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Warrants [Member]
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
March 25, 2025
Date of Report (Date of earliest event reported)
Zura
Bio Limited
(Exact name of registrant as specified in its charter)
Cayman Islands |
|
001-40598 |
|
98-1725736 |
(State or other jurisdiction of
incorporation) |
|
(Commission
File Number) |
|
(I.R.S. Employer
Identification No.) |
1489 W. Warm Springs Rd. #110
Henderson, NV 89014
(Address of principal executive
offices,
including zip code)
(702) 825-9872
(Registrant’s telephone
number, including area code)
(Former name or former address,
if changed since last report)
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:
¨ | Written
communication 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 |
Class A Ordinary Shares, par value $0.0001 per share |
|
ZURA |
|
The Nasdaq Stock 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 x
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 2.02. | Results of Operations and Financial Condition. |
On March 25, 2025,
Zura Bio Limited (“ZURA”, the “Company”) issued a press release announcing its 2024
full fiscal year financial results. A copy of the press release is furnished herewith as Exhibit 99.1 and incorporated herein by reference.
The information
in this Item 2.02 shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, nor shall
it be deemed incorporated by reference in any Company filing under the Securities Act of 1933 or the Securities Exchange Act of 1934,
except as shall be expressly set forth by specific reference in such filing.
| Item 9.01. | Financial Statements and Exhibits |
(d) Exhibits.
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934,
the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
|
ZURA BIO LIMITED |
|
|
Date: March 25, 2025 |
By: |
/s/ Kim Davis |
|
|
Kim Davis |
|
|
Chief Legal Officer |
Exhibit 99.1
Zura Bio Reports Full Year 2024 Financial Results
and Recent Corporate Updates
| · | Achieved
key milestones in 2024 that enhanced our leadership team, strengthened our financial position,
and progressed our clinical pipeline |
| · | Initiated
the Phase 2 TibuSURE trial in adults with systemic sclerosis (SSc) |
| · | Completed
a $112.5 million private placement financing in April 2024, contributing to a total of $176.5
million in cash and cash equivalents, as of December 31, 2024 |
| · | Cash
runway anticipated through 2027, supporting operations and funding anticipated tibulizumab
data readouts in SSc and hidradenitis suppurativa (HS) |
HENDERSON, Nev. – (BUSINESS WIRE) – March 25, 2025 –
Zura Bio Limited (Nasdaq: ZURA) (“Zura Bio” or the “Company”), a clinical stage, multi-asset immunology
company developing novel dual-pathway antibodies for autoimmune and inflammatory diseases, today reported full year 2024 financial results
and recent corporate updates.
“In 2024, we reached key milestones that reinforced our financial
foundation, expanded our leadership team, and advanced our clinical pipeline, highlighting our commitment to establishing a leading presence
in immunology,” said Robert Lisicki, Chief Executive Officer of Zura Bio. “We remain dedicated to developing treatments for
patients with severe autoimmune and inflammatory diseases. In 2025, we look forward to building on this progress with continued advancements,
including our TibuSURE Phase 2 study for SSc and the anticipated launch of a Phase 2 study for HS in Q2.”
CORPORATE HIGHLIGHTS AND UPCOMING ANTICIPATED MILESTONES
Tibulizumab
Systemic sclerosis
In December 2024, Zura Bio advanced its clinical pipeline by initiating
the Phase 2 TibuSURE trial in SSc.
Hidradenitis suppurativa
| · | In
September 2024, a third-party Contract Research Organization was selected to oversee and
conduct the Phase 2 clinical program for HS. |
| · | Zura Bio holds an active Investigational New Drug with the U.S. Food
and Drug Administration, allowing the clinical trial to proceed. |
| · | Zura
Bio plans to initiate a Phase 2 trial for the treatment of adults with HS in the second quarter
of 2025. |
Crebankitug
| · | Zura
Bio is exploring potential therapeutic applications where IL-7/TSLP inhibition may provide
meaningful clinical and commercial benefits. |
| · | Ongoing
translational medicine research and collaborations with key opinion leaders aim to enhance
the understanding of its clinical potential. |
Torudokimab
Zura Bio is monitoring external Phase 2 and Phase 3 IL-33/ST2 data
in asthma and chronic obstructive pulmonary disease to inform its development strategy.
