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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
8-K
CURRENT
REPORT
Pursuant
to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date
of report (date of earliest event reported): September 10, 2024
TONIX
PHARMACEUTICALS HOLDING CORP.
(Exact
name of registrant as specified in its charter)
Nevada |
001-36019 |
26-1434750 |
(State
or Other Jurisdiction
of
Incorporation) |
(Commission
File
Number) |
(IRS
Employer
Identification
No.) |
26
Main Street, Chatham, New Jersey 07928
(Address
of principal executive offices) (Zip Code)
Registrant’s
telephone number, including area code: (862) 904-8182
Check
the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under
any of the following provisions (see General Instruction A.2. below):
☐
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
☐
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
☐
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
☐
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
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 |
TNXP |
The NASDAQ Capital Market |
Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405
of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
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. ☐
Item 7.01 |
Regulation
FD Disclosure. |
On September 10, 2024, Tonix Pharmaceuticals Holding Corp. (the “Company”)
announced the appointment of Thomas Englese as Executive Vice President of Commercial Operations, effective immediately. The Company also
provided an update on the timing of the filing of its New Drug Application with the U.S. Food and Drug Administration (“NDA”)
for its TNX-102 SL product candidate for fibromyalgia to October 2024. A copy of the press release which discusses this matter is furnished
hereto as Exhibit 99.01, and incorporated herein by reference.
The
information in this Item 7.01 of this Current Report on Form 8-K, including Exhibit 99.01 attached hereto, shall not be deemed “filed”
for purposes of Section 18 of the United States Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject
to the liabilities of that section, nor shall they be deemed incorporated by reference in any filing under the United States Securities
Act of 1933 or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.
On
September 10, 2024, the Company announced the appointment of Thomas Englese as Executive Vice President of Commercial Operations, effective
immediately. The Company also provided an update on the timing of the filing of its NDA for TNX-102 SL to October 2024.
Forward-
Looking Statements
This
Current Report on Form 8-K contains certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933
and Section 21E of the Securities Exchange Act of 1934 and Private Securities Litigation Reform Act, as amended, including those relating
to the Company’s product development, clinical trials, clinical and regulatory timelines, market opportunity, competitive position,
possible or assumed future results of operations, business strategies, potential growth opportunities and other statement that are predictive
in nature. These forward-looking statements are based on current expectations, estimates, forecasts and projections about the industry
and markets in which we operate and management’s current beliefs and assumptions.
These
statements may be identified by the use of forward-looking expressions, including, but not limited to, “expect,” “anticipate,”
“intend,” “plan,” “believe,” “estimate,” “potential,” “predict,”
“project,” “should,” “would” and similar expressions and the negatives of those terms. These statements
relate to future events or our financial performance and involve known and unknown risks, uncertainties, and other factors which may
cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed
or implied by the forward-looking statements. Such factors include those set forth in the Company’s filings with the SEC. Prospective
investors are cautioned not to place undue reliance on such forward-looking statements, which speak only as of the date of this press
release. The Company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information,
future events or otherwise.
Item 9.01 |
Financial Statements
and Exhibits. |
(d) |
|
Exhibit
No. |
|
Description |
|
|
99.01 |
|
Press Release of the Company, September 10, 2024 |
|
|
104 |
|
Cover
Page Interactive Data File (embedded within the Inline XBRL document) |
SIGNATURE
Pursuant
to the requirement of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the
undersigned thereunto duly authorized.
|
TONIX
PHARMACEUTICALS HOLDING CORP. |
|
|
Date:
September 10, 2024 |
By:
|
/s/
Bradley Saenger |
|
|
|
Bradley
Saenger |
|
|
|
Chief
Financial Officer |
|
|
|
Tonix Pharmaceuticals Holding Corp - 8-K
Exhibit 99.01
Tonix
Pharmaceuticals Announces Appointment of Thomas Englese as Executive Vice President of Commercial Operations
Thomas
brings more than 20 years of commercial and operations experience in the biopharmaceutical industry to Tonix
Tonix
is on track to submit an NDA for TNX-102 SL for fibromyalgia in October of 2024
CHATHAM,
N.J., September 10, 2024 (GLOBE NEWSWIRE) – Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (Tonix or the Company), a biopharmaceutical
company with marketed products and a pipeline of development candidates, today announced the appointment of Thomas (Tom) Englese as Executive
Vice President of Commercial Operations, effective immediately. Mr. Englese brings significant leadership across several functions, including
commercial operations, sales and marketing, and launching and managing major brands through all stages of commercialization.
“Tom
brings extraordinary biopharmaceutical expertise as an industry leader with more than 20 years of commercial experience and a proven
track record of launching and building commercial strategies and executing strategic growth planning,” said Seth Lederman, M.D.,
Chief Executive Officer of Tonix Pharmaceuticals. “We expect to submit the NDA for TNX-102 SL for fibromyalgia, a critical milestone
for this program, in October of this year. Tom will be a valuable addition to Tonix as we advance the fibromyalgia program toward launch,
and further build out our existing commercial and marketing capabilities.”
Mr.
