)
Net cash provided by financing activities 1,637 52
Net change in cash (3,382) (5,904)
Cash at the beginning of the period 27,439 32,003
Cash at the end of the period 24,057 26,099
Supplemental disclosure of cash flow information:    
Cash paid for interest $ 267 535
Cash paid for income taxes   $ 7
v3.24.1.1.u2
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS
3 Months Ended
Mar. 31, 2024
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS  
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS

NOTE 1. ORGANIZATION AND PLAN OF BUSINESS OPERATIONS

Journey Medical Corporation (“Journey” or the “Company”) is a commercial-stage pharmaceutical company that primarily focuses on the selling and marketing of U.S. Food and Drug Administration (“FDA”)-approved prescription pharmaceutical products for the treatment of dermatological conditions. The Company’s current product portfolio includes seven branded and two authorized generic prescription drugs for dermatological conditions that are marketed in the U.S. The Company acquires rights to products and product candidates by licensing or otherwise acquiring an ownership interest in, funding the research and development of, and eventually commercializing, the products through its field sales organization.

As of March 31, 2024 and December 31, 2023, the Company was a majority-owned subsidiary of Fortress Biotech, Inc. (“Fortress” or “Parent”).

Liquidity and Capital Resources

At March 31, 2024, the Company had $24.1 million in cash and cash equivalents as compared to $27.4 million of cash and cash equivalents at December 31, 2023.

On December 27, 2023, the Company entered into a Credit Agreement (the “Credit Agreement”) with SWK Funding LLC (“SWK”). The Credit Agreement provides for a term loan facility (the “Credit Facility”) in the original principal amount of up to $20.0 million. On the closing date, the Company drew $15.0 million. The remaining $5.0 million may be drawn upon the Company’s request within 12 months after the closing date. Loans under the Credit Facility (the “Term Loans”) mature on December 27, 2027, and bear interest at a rate per annum equal to the three-month term Secured Overnight Financing Rate (“SOFR”) (subject to a SOFR floor of 5%) plus 7.75%. The interest rate resets quarterly. Interest payments began in February 2024 and are paid quarterly. Beginning in February 2026, the Company is required to repay a portion of the outstanding principal of the Term Loans quarterly in an amount equal to 7.5% of the principal amount of funded Term Loans.

On December 30, 2022, the Company filed a shelf registration statement on Form S-3 (File No. 333-269079), which was declared effective by the Securities and Exchange Commission (“SEC”) on January 26, 2023. This shelf registration statement covers the offering, issuance and sale by the Company of up to an aggregate of $150.0 million of the Company’s common stock, preferred stock, debt securities, warrants, and units (the “2022 Shelf”). In connection with the 2022 Shelf, the Company entered into an At Market Issuance Sales Agreement (the “Sales Agreement”) relating to shares of the Company’s common stock. The Company may offer and sell up to 4,900,000 shares of its common stock, from time to time, under the Sales Agreement. During the three months ended March 31, 2024, the Company issued and sold 289,744 shares of common stock under the 2022 Shelf, generating net proceeds of $1.5 million. At March 31, 2024, 3,861,553 shares remain available for issuance under the 2022 Shelf.

The Company regularly evaluates market conditions, its liquidity profile, and financing alternatives, including out-licensing arrangements for its products, to enhance its capital structure. The Company may seek to raise capital through debt or equity financings to expand its product portfolio and for other strategic initiatives, which may include sales of securities under either the 2022 Shelf or a new registration statement or drawing on the SWK Credit Facility. The Company cannot make any assurances that such additional financing will be available and, if available, the terms may negatively impact the Company’s business and operations. The Company’s expectations are based on current assumptions, projected commercial sales of products, clinical development plans and regulatory submission timelines, which may be uncertain and may not emerge as expected. Additionally, as a result of recurring losses, substantial doubt exists about the Company’s ability to continue as a going concern for a period of at least twelve months from the date of issuance of these financial statements.

The accompanying financial statements have been prepared on a going concern basis, which contemplates the realization of assets and satisfaction of liabilities in the ordinary course of business. The financial statements do not include any adjustments relating to the recoverability and classification of recorded asset amounts or the amounts and classification of liabilities that may be necessary if the Company is unable to continue as a going concern.

v3.24.1.1.u2
BASIS OF PRESENTATION
3 Months Ended
Mar. 31, 2024
BASIS OF PRESENTATION  
BASIS OF PRESENTATION

NOTE 2. BASIS OF PRESENTATION

Basis of Presentation and Principles of Consolidation

The Company’s consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“GAAP”). The Company’s consolidated financial statements include the accounts of the Company and the accounts of the Company’s wholly-owned subsidiary, JG Pharma, Inc. (“JG” or “JG Pharma”). All intercompany balances and transactions have been eliminated.

Emerging Growth Company

From time to time, new accounting pronouncements are issued by the Financial Accounting Standards Board (“FASB”) or other standard-setting bodies and adopted by the Company as of the specified effective date. Unless otherwise discussed, the impact of recently issued standards that are not yet effective will not have a material impact on the Company’s audited consolidated financial statements upon adoption. Under the Jumpstart Our Business Startups Act of 2012, as amended, the Company meets the definition of an emerging growth company and elected the extended transition period for complying with new or revised accounting standards, which delays the adoption of these accounting standards until they would apply to private companies.

Use of Estimates

The preparation of consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of expenses during the reporting period. Significant estimates made by management include provisions for coupons, chargebacks, wholesaler fees, specialty pharmacy discounts, managed care rebates, product returns, and other allowances customary to the pharmaceutical industry. Significant estimates made by management also include inventory realization, valuation of intangible assets, useful lives of amortizable intangible assets and share-based compensation. Actual results may differ materially and adversely from these estimates. To the extent there are material differences between the estimates and actual results, the Company’s future results of operations will be affected.

Segment Information

Operating segments are defined as components of an enterprise about which separate discrete information is available for evaluation by the chief operating decision maker, or decision-making group, in deciding how to allocate resources and in assessing performance. The Company views its operations and manages its business in one segment, which reflects products for the treatment of dermatological conditions.

v3.24.1.1.u2
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
3 Months Ended
Mar. 31, 2024
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES  
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

NOTE 3. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

The Company’s significant accounting policies are described in Note 2 of the Notes to the Consolidated Financial Statements included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2023 (the “2023 Form 10-K”).

Accounting Standards Note Yet Adopted

In November 2023, the FASB issued Accounting Standards Update (“ASU”) No. 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, which requires that an entity report segment information in accordance with Topic 280, Segment Reporting. The amendment in the ASU is intended to improve reportable segment disclosure requirements primarily through enhanced disclosures about significant segment expenses. The amendments in this update are effective for fiscal years beginning after December 15, 2023, and interim periods within fiscal years beginning after December 15, 2024. The Company is currently evaluating the impact of the new standard on its financial statements and disclosures.

In December 2023, the FASB issued ASU No. 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, which expands disclosures in an entity’s income tax rate reconciliation table and disclosures regarding cash taxes paid both in the U.S. and foreign jurisdictions. The update will be effective for annual periods beginning after December 15, 2024. The Company is currently evaluating the impact that this guidance will have on its financial statements and disclosures.

v3.24.1.1.u2
INVENTORY
3 Months Ended
Mar. 31, 2024
INVENTORY  
INVENTORY

NOTE 4. INVENTORY

The Company’s inventory consists of the following for the periods ended:

    

March 31, 

    

December 31, 

($’s in thousands)

2024

2023

Raw materials

$

4,180

$

4,640

Work-in-process

 

805

 

884

Finished goods

 

5,865

 

4,987

Inventory at cost

10,850

10,511

Inventory reserves

(270)

(305)

Total inventories

$

10,580

$

10,206

v3.24.1.1.u2
INTANGIBLE ASSETS
3 Months Ended
Mar. 31, 2024
INTANGIBLE ASSETS  
INTANGIBLE ASSETS

NOTE 5. INTANGIBLE ASSETS

The Company’s finite-lived intangible assets consist of acquired intangible assets. The Company’s intangible assets as of March 31, 2024 and December 31, 2023 are summarized as follows:

Estimated

Useful Lives

March 31, 

December 31, 

($’s in thousands)

    

(Years)

    

2024

    

2023

Intangible assets - product licenses

  

3-9

$

37,925

$

37,925

Accumulated amortization

(15,309)

(14,495)

Accumulated impairment loss

 

 

(3,143)

 

(3,143)

Total intangible assets

$

19,473

$

20,287

The Company’s amortization expense for the three-month periods ended March 31, 2024 and 2023 was $0.8 million and $1.1 million, respectively. Amortization expense is recorded as a component of cost of goods sold in the Company’s unaudited condensed consolidated statements of operations.

Future amortization of the Company’s intangible assets is as follows:

For the years ended

    

Total Amortization

Remainder of 2024

$

2,443

December 31, 2025

3,257

December 31, 2026

 

2,471

December 31, 2027

 

1,775

December 31, 2028

 

1,595

Thereafter

 

3,990

Subtotal

15,531

Asset not yet placed in service

 

3,942

Total

$

19,473

v3.24.1.1.u2
LICENSES ACQUIRED
3 Months Ended
Mar. 31, 2024
LICENSES ACQUIRED  
LICENSES ACQUIRED

NOTE 6. LICENSES ACQUIRED

DFD-29

In June 2021, the Company entered a license, collaboration, and assignment agreement (the “DFD-29 Agreement”) to obtain global rights for the development and commercialization of a late-stage development modified release oral minocycline for the treatment of rosacea (“DFD-29”) with Dr. Reddy’s Laboratories, Ltd (“DRL”); provided, that DRL retained certain rights to the program in select

markets including Brazil, Russia, India and China. Pursuant to the terms and conditions of the DFD-29 Agreement, the Company paid $10.0 million. Based on the development and commercialization of DFD-29, additional contingent regulatory and commercial milestone payments totaling up to $155.0 million may also become payable by the Company. The Company is required to pay royalties ranging from approximately ten percent to twenty percent on net sales of the DFD-29 product, subject to certain reductions. Additionally, the Company was required to fund and oversee the Phase 3 clinical trials beginning after the execution of the DFD-29 Agreement in 2021. The Phase 3 clinical trials substantially concluded in July 2023 upon the Company’s receipt of positive Phase 3 clinical trial results.

Qbrexza

In March 2021, the Company executed an Asset Purchase Agreement (the “Qbrexza APA”) with Dermira, Inc., a subsidiary of Eli Lilly and Company (“Dermira”). Pursuant to the terms of the Qbrexza APA, the Company acquired the rights to Qbrexza® (glycopyrronium), a prescription cloth towelette to treat primary axillary hyperhidrosis in patients nine years of age or older. The Company paid the upfront fee of $12.5 million to Dermira. In addition, the Company is obligated to pay Dermira up to $144.0 million in the aggregate upon the achievement of certain sales milestones. The royalty structure for the agreement is tiered with royalties for the first two years ranging from approximately 40% to 30%. Thereafter, royalties are approximately 12.0% to 19.0%. Royalty amounts are subject to certain reductions in the event there is a loss of exclusivity.

Accutane

In July 2020, the Company entered into an exclusive license and supply agreement for Accutane (the “Accutane Agreement”) with DRL. Pursuant to the Accutane Agreement, the Company paid $5.0 million. Three additional milestone payments totaling $17.0 million are contingent upon the achievement of certain net sales milestones. The Company is required to pay royalties in an amount equal to a low-double digit percentage of net sales. The term of the Accutane Agreement is ten years and renewable upon mutual agreement. Each party may terminate the Accutane Agreement for an uncured material breach by the other party or for certain bankruptcy or insolvency related events. The Company may also terminate the Accutane Agreement without cause upon 180 days written notice to DRL.

v3.24.1.1.u2
FAIR VALUE MEASUREMENTS
3 Months Ended
Mar. 31, 2024
FAIR VALUE MEASUREMENTS  
FAIR VALUE MEASUREMENTS

NOTE 7. FAIR VALUE MEASUREMENTS

Fair value is defined as an exit price, representing the amount that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. As such, fair value is a market-based measurement that should be determined based on assumptions that market participants would use in pricing an asset or a liability.

The accounting guidance requires fair value measurements be classified and disclosed in one of the following three categories:

Level 1: Quoted prices in active markets for identical assets or liabilities.

Level 2: Observable inputs other than Level 1 prices for similar assets or liabilities that are directly or indirectly observable in the marketplace.

Level 3: Unobservable inputs which are supported by little or no market activity and that are financial instruments whose values are determined using pricing models, discounted cash flow methodologies, or similar techniques.

The fair value hierarchy also requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs when measuring fair value.

Certain of the Company’s financial instruments are not measured at fair value on a recurring basis but are recorded at amounts that approximate their fair value due to their liquid or short-term nature, such as accounts payable, accrued expenses and other current liabilities.

Financial assets and liabilities measured at fair value on a recurring basis are summarized below:

    

 March 31, 2024

($’s in thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

  

  

  

  

Cash and cash equivalents

$

24,057

$

$

$

24,057

Total

$

24,057

$

$

$

24,057

    

 December 31, 2023

($’s in thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

  

  

  

  

Cash and cash equivalents

$

27,439

$

$

$

27,439

Total

$

27,439

$

$

$

27,439

The Company did not carry any level 2 or level 3 assets or liabilities at March 31, 2024 or December 31, 2023. No transfers occurred between level 1, level 2, and level 3 instruments during the three-month periods ended March 31, 2024 and 2023.

v3.24.1.1.u2
RELATED PARTY AGREEMENTS
3 Months Ended
Mar. 31, 2024
RELATED PARTY AGREEMENTS  
RELATED PARTY AGREEMENTS

NOTE 8. RELATED PARTY AGREEMENTS

Shared Services Agreement with Fortress

On November 12, 2021, the Company and Fortress entered into an arrangement to share the cost of certain employees (the “Shared Services Agreement”). Fortress’ Executive Chairman and Chief Executive Officer is the Executive Chairman of the Company. Under the terms of the Shared Services Agreement, the Company will reimburse Fortress for the salary and benefit costs associated with these employees based upon actual hours worked on Journey-related projects following the completion of the Company’s initial public offering, which occurred in November 2021. In addition, the Company reimburses Fortress for various payroll-related costs and selling, general and administrative costs incurred by Fortress for the benefit of the Company.

For the three-month periods ended March 31, 2024 and 2023, the Company recorded related party expenses to Fortress of approximately $9,361 and $15,000, respectively. The due to related party liability at March 31, 2024 and December 31, 2023 was $0.2 million and $0.2 million, respectively, and primarily relate to reimbursable expenses incurred by Fortress on behalf of the Company. The Company would have incurred these costs irrespective of the relationship with Fortress.

Fortress Income Tax

At March 31, 2024, 50.43% of all classes of the Company’s outstanding common stock was owned by Fortress. Prior to the Company’s initial public offering of securities in 2021, the Company had been filing consolidated federal tax returns and consolidated or combined state tax returns in multiple jurisdictions with Fortress. The Company may still be required to file combined tax returns in certain “combined filing states.” These jurisdictions generally require corporations engaged in unitary business and meet the capital stock requirement of fifty percent to file a combined state tax return.