Englese offers breadth and depth of knowledge across numerous therapeutic areas and in different leadership positions. Prior to joining
Tonix, he was the Chief Commercial Officer at Tris Pharmaceuticals, where he managed all commercial aspects of the company and was responsible
for the re-branding, growth, and launch strategies for the ADHD business. Prior to Tris, Mr. Englese was Chief Commercial Officer at
Aziyo Biologics where he set the strategic direction for the commercial organization for a diverse range of therapeutic businesses. Previously,
Mr. Englese spent 11 years in various roles at Mallinckrodt PLC (formerly Ikaria Inc.), culminating in serving as the Senior Vice President
and General Manager of North America Hospital Therapies. At Mallinckrodt, he was responsible for setting strategic direction and objectives
to ensure alignment to corporate objectives for a +$1 billion North America franchise, and was accountable for the launch teams for several
new products. Mr. Englese holds a Master of Business Administration in Finance from Pennsylvania State University and a Bachelor of Science
in Marketing with a Minor in Communications from Villanova University. Mr. Englese succeeds the Company’s current EVP, Commercial
Operations, Jim Hunter, who is stepping down to pursue retirement.
“I
am excited to join Tonix at this important point in the Company’s growth,” said Mr. Englese. “I look forward to working
with the Tonix leadership team to advance TNX-102 SL and if approved, help bring it to patients who could benefit from its differentiated
activity and profile.”
Tonix
Pharmaceuticals Holding Corp.*
Tonix
is a fully integrated biopharmaceutical company focused on transforming therapies for pain management and modernizing solutions for public
health challenges. Tonix’s development portfolio is focused on central nervous system (CNS) disorders, and its priority is to submit
a New Drug Application (NDA) to the FDA in October of 2024 for TNX-102 SL, a product candidate for which two statistically significant
Phase 3 studies have been completed for the management of fibromyalgia. The FDA has granted Fast Track designation to TNX-102 SL for
the management of fibromyalgia. TNX-102 SL is also being developed to treat acute stress reaction. Tonix’s CNS portfolio includes
TNX-1300 (cocaine esterase), a biologic in Phase 2 development designed to treat cocaine intoxication that has Breakthrough Therapy designation.
Tonix’s immunology development portfolio consists of biologics to address organ transplant rejection, autoimmunity and cancer,
including TNX-1500, which is a humanized monoclonal antibody targeting CD40-ligand (CD40L or CD154) being developed for the prevention
of allograft rejection and for the treatment of autoimmune diseases. Tonix also has product candidates in development in the areas of
rare disease, including TNX-2900 for Prader-Willi syndrome, and infectious disease, including a vaccine for mpox, TNX-801. Tonix recently
announced the U.S. Department of Defense (DoD), Defense Threat Reduction Agency (DTRA) awarded it a contract for up to $34 million over
five years in an Other Transaction Agreement (OTA) to develop TNX-4200, small molecule broad-spectrum antiviral agents targeting CD45
for the prevention or treatment of infections to improve the medical readiness of military personnel in biological threat environments.
Tonix owns and operates a state-of-the art infectious disease research facility in Frederick, MD, instrumental in progressing this development.
Tonix Medicines, our commercial subsidiary, markets Zembrace® SymTouch® (sumatriptan injection)
3 mg and Tosymra® (sumatriptan nasal spray) 10 mg for the treatment of acute migraine with or without aura in adults.
*Tonix’s
product development candidates are investigational new drugs or biologics and have not been approved for any indication.
Zembrace
SymTouch and Tosymra are registered trademarks of Tonix Medicines.
This
press release and further information about Tonix can be found at www.tonixpharma.com.
Forward
Looking Statements
Certain
statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. These
statements may be identified by the use of forward-looking words such as “anticipate,” “believe,” “forecast,”
“estimate,” “expect,” and “intend,” among others. These forward-looking statements are based on Tonix's
current expectations and actual results could differ materially. There are a number of factors that could cause actual events to differ
materially from those indicated by such forward-looking statements. These factors include, but are not limited to, risks related to the
failure to obtain FDA clearances or approvals and noncompliance with FDA regulations; risks related to the failure to successfully market
any of our products; risks related to the timing and progress of clinical development of our product candidates; our need for additional
financing; uncertainties of patent protection and litigation; uncertainties of government or third party payor reimbursement; limited
research and development efforts and dependence upon third parties; and substantial competition. As with any pharmaceutical under development,
there are significant risks in the development, regulatory approval and commercialization of new products. Tonix does not undertake an
obligation to update or revise any forward-looking statement. Investors should read the risk factors set forth in the Annual Report on
Form 10-K for the year ended December 31, 2023, as filed with the Securities and Exchange Commission (the “SEC”) on April
1, 2024, and periodic reports filed with the SEC on or after the date thereof. All of Tonix's forward-looking statements are expressly
qualified by all such risk factors and other cautionary statements. The information set forth herein speaks only as of the date thereof.
Tonix
Pharmaceuticals Investor Contact
Jessica
Morris
Tonix
Pharmaceuticals
investor.relations@tonixpharma.com
(862)
904-8182
Peter
Vozzo
ICR
Westwicke
peter.vozzo@westwicke.com
(443)
213-0505
Tonix
Pharmaceuticals Media Contact
Ray
Jordan
Putnam
Insights
ray@putnaminsights.com
(949)
245-5432
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Grafico Azioni Tonix Pharmaceuticals (NASDAQ:TNXP)
Storico
Da Dic 2024 a Gen 2025
Grafico Azioni Tonix Pharmaceuticals (NASDAQ:TNXP)
Storico
Da Gen 2024 a Gen 2025