Additionally, see Note 16 below for a discussion of income taxes.

v3.24.1.1.u2
ACCRUED EXPENSES
3 Months Ended
Mar. 31, 2024
ACCRUED EXPENSES  
ACCRUED EXPENSES

NOTE 9. ACCRUED EXPENSES

Accrued expenses consisted of the following:

    

March 31, 

    

December 31, 

($’s in thousands)

2024

2023

Accrued expenses:

 

  

 

  

Accrued coupons and rebates

$

7,169

$

9,987

Return reserve

2,806

4,077

Accrued compensation

 

3,599

 

3,374

Accrued royalties payable

1,382

2,015

Accrued legal, accounting and tax

 

335

 

185

Accrued research and development

 

3,034

 

20

Accrued inventory

 

581

 

352

Accrued iPledge program

587

174

Other

 

540

 

166

Total accrued expenses

$

20,033

$

20,350

v3.24.1.1.u2
OPERATING LEASE OBLIGATIONS
3 Months Ended
Mar. 31, 2024
OPERATING LEASE OBLIGATIONS  
OPERATING LEASE OBLIGATIONS

NOTE 10. OPERATING LEASE OBLIGATIONS

The Company leases 3,681 square feet of office space in Scottsdale, Arizona. In September 2022, the Company amended the lease to extend the lease term for an additional 25 months at an annual rate of approximately $0.1 million. The amended lease will expire on January 31, 2025.

The Company recorded lease expense as follows:

    

Three-Month Periods Ended

March 31,

($’s in thousands)

2024

    

2023

Operating lease cost

$

24

$

24

Variable lease cost

 

1

1

Total lease cost

$

25

$

25

The following table summarizes quantitative information about the Company’s operating leases:

    

Three-Month Periods Ended

March 31,

($’s in thousands)

    

2024

2023

Cash paid for amounts included in the measurement of lease liabilities

$

25

$

17

Weighted-average remaining lease term - operating leases

 

0.8

 

1.8

Weighted-average discount rate - operating leases

 

6.25

%

 

6.25

%

As of March 31, 2024, future minimum lease payments under lease agreements associated with the Company’s operations were as follows:

$’s in thousands

    

    

Remainder of 2024

$

77

2025

 

9

Total lease payments

 

86

Less: present value discount

 

(2)

Total operating lease liabilities

$

84

v3.24.1.1.u2
DEBT
3 Months Ended
Mar. 31, 2024
DEBT  
DEBT

NOTE 11. DEBT

The Company’s debt obligations at March 31, 2024 and December 31, 2023 were as follows:

March 31,

December 31,

($’s in thousands)

    

2024

    

2023

Principal balance

$

15,000

$

15,000

Plus: Exit fee

 

750

 

750

Less: Debt discount and fees

$

(1,066)

$

(1,128)

Net carry amount (Long-term)

$

14,684

$

14,622

SWK Long-Term Debt

On December 27, 2023 (the “Closing Date”), the Company entered into a Credit Agreement with SWK. The Credit Agreement provides for a term loan Credit Facility in the original principal amount of up to $20.0 million. On the Closing Date, the Company drew $15.0 million. The remaining $5.0 million may be drawn upon request by the Company within 12 months after the Closing Date. Term Loans under the Credit Facility mature on December 27, 2027. The Term Loans accrue interest which is payable quarterly in arrears. The Term Loans bear interest at a rate per annum equal to the three-month term SOFR (subject to a SOFR floor of 5%) plus 7.75%. The interest rate resets quarterly.

Beginning in February 2026, the Company is required to repay a portion of the outstanding principal of the Term Loans quarterly in an amount equal to 7.5% of the principal amount of funded Term Loans, with any remaining principal balance due on the maturity date. If the total revenue of the Company, measured on a trailing twelve-month basis, is greater than $70.0 million as of December 31, 2025, the principal repayment start date is extended from February 2026 to February 2027, at which point the Company is required to repay a portion of the outstanding principal of the Term Loans quarterly in an amount equal to 15% of the principal amount of funded Term Loans, with any remaining principal balance due on the maturity date.

The Company may at any time prepay the outstanding principal balance of the Term Loans in whole or in part. Prepayment of the Term Loans is subject to payment of a prepayment premium equal to (i) 2% of the Term Loans prepaid plus the amount of interest that would have been due through the first anniversary of the Closing Date if the Term Loans are prepaid prior to the first anniversary of the Closing Date, (ii) 1% of the Term Loans prepaid if the Term Loans are prepaid on or after the first anniversary of the Closing Date but prior to the second anniversary of the Closing Date, or (iii) 0% if prepaid thereafter.

Upon repayment in full of the Term Loans, the Company will pay an exit fee equal to 5% of the original principal amount of the Term Loans. Additionally, the Company paid an origination fee of $0.2 million on the Closing Date and incurred issuance costs of $0.2 million, both of which have been recorded as a debt discount. The Company is accreting the carrying value of the SWK Term Loan to the original principal balance plus the exit fee over the term of the loan using the effective interest method. The amortization of the discount is accounted for as interest expense. The effective interest rate on the SWK Term Loan as of March 31, 2024 was 15.1%. The fair value of the debt approximates its carrying value.

The SWK Credit Facility also includes both revenue and liquidity covenants, restrictions as to payment of dividends, and is secured by substantially all assets of the Company. As of March 31, 2024, the Company was in compliance with the financial covenants under the SWK Credit Facility.

As of March 31, 2024, the contractual maturities of the long-term debt, including the payment of the exit fee, are as follows (dollars in thousands):

Years ending December 31,

    

Term Loan

Remainder of 2024

$

2025

 

2026

 

4,500

2027

 

11,250

Total

 

15,750

Debt discount

 

(1,066)

Total, net

 

14,684

Current portion

 

Term-loan (long-term)

$

14,684

v3.24.1.1.u2
INTEREST EXPENSE AND FINANCING FEES
3 Months Ended
Mar. 31, 2024
INTEREST EXPENSE AND FINANCING FEES  
INTEREST EXPENSE AND FINANCING FEES

NOTE 12: INTEREST EXPENSE AND FINANCING FEES

Interest expense and financing fees for the three months ended March 31, 2024 consisted of the following:

    

Three-Month Periods Ended March 31,

($’s in thousands)

    

2024

    

2023

Interest payments on term loans and LOC

$

486

$

535

Amortization/Accretion

62

33

Imputed interest on acquired intangible assets

82

Total Interest expense and financing fees

$

548

$

650

v3.24.1.1.u2
COMMITMENTS AND CONTINGENCIES
3 Months Ended
Mar. 31, 2024
COMMITMENTS AND CONTINGENCIES  
COMMITMENTS AND CONTINGENCIES

NOTE 13. COMMITMENTS AND CONTINGENCIES

License Agreements

The Company has undertaken to make contingent milestone payments to the licensors of its portfolio of drug products and candidates. In addition, the Company is required to pay royalties to such licensors based on a percentage of net sales of each drug candidate following regulatory marketing approval. For additional information on future milestone payments and royalties, see Note 6.

v3.24.1.1.u2
SHARE-BASED COMPENSATION
3 Months Ended
Mar. 31, 2024
SHARE-BASED COMPENSATION  
SHARE-BASED COMPENSATION

NOTE 14. SHARE-BASED COMPENSATION

In 2015, the Company’s Board of Directors adopted, and stockholders approved, the Journey Medical 2015 Stock Plan (the “Plan”) authorizing the Company to grant shares of common stock to eligible employees, directors, and consultants in the form of restricted stock, restricted stock units (“RSUs”), stock options and other types of grants. The amount, terms, and exercisability provisions of grants are determined by the Board of Directors. The number of shares issuable under the Plan is 7,642,857. As of March 31, 2024, 863,295 shares were available for issuance under the Plan.

The Company, from time to time, grants stock options to employees, non-employees and directors with exercise prices equal to the closing price of the underlying shares of the Company’s common stock on the Nasdaq Capital Market on the date that the options are granted. Options granted have a term of ten years from the grant date. Options granted generally vest over four-year period. Compensation cost for stock options is charged against operations on a straight-line basis over the vesting period. The Company estimates the fair value of stock options on the grant date by applying the Black-Scholes option pricing valuation model.

In 2023, the Company’s Board of Directors adopted, and stockholders approved, the Journey Medical Corporation 2023 Employee Stock Purchase Plan (the “2023 ESPP”). The Company initially reserved 300,000 shares of common stock for future issuance under the 2023 ESPP. As of March 31, 2024, 247,789 shares were available for issuance under the 2023 ESPP.

The following table summarizes the components of share-based compensation expense in the consolidated statements of operations for the three-month period ended March 31, 2024 and 2023:

    

Three-Month Periods Ended March 31,

($’s in thousands)

    

2024

    

2023

Research and development

$

145

$

33

Selling, general and administrative

 

1,261

 

613

Total non-cash compensation expense related to share-based compensation included in operating expense

$

1,406

$

646

Stock Options

The following table summarizes the Company’s stock option activities:

Weighted

    

    

Weighted

    

    

average

Number

average

Aggregate

remaining

of

exercise

intrinsic

contractual 

    

Shares

    

price

    

value

    

life (years)

Outstanding options at December 31, 2023

2,769,869

$

1.49

$

6,053,833

4.53

Granted

25,000

4.57

Exercised

(55,375)

1.22

Forfeited

(65,523)

2.91

Expired

(1,250)

2.62

Outstanding options at March 31, 2024

 

2,672,721

$

1.49

$

5,866,003

 

4.23

Options vested and exercisable at March 31, 2024

 

1,991,507

$

0.97

$

5,393,973

 

2.73

For the three-month periods ended March 31, 2024 and 2023, approximately $73,000 and $0.2 million, respectively, of stock option compensation expense was charged against operations. For the three-month period ended March 31, 2024, the Company issued 55,375 shares of common stock upon the exercise of outstanding stock options and received proceeds $67,514. The Company did not issue any shares of common stock upon the exercise of stock options for the three-month period ended March 31, 2023. At March 31, 2024, the Company had unrecognized stock-based compensation expense related to all unvested options of $0.8 million, which the Company expects to recognize over a weighted-average period of approximately 1.8 years.

The aggregate intrinsic value in the previous table reflects the total pre-tax intrinsic value (the difference between the Company’s closing stock price on the last trading day of the period and the exercise price of the options, multiplied by the number of in-the-money stock options) that would have been received by the option holders had all option holders exercised their options on March 31, 2024. The intrinsic value of the Company’s stock options changes based on the closing price of the Company’s common stock.

Restricted Stock Units

The following table summarizes the activity related to the Company’s RSUs for the three-month period ended March 31, 2024:

    

Weighted

Number of

average grant

    

units

    

date Fair value

Unvested balance at December 31, 2023

 

1,306,923

$

3.88

Granted

 

887,500

 

4.97

Vested

(211,028)

3.58

Forfeited

(10,000)

5.02

Unvested balance at March 31, 2024

1,973,395

$

4.40

For the three-month periods ended March 31, 2024 and 2023, approximately $1.3 million and $0.5 million, respectively, of stock compensation expense related to RSUs was charged against operations. For the three-month periods ended March 31, 2024 and 2023

the Company issued 211,028 and 68,662 shares of common stock, respectively, upon vesting of RSU’s amounting to $0.8 million and $0.2 million, respectively, in total aggregate fair market value. At March 31, 2024, 1,973,395 RSUs remained unvested and there was approximately $4.6 million of unrecognized compensation cost related to restricted stock which the Company expects to recognize over a weighted-average period of approximately 1.6 years.

Employee Stock Purchase Plan

The 2023 ESPP provides that eligible employees may contribute up to 10% of their eligible earnings toward a semi-annual purchase of the Company’s common stock. The 2023 ESPP is qualified under Section 423 of the Internal Revenue Code. The employee’s purchase price is derived from a formula based on the closing price of the common stock on the first day of the offering period versus the closing price on the last date of purchase (or, if not a trading day, on the immediately preceding trading day). The offering period under the 2023 ESPP has a duration of six months, and the purchase price with respect to each offering period beginning on or after such date is, until otherwise amended, equal to 85% of the lesser of (i) the fair market value of the Company’s common stock at the commencement of the applicable six-month offering period or (ii) the fair market value of the Company’s common stock on the purchase date. The Company estimates the fair value of the common stock under the 2023 ESPP using a Black-Scholes valuation model. The fair value was estimated on the date of grant for the offering period beginning February 1, 2024 using the Black-Scholes option valuation model and the straight-line attribution approach with the following assumptions: risk-free interest rate (5.2%); expected term (0.5 years); expected volatility (98%); and an expected dividend yield (0%). The Company recorded $59,240 of stock-based compensation under the 2023 ESPP for the three-month periods ended March 31, 2024. As of March 31, 2024, there was unrecognized stock-based compensation expense of $106,110 related to the current ESPP offering period, which ends July 31, 2024.

v3.24.1.1.u2
REVENUES FROM CONTRACTS WITH CUSTOMERS
3 Months Ended
Mar. 31, 2024
REVENUES FROM CONTRACTS WITH CUSTOMERS  
REVENUES FROM CONTRACTS WITH CUSTOMERS

NOTE 15. REVENUES FROM CONTRACTS WITH CUSTOMERS

Disaggregation of Net Revenues

The Company has the following actively marketed products, Qbrexza®, Amzeeq®, Zilxi®, Accutane®, Exelderm®, Targadox®, and Luxamend®. All of the Company’s product revenues are recorded in the U.S.

Revenues by product are summarized as follows:

Three-Month Periods Ended March 31, 

($ in thousands)

    

2024

    

2023

Qbrexza®

$

5,017

$

4,094

Accutane®

 

5,819

 

4,648

Amzeeq®

755

1,193

Zilxi®

273

314

Other / legacy

1,166

1,916

Total product revenues

$

13,030

$

12,165

The Company recognized other revenue as follows:

    

Three-Month Periods Ended March 31,

($in thousands)

2024

2023

Other revenue

 

 

48

Total other revenue

$

$

48

Significant Customers

For the three-month periods ended March 31, 2024 and 2023 there were no customers that accounted for more than 10% of the Company’s total gross product revenue.

At March 31, 2024, one of the Company’s customers accounted for more than 10% of its total accounts receivable balance at 14.0%. At December 31, 2023, one of the Company’s customers accounted for more than 10% of its total accounts receivable balance at 13.0%.

v3.24.1.1.u2
INCOME TAXES
3 Months Ended
Mar. 31, 2024
INCOME TAXES  
INCOME TAXES

NOTE 16. INCOME TAXES

Three-Month Periods Ended

March 31, 

($ in thousands)

    

2024

2023

Net Income (loss) before income taxes

$

(10,442)

$

(10,136)

Provision (benefit) for Income

 

 

Effective tax rate

 

0.0

%

 

0.0

%

The Company records income taxes using the asset and liability method. Deferred income tax assets and liabilities are recognized for the future tax effects attributable to temporary differences between the financial statement carrying amounts of existing assets and liabilities and their respective income tax bases, and operating loss and tax credit carryforwards. The Company establishes a valuation allowance if management believes it is more likely than not that the deferred tax assets will not be recovered based on an evaluation of objective verifiable evidence. Management has considered the Company’s history of book and tax income and losses incurred since inception, and the other positive and negative evidence, and has concluded that it is more likely than not that the Company will not realize the benefits of the net deferred tax assets as of March 31, 2024.

As of March 31, 2024, the Company had no unrecognized tax benefits and does not anticipate any significant change to the unrecognized tax benefit balance.

v3.24.1.1.u2
NET LOSS PER COMMON SHARE
3 Months Ended
Mar. 31, 2024
NET LOSS PER COMMON SHARE  
NET LOSS PER COMMON SHARE

NOTE 17. NET LOSS PER COMMON SHARE

The Company accounts for and discloses net earnings (loss) per share using the treasury stock method. Net earnings (loss) per share, or basic earnings (loss) per share, is computed by dividing net earnings (loss) by the weighted-average number of shares of common stock outstanding. Net earnings (loss) per share assuming dilutions, or diluted earnings (loss) per share, is computed by reflecting the potential dilution from the exercise of in-the-money stock options and the issuance of non-vested restricted stock units.

The Company’s basic and diluted weighted-average number of common shares outstanding for the three-month periods ended March 31, 2024 and 2023 were as follows:

Three-Month Periods Ended March 31,

    

2024

    

2023

Basic and diluted

19,757,449

17,807,194

Potentially dilutive securities:

Unvested restricted stock units

 

1,973,395

1,931,969

Stock options

 

1,624,382

1,130,557

Total potentially dilutive securities

3,597,777

3,062,526

The Company’s potentially dilutive securities, including unvested restricted stock and options have been excluded from the computation of diluted loss per share for the three-month periods ended March 31, 2024, and 2023, as the effect would be to reduce the loss per share. Therefore, the weighted average common stock outstanding used to calculate both basic and diluted income loss per share is the same for the three-month periods ended March 31, 2024 and 2023.

v3.24.1.1.u2
BASIS OF PRESENTATION (Policies)
3 Months Ended
Mar. 31, 2024
BASIS OF PRESENTATION  
Basis of Presentation and Principles of Consolidation

Basis of Presentation and Principles of Consolidation

The Company’s consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“GAAP”). The Company’s consolidated financial statements include the accounts of the Company and the accounts of the Company’s wholly-owned subsidiary, JG Pharma, Inc. (“JG” or “JG Pharma”). All intercompany balances and transactions have been eliminated.

Emerging Growth Company

Emerging Growth Company

From time to time, new accounting pronouncements are issued by the Financial Accounting Standards Board (“FASB”) or other standard-setting bodies and adopted by the Company as of the specified effective date. Unless otherwise discussed, the impact of recently issued standards that are not yet effective will not have a material impact on the Company’s audited consolidated financial statements upon adoption. Under the Jumpstart Our Business Startups Act of 2012, as amended, the Company meets the definition of an emerging growth company and elected the extended transition period for complying with new or revised accounting standards, which delays the adoption of these accounting standards until they would apply to private companies.

Use of Estimates

Use of Estimates

The preparation of consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of expenses during the reporting period. Significant estimates made by management include provisions for coupons, chargebacks, wholesaler fees, specialty pharmacy discounts, managed care rebates, product returns, and other allowances customary to the pharmaceutical industry. Significant estimates made by management also include inventory realization, valuation of intangible assets, useful lives of amortizable intangible assets and share-based compensation. Actual results may differ materially and adversely from these estimates. To the extent there are material differences between the estimates and actual results, the Company’s future results of operations will be affected.

Segment Information

Segment Information

Operating segments are defined as components of an enterprise about which separate discrete information is available for evaluation by the chief operating decision maker, or decision-making group, in deciding how to allocate resources and in assessing performance. The Company views its operations and manages its business in one segment, which reflects products for the treatment of dermatological conditions.

v3.24.1.1.u2
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Policies)
3 Months Ended
Mar. 31, 2024
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES  
Accounting Standards Note Yet Adopted

Accounting Standards Note Yet Adopted

In November 2023, the FASB issued Accounting Standards Update (“ASU”) No. 2023-07, Segment Reporting (Topic 280): Improvements to Reportable Segment Disclosures, which requires that an entity report segment information in accordance with Topic 280, Segment Reporting. The amendment in the ASU is intended to improve reportable segment disclosure requirements primarily through enhanced disclosures about significant segment expenses. The amendments in this update are effective for fiscal years beginning after December 15, 2023, and interim periods within fiscal years beginning after December 15, 2024. The Company is currently evaluating the impact of the new standard on its financial statements and disclosures.

In December 2023, the FASB issued ASU No. 2023-09, Income Taxes (Topic 740): Improvements to Income Tax Disclosures, which expands disclosures in an entity’s income tax rate reconciliation table and disclosures regarding cash taxes paid both in the U.S. and foreign jurisdictions. The update will be effective for annual periods beginning after December 15, 2024. The Company is currently evaluating the impact that this guidance will have on its financial statements and disclosures.

v3.24.1.1.u2
INVENTORY (Tables)
3 Months Ended
Mar. 31, 2024
INVENTORY  
Schedule of inventory

    

March 31, 

    

December 31, 

($’s in thousands)

2024

2023

Raw materials

$

4,180

$

4,640

Work-in-process

 

805

 

884

Finished goods

 

5,865

 

4,987

Inventory at cost

10,850

10,511

Inventory reserves

(270)

(305)

Total inventories

$

10,580

$

10,206

v3.24.1.1.u2
INTANGIBLES (Tables)
3 Months Ended
Mar. 31, 2024
INTANGIBLE ASSETS  
Summary of intangible assets

Estimated

Useful Lives

March 31, 

December 31, 

($’s in thousands)

    

(Years)

    

2024

    

2023

Intangible assets - product licenses

  

3-9

$

37,925

$

37,925

Accumulated amortization

(15,309)

(14,495)

Accumulated impairment loss

 

 

(3,143)

 

(3,143)

Total intangible assets

$

19,473

$

20,287

Schedule of future amortization of intangible assets

For the years ended

    

Total Amortization

Remainder of 2024

$

2,443

December 31, 2025

3,257

December 31, 2026

 

2,471

December 31, 2027

 

1,775

December 31, 2028

 

1,595

Thereafter

 

3,990

Subtotal

15,531

Asset not yet placed in service

 

3,942

Total

$

19,473

v3.24.1.1.u2
FAIR VALUE MEASUREMENTS (Tables)
3 Months Ended
Mar. 31, 2024
FAIR VALUE MEASUREMENTS  
Schedule of financial assets and liabilities measured at fair value on a recurring basis

    

 March 31, 2024

($’s in thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

  

  

  

  

Cash and cash equivalents

$

24,057

$

$

$

24,057

Total

$

24,057

$

$

$

24,057

    

 December 31, 2023

($’s in thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

  

  

  

  

Cash and cash equivalents

$

27,439

$

$

$

27,439

Total

$

27,439

$

$

$

27,439

v3.24.1.1.u2
ACCRUED EXPENSES (Tables)
3 Months Ended
Mar. 31, 2024
ACCRUED EXPENSES  
Schedule of accrued expenses

    

March 31, 

    

December 31, 

($’s in thousands)

2024

2023

Accrued expenses:

 

  

 

  

Accrued coupons and rebates

$

7,169

$

9,987

Return reserve

2,806

4,077

Accrued compensation

 

3,599

 

3,374

Accrued royalties payable

1,382

2,015

Accrued legal, accounting and tax

 

335

 

185

Accrued research and development

 

3,034

 

20

Accrued inventory

 

581

 

352

Accrued iPledge program

587

174

Other

 

540

 

166

Total accrued expenses

$

20,033

$

20,350

v3.24.1.1.u2
OPERATING LEASE OBLIGATIONS (Tables)
3 Months Ended
Mar. 31, 2024
OPERATING LEASE OBLIGATIONS  
Schedule of rent expense and quantitative information

The Company recorded lease expense as follows:

    

Three-Month Periods Ended

March 31,

($’s in thousands)

2024

    

2023

Operating lease cost

$

24

$

24

Variable lease cost

 

1

1

Total lease cost

$

25

$

25

The following table summarizes quantitative information about the Company’s operating leases:

    

Three-Month Periods Ended

March 31,

($’s in thousands)

    

2024

2023

Cash paid for amounts included in the measurement of lease liabilities

$

25

$

17

Weighted-average remaining lease term - operating leases

 

0.8

 

1.8

Weighted-average discount rate - operating leases

 

6.25

%

 

6.25

%

Schedule of operating lease liability

As of March 31, 2024, future minimum lease payments under lease agreements associated with the Company’s operations were as follows:

$’s in thousands

    

    

Remainder of 2024

$

77

2025

 

9

Total lease payments

 

86

Less: present value discount

 

(2)

Total operating lease liabilities

$

84

v3.24.1.1.u2
DEBT (Tables)
3 Months Ended
Mar. 31, 2024
DEBT  
Schedule of debt obligation

March 31,

December 31,

($’s in thousands)

    

2024

    

2023

Principal balance

$

15,000

$

15,000

Plus: Exit fee

 

750

 

750

Less: Debt discount and fees

$

(1,066)

$

(1,128)

Net carry amount (Long-term)

$

14,684

$

14,622

Schedule of carrying value of long-term debt

Years ending December 31,

    

Term Loan

Remainder of 2024

$

2025

 

2026

 

4,500

2027

 

11,250

Total

 

15,750

Debt discount

 

(1,066)

Total, net

 

14,684

Current portion

 

Term-loan (long-term)

$

14,684

v3.24.1.1.u2
INTEREST EXPENSE AND FINANCING FEES (Tables)
3 Months Ended
Mar. 31, 2024
INTEREST EXPENSE AND FINANCING FEES  
Schedule of interest expense and financing fees

    

Three-Month Periods Ended March 31,

($’s in thousands)

    

2024

    

2023

Interest payments on term loans and LOC

$

486

$

535

Amortization/Accretion

62

33

Imputed interest on acquired intangible assets

82

Total Interest expense and financing fees

$

548

$

650

v3.24.1.1.u2
SHARE BASED COMPENSATION (Tables)
3 Months Ended
Mar. 31, 2024
SHARE-BASED COMPENSATION  
Summary of components of share-based compensation expense

    

Three-Month Periods Ended March 31,

($’s in thousands)

    

2024

    

2023

Research and development

$

145

$

33

Selling, general and administrative

 

1,261

 

613

Total non-cash compensation expense related to share-based compensation included in operating expense

$

1,406

$

646

Schedule of stock option activities

Weighted

    

    

Weighted

    

    

average

Number

average

Aggregate

remaining

of

exercise

intrinsic

contractual 

    

Shares

    

price

    

value

    

life (years)

Outstanding options at December 31, 2023

2,769,869

$

1.49

$

6,053,833

4.53

Granted

25,000

4.57

Exercised

(55,375)

1.22

Forfeited

(65,523)

2.91

Expired

(1,250)

2.62

Outstanding options at March 31, 2024

 

2,672,721

$

1.49

$

5,866,003

 

4.23

Options vested and exercisable at March 31, 2024

 

1,991,507

$

0.97

$

5,393,973

 

2.73

Schedule of restricted stock units

    

Weighted

Number of

average grant

    

units

    

date Fair value

Unvested balance at December 31, 2023

 

1,306,923

$

3.88

Granted

 

887,500

 

4.97

Vested

(211,028)

3.58

Forfeited

(10,000)

5.02

Unvested balance at March 31, 2024

1,973,395

$

4.40

v3.24.1.1.u2
REVENUES FROM CONTRACTS WITH CUSTOMERS (Tables)
3 Months Ended
Mar. 31, 2024
REVENUES FROM CONTRACTS WITH CUSTOMERS  
Schedule of disaggregation of net revenues

Three-Month Periods Ended March 31, 

($ in thousands)

    

2024

    

2023

Qbrexza®

$

5,017

$

4,094

Accutane®

 

5,819

 

4,648

Amzeeq®

755

1,193

Zilxi®

273

314

Other / legacy

1,166

1,916

Total product revenues

$

13,030

$

12,165

Schedule of other revenue

    

Three-Month Periods Ended March 31,

($in thousands)

2024

2023

Other revenue

 

 

48

Total other revenue

$

$

48

v3.24.1.1.u2
INCOME TAXES (Tables)
3 Months Ended
Mar. 31, 2024
INCOME TAXES  
Schedule of income taxes

Three-Month Periods Ended

March 31, 

($ in thousands)

    

2024

2023

Net Income (loss) before income taxes

$

(10,442)

$

(10,136)

Provision (benefit) for Income

 

 

Effective tax rate

 

0.0

%

 

0.0

%

v3.24.1.1.u2
NET LOSS PER COMMON SHARE (Tables)
3 Months Ended
Mar. 31, 2024
NET LOSS PER COMMON SHARE  
Schedule of basic and diluted weighted-average number of common shares outstanding

Three-Month Periods Ended March 31,

    

2024

    

2023

Basic and diluted

19,757,449

17,807,194

Potentially dilutive securities:

Unvested restricted stock units

 

1,973,395

1,931,969

Stock options

 

1,624,382

1,130,557

Total potentially dilutive securities

3,597,777

3,062,526

v3.24.1.1.u2
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS (Details)
$ in Thousands
3 Months Ended
Dec. 27, 2023
USD ($)
Jan. 26, 2023
USD ($)
shares
Mar. 31, 2024
USD ($)
item
shares
Dec. 31, 2023
USD ($)
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS        
Number of branded drugs in product portfolio | item     7  
Number of authorized generic prescription drugs | item     2  
Cash and cash equivalents     $ 24,057 $ 27,439
Stock issued value     1,484  
Proceeds from issuance of common stock     $ 1,484  
Common Stock        
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS        
Stock issued value   $ 150,000    
Stock issued (in shares) | shares   4,900,000 289,744  
Proceeds from issuance of common stock     $ 1,500  
Common Stock | Employee severance obligation        
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS        
Number of shares available for issuance | shares     3,861,553  
Term loan | East West Bank        
ORGANIZATION AND PLAN OF BUSINESS OPERATIONS        
Maximum borrowing capacity $ 20,000      
Proceeds from term-loan 15,000      
Remaining borrowing capacity $ 5,000      
v3.24.1.1.u2
BASIS OF PRESENTATION - Segment Information (Details)
3 Months Ended
Mar. 31, 2024
segment
BASIS OF PRESENTATION  
Number of operating segment 1
v3.24.1.1.u2
INVENTORY (Details) - USD ($)
$ in Thousands
Mar. 31, 2024
Dec. 31, 2023
INVENTORY    
Raw materials $ 4,180 $ 4,640
Work-in-process 805 884
Finished goods 5,865 4,987
Inventory at cost 10,850 10,511
Inventory reserves (270) (305)
Total Inventories $ 10,580 $ 10,206
v3.24.1.1.u2
INTANGIBLE ASSETS - Intangible assets (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Dec. 31, 2023
INTANGIBLE ASSETS      
Intangible assets - product licenses $ 37,925   $ 37,925
Accumulated Amortization (15,309)   (14,495)
Accumulated impairment loss (3,143)   (3,143)
Total 19,473   $ 20,287
Amortization expense 814 $ 1,069  
Cost of goods sold      
INTANGIBLE ASSETS      
Amortization expense $ 800 $ 1,100  
Minimum      
INTANGIBLE ASSETS      
Estimated Useful Lives (Years) 3 years   3 years
Maximum      
INTANGIBLE ASSETS      
Estimated Useful Lives (Years) 9 years   9 years
v3.24.1.1.u2
INTANGIBLE ASSETS - Future amortization expense (Details) - USD ($)
$ in Thousands
Mar. 31, 2024
Dec. 31, 2023
Future amortization expense    
Remainder of 2024 $ 2,443  
December 31, 2025 3,257  
December 31, 2026 2,471  
December 31, 2027 1,775  
December 31, 2028 1,595  
Thereafter 3,990  
Subtotal 15,531  
Asset not yet placed in service 3,942  
Total $ 19,473 $ 20,287
v3.24.1.1.u2
LICENSES ACQUIRED (Details) - USD ($)
$ in Millions
1 Months Ended
Jun. 30, 2021
Mar. 31, 2021
Jul. 31, 2020
D F D Agreement      
LICENSES ACQUIRED      
Amount payable $ 10.0    
D F D Agreement | Minimum      
LICENSES ACQUIRED      
Percentage of royalties payable on net sales 10.00%    
D F D Agreement | Maximum      
LICENSES ACQUIRED      
Threshold additional contingent regulatory and commercial milestone payments payable $ 155.0    
Percentage of royalties payable on net sales 20.00%    
Asset purchase agreement | Qbrexza      
LICENSES ACQUIRED      
Age of patients   9 years  
Asset purchase agreement | Royalty payment percentage for first two years | Qbrexza      
LICENSES ACQUIRED      
Period of royalty payments   2 years  
Asset purchase agreement | Minimum | Royalty payment percentage for first two years | Qbrexza      
LICENSES ACQUIRED      
Percent of royalty payments   30.00%  
Asset purchase agreement | Minimum | Royalty payment percentage for thereafter | Qbrexza      
LICENSES ACQUIRED      
Percent of royalty payments   12.00%  
Asset purchase agreement | Maximum | Royalty payment percentage for first two years | Qbrexza      
LICENSES ACQUIRED      
Percent of royalty payments   40.00%  
Asset purchase agreement | Maximum | Royalty payment percentage for thereafter | Qbrexza      
LICENSES ACQUIRED      
Percent of royalty payments   19.00%  
Asset purchase agreement | Eli Lilly and Company | Qbrexza      
LICENSES ACQUIRED      
Upfront fees   $ 12.5  
Milestone payments payable   $ 144.0  
License and supply agreement With DRL | Accutane      
LICENSES ACQUIRED      
Amount of expense agreed to pay under the agreement     $ 5.0
Contingent amount payable     $ 17.0
Term of accutane     10 years
Termination accutane agreement period     180 days
v3.24.1.1.u2
FAIR VALUE MEASUREMENTS - Financial assets and liabilities measured at fair value on a recurring basis (Details) - Fair Value, Recurring - USD ($)
$ in Thousands
Mar. 31, 2024
Dec. 31, 2023
Assets:    
Cash and cash equivalents $ 24,057 $ 27,439
Total 24,057 27,439
Level 1    
Assets:    
Cash and cash equivalents 24,057 27,439
Total $ 24,057 $ 27,439
v3.24.1.1.u2
FAIR VALUE MEASUREMENTS - Additional information (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
FAIR VALUE MEASUREMENTS    
Asset transfers, level 2 to 1 $ 0 $ 0
Liability transfers, level 2 to 1 0 0
Transfers in and out of level 3 $ 0 $ 0
v3.24.1.1.u2
RELATED PARTY AGREEMENTS (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Dec. 31, 2023
RELATED PARTY AGREEMENTS      
Due to related party $ 198   $ 195
Shared Services Agreement with Fortress | Fortress      
RELATED PARTY AGREEMENTS      
Service provided by employees of related party 9,361 $ 15,000  
Due to related party $ 200   $ 200
Fortress Income Tax      
RELATED PARTY AGREEMENTS      
Percentage of capital stock requirement to file a combined state tax return 50.00%    
Fortress Income Tax | Fortress      
RELATED PARTY AGREEMENTS      
Equity Method Investment, Ownership Percentage 50.43%    
v3.24.1.1.u2
ACCRUED EXPENSES (Details) - USD ($)
$ in Thousands
Mar. 31, 2024
Dec. 31, 2023
Accrued expenses and other short-term liabilities:    
Accrued coupons and rebates $ 7,169 $ 9,987
Return reserve 2,806 4,077
Accrued compensation 3,599 3,374
Accrued royalties payable 1,382 2,015
Accrued legal, accounting and tax 335 185
Accrued research and development 3,034 20
Accrued inventory 581 352
Accrued iPledge program 587 174
Other 540 166
Total accrued expenses $ 20,033 $ 20,350
v3.24.1.1.u2
OPERATING LEASE OBLIGATIONS (Details)
$ in Millions
1 Months Ended
Sep. 30, 2022
USD ($)
Mar. 31, 2024
ft²
OPERATING LEASE OBLIGATIONS    
Area of property under lease | ft²   3,681
Renewal term 25 months  
Lease annual rate | $ $ 0.1  
v3.24.1.1.u2
OPERATING LEASE OBLIGATIONS - Rent expense (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Lease cost    
Operating lease cost $ 24 $ 24
Variable lease cost 1 1
Total lease cost 25 25
Cash paid for amounts included in the measurement of lease liabilities $ 25 $ 17
Weighted-average remaining lease term - operating leases 9 months 18 days 1 year 9 months 18 days
Weighted-average discount rate - operating leases 6.25% 6.25%
v3.24.1.1.u2
OPERATING LEASE OBLIGATIONS - Future Minimum Lease Payments (Details)
$ in Thousands
Mar. 31, 2024
USD ($)
Future Lease Liability  
Remainder of 2024 $ 77
2025 9
Total lease payments 86
Less: present value discount (2)
Total operating lease liabilities $ 84
v3.24.1.1.u2
DEBT (Details) - USD ($)
$ in Thousands
Mar. 31, 2024
Dec. 31, 2023
DEBT    
Principal balance $ 15,000 $ 15,000
Less: Debt discount and fees (1,066)  
Net carry amount (Long-term) 14,684 14,622
EWB Revolving LOC    
DEBT    
Plus: Exit fee 750 750
EWB Term Loan (Long-term)    
DEBT    
Less: Debt discount and fees $ (1,066) $ (1,128)
v3.24.1.1.u2
DEBT - Additional information (Details) - USD ($)
$ in Thousands
3 Months Ended
Dec. 27, 2023
Mar. 31, 2024
Dec. 31, 2023
DEBT      
Debt instrument, Face value   $ 15,000 $ 15,000
Term loan | East West Bank      
DEBT      
Maximum borrowing capacity $ 20,000    
Amount drawn 15,000    
Remaining borrowing capacity 5,000    
Term loan | SWK Funding LLC      
DEBT      
Amount drawn 15,000    
Remaining borrowing capacity 5,000    
Principal amount of funded term loans   7.50%  
Minimum amount of revenue   $ 70,000  
Principal amount of loan payable   15.00%  
Exit Fees on Percentage of Principal Amount   5.00%  
Loan Processing Fee   $ 200  
Payments of Debt Issuance Costs   $ 200  
Debt Instrument, Interest Rate, Effective Percentage   15.10%  
Outstanding principal balance voluntarily paid off $ 20,000    
Spread on variable rate 7.75%    
Term loan | SWK Funding LLC | Term Loans Prepaid Prior to the First Anniversary of the Closing Date [Member]      
DEBT      
Prepayment premium on percentage of term loan   2.00%  
Term loan | SWK Funding LLC | Term Loans Prepaid Prior On Or After The First Anniversary of the Closing Date [Member]      
DEBT      
Prepayment premium on percentage of term loan   1.00%  
Term loan | SWK Funding LLC | Term Loans Prepaid Thereafter [Member]      
DEBT      
Prepayment premium on percentage of term loan   0.00%  
Term loan | SWK Funding LLC | SOFR      
DEBT      
Floor rate 5.00%    
v3.24.1.1.u2
DEBT - Contractual Maturities of the Long-term debt (Details) - USD ($)
$ in Thousands
Mar. 31, 2024
Dec. 31, 2023
DEBT    
2026 $ 4,500  
2027 11,250  
Total 15,750  
Debt discount (1,066)  
Net carry amount (Long-term) 14,684 $ 14,622
Term-loan (long-term) $ 14,684 $ 14,622
v3.24.1.1.u2
INTEREST EXPENSE AND FINANCING FEES (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
INTEREST EXPENSE AND FINANCING FEES    
Interest payments on term loan and LOC $ 486 $ 535
Amortization/Accretion 62 33
Imputed interest on acquired intangible assets   82
Total Interest expense and financing fees $ 548 $ 650
v3.24.1.1.u2
SHARE-BASED COMPENSATION - 2015 Stock Plan (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
SHARE BASED COMPENSATION    
Share based compensation expense $ 1,406 $ 646
Employee Stock Option    
SHARE BASED COMPENSATION    
Share based compensation expense $ 73,000 $ 200
Stock Plan 2015    
SHARE BASED COMPENSATION    
Increase in number of shares authorized for grant 7,642,857  
Number of shares available for issuance 863,295  
2023 Employee Stock Purchase Plan    
SHARE BASED COMPENSATION    
Increase in number of shares authorized for grant 247,789  
Shares of common stock reserved for future issuance under the plan 300,000  
v3.24.1.1.u2
SHARE-BASED COMPENSATION - Components of share-based compensation expense (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Components of share-based compensation expense    
Total non-cash compensation expense related to share-based compensation included in operating expense $ 1,406 $ 646
Research and development    
Components of share-based compensation expense    
Total non-cash compensation expense related to share-based compensation included in operating expense 145 33
Selling, general and administrative    
Components of share-based compensation expense    
Total non-cash compensation expense related to share-based compensation included in operating expense $ 1,261 $ 613
v3.24.1.1.u2
SHARE-BASED COMPENSATION - Stock Options (Details) - Stock Options - USD ($)
3 Months Ended 12 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Dec. 31, 2023
Number of Shares      
Outstanding options 2,769,869    
Granted 25,000    
Exercised (55,375) 0  
Forfeited (65,523)    
Expired (1,250)    
Outstanding options 2,672,721   2,769,869
Options vested and exercisable at March 31, 2024 1,991,507    
Weighted average exercise price      
Outstanding options - beginning $ 1.49    
Granted 4.57    
Exercised 1.22    
Forfeited 2.91    
Expired 2.62    
Outstanding options - ending 1.49   $ 1.49
Options vested and exercisable at March 31, 2024 $ 0.97    
Average intrinsic value      
Outstanding options at - beginning $ 6,053,833    
Outstanding options - ending 5,866,003   $ 6,053,833
Options vested and exercisable at March 31, 2024 $ 5,393,973    
Weighted average remaining contractual life (year)      
Outstanding options, Weighted average remaining contractual life (years) 4 years 2 months 23 days   4 years 6 months 10 days
Granted 0 years    
Options vested and exercisable at March 31, 2024 2 years 8 months 23 days    
v3.24.1.1.u2
SHARE-BASED COMPENSATION - Restricted Stock Units (Details) - USD ($)
$ / shares in Units, $ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Weighted average grant date Fair value    
Share based compensation expense $ 1,406 $ 646
Restricted stock units    
Number of units    
Unvested balance - beginning 1,306,923  
Granted 887,500  
Vested (211,028) (68,662)
Forfeited (10,000)  
Unvested balance - ending 1,973,395  
Weighted average grant date Fair value    
Unvested balance - beginning $ 3.88  
Granted 4.97  
Vested 3.58  
Forfeited 5.02  
Unvested balance - ending $ 4.40  
Share based compensation expense $ 1,300 $ 500
Number of units issued 211,028 68,662
Aggregate fair market value $ 800 $ 200
Number of unvested shares outstanding 1,973,395  
Unrecognized stock-based compensation expense $ 4,600  
Unrecognized compensation cost expects to recognize over weighted-average period 1 year 7 months 6 days  
v3.24.1.1.u2
SHARE-BASED COMPENSATION - Additional information (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
SHARE BASED COMPENSATION    
Share based compensation expense $ 1,406 $ 646
Proceeds from exercise of stock options 68  
Employee Stock Option    
SHARE BASED COMPENSATION    
Share based compensation expense $ 73,000 $ 200
Exercise of stock options for cash (In shares) 55,375 0
Proceeds from exercise of stock options $ 67,514  
Unrecognized stock-based compensation expense $ 800  
Unrecognized stock-based compensation expense recognition period 1 year 9 months 18 days  
v3.24.1.1.u2
SHARE-BASED COMPENSATION - Employee Stock Purchase Plan (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
SHARE BASED COMPENSATION    
Share based compensation expense $ 1,406 $ 646
Employee Stock Purchase Plan    
SHARE BASED COMPENSATION    
Maximum employee contribution of the eligible earnings 10.00%  
Offering period (in months) 6 months  
Purchase price of common stock (in percent) 85.00%  
Risk-free interest rate 5.20%  
Expected term (years) 6 months  
Expected volatility 98.00%  
Expected dividend yield 0.00%  
Share based compensation expense $ 59,240  
Unrecognized stock-based compensation expense $ 106,110  
v3.24.1.1.u2
REVENUES FROM CONTRACTS WITH CUSTOMERS - Disaggregation of net revenues (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
REVENUES FROM CONTRACTS AND SIGNIFICANT CUSTOMERS    
Total product revenues $ 13,030 $ 12,165
Qbrexza    
REVENUES FROM CONTRACTS AND SIGNIFICANT CUSTOMERS    
Total product revenues 5,017 4,094
Accutane    
REVENUES FROM CONTRACTS AND SIGNIFICANT CUSTOMERS    
Total product revenues 5,819 4,648
Amzeeq    
REVENUES FROM CONTRACTS AND SIGNIFICANT CUSTOMERS    
Total product revenues 755 1,193
Zilxi    
REVENUES FROM CONTRACTS AND SIGNIFICANT CUSTOMERS    
Total product revenues 273 314
Other / legacy    
REVENUES FROM CONTRACTS AND SIGNIFICANT CUSTOMERS    
Total product revenues $ 1,166 $ 1,916
v3.24.1.1.u2
REVENUES FROM CONTRACTS WITH CUSTOMERS - Other revenue (Details)
$ in Thousands
3 Months Ended
Mar. 31, 2023
USD ($)
Other Revenue  
Other revenue $ 48
Other revenue  
Other Revenue  
Other revenue $ 48
v3.24.1.1.u2
REVENUES FROM CONTRACTS WITH CUSTOMERS - Significant customers (Details) - Customer concentration risk - customer
3 Months Ended 12 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Dec. 31, 2023
Product revenue | Customer      
REVENUES FROM CONTRACTS WITH CUSTOMERS      
Number of customers 0 0  
Accounts receivable | One customer      
REVENUES FROM CONTRACTS WITH CUSTOMERS      
Number of customers 1   1
Concentration risk, percentage 14.00%   13.00%
v3.24.1.1.u2
INCOME TAXES (Details) - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
INCOME TAXES    
Net Income (loss) before income taxes $ (10,442) $ (10,136)
Effective tax rate (as a percent) 0.00% 0.00%
Unrecognized tax benefits $ 0  
v3.24.1.1.u2
NET LOSS PER COMMON SHARE (Details) - shares
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Denominator    
Weighted-average shares outstanding - basic 19,757,449 17,807,194
Weighted average shares outstanding - diluted 19,757,449 17,807,194
Dilutive impact from:    
Potentially dilutive securities 3,597,777 3,062,526
Unvested restricted stock units    
Dilutive impact from:    
Potentially dilutive securities 1,973,395 1,931,969
Employee Stock Option    
Dilutive impact from:    
Potentially dilutive securities 1,624,382 1,130,557
v3.24.1.1.u2
Pay vs Performance Disclosure - USD ($)
$ in Thousands
3 Months Ended
Mar. 31, 2024
Mar. 31, 2023
Pay vs Performance Disclosure    
Net Income (Loss) $ (10,442) $ (10,136)
v3.24.1.1.u2
Insider Trading Arrangements
3 Months Ended
Mar. 31, 2024
Trading Arrangements, by Individual  
Rule 10b5-1 Arrangement Adopted false
Non-Rule 10b5-1 Arrangement Adopted false
Rule 10b5-1 Arrangement Terminated false
Non-Rule 10b5-1 Arrangement Terminated false

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