Corporate Highlights
| · | In
January 2024, Kiran Nistala, MBBS, PhD, a rheumatologist and immunologist, joined as Chief
Medical Officer and Head of Development, further strengthening our clinical and scientific
leadership. |
| · | In
April 2024, Robert Lisicki was appointed Chief Executive Officer and played a key role in
securing $112.5 million through an oversubscribed private placement, supported by leading
life sciences-focused institutional investors. |
| · | In
June 2024, a Scientific Advisory Board was established, composed of leading specialists in
rheumatology, dermatology, and immunology. |
| · | In
June 2024, data from two abstracts on tibulizumab in Sjögren’s syndrome and rheumatoid
arthritis were presented at the Annual European Congress of Rheumatology. |
| · | In
August 2024, the Company successfully completed a warrant exchange, simplifying its capital
structure. |
| · | In
September 2024, the Company established an "at-the-market" (ATM) program, providing
increased financial flexibility. |
FULL YEAR 2024 FINANCIAL RESULTS
Cash Position
Cash and cash equivalents were $176.5 million as of December
31, 2024, as compared to $99.8 million as of December 31, 2023. Zura Bio anticipates that its existing cash and cash equivalents
should be sufficient to support operations as currently planned through 2027.
Research and Development (R&D) Expenses
Research and development expenses were $24.4 million for the year
ended December 31, 2024, a decrease of $19.6 million compared to $44.0 million for the year ended December 31, 2023. The decrease was
primarily due to $27.2 million related to the acquisition of tibulizumab from Eli Lilly and Company (“Lilly”) during the
year ended December 31, 2023. This decrease was partially offset by a $4.5 million milestone payment in 2024 related to the Lilly license
for tibulizumab and an increase of $2.9 million for cash-based compensation expenses for personnel in R&D functions and an increase
of $2.0 million of costs incurred for consulting services for our product candidates.
General and Administrative (G&A) Expenses
General and administrative expenses were $30.8 million for the
year ended December 31, 2024, an increase of $12.2 million compared to $18.6 million for the year ended December 31, 2023.
The increase was primarily due to $8.3 million in compensation costs, including a one-time non-cash stock-based compensation expense
of $5.9 million and a $2.4 million increase in cash and non-cash compensation costs for personnel in executive and administrative functions,
as well as a $2.9 million increase in professional fees, driven by $1.6 million in fees related to the warrant exchange.
Net Loss
Net Loss was $45.4 million or $0.60 per share for the year ended December
31, 2024, compared to $69.2 million or $2.09 per share for the year ended December 31, 2023.
ABOUT ZURA BIO
Zura Bio is a clinical-stage, multi-asset immunology company developing
novel dual-pathway antibodies for autoimmune and inflammatory diseases. Currently, Zura Bio is developing three assets which have completed
Phase 1/1b studies. The company is developing a portfolio of therapeutic indications for tibulizumab (ZB-106), crebankitug (ZB-168),
and torudokimab (ZB-880), with a goal of demonstrating their efficacy, safety, and dosing convenience in autoimmune and inflammatory
diseases, including systemic sclerosis and other indications with unmet needs.
FORWARD-LOOKING STATEMENTS
This communication includes “forward-looking statements”
within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Words such as
“expect,” “estimate,” “project,” “budget,” “forecast,” “anticipate,”
“intend,” “plan,” “may,” “will,” “could,” “should,” “believe,”
“predict,” “potential,” “continue,” “strategy,” “future,” “opportunity,”
“would,” “seem,” “seek,” “outlook,” “goal,” “mission,” and similar
expressions are intended to identify such forward-looking statements. Forward-looking statements are predictions, projections and other
statements about future events that are based on current expectations and assumptions and, as a result, are subject to risks and uncertainties
that could cause the actual results to differ materially from the expected results. These statements are based on various assumptions,
whether or not identified in this communication. These forward-looking statements in this release include, but are not limited to, statements
regarding: Zura Bio’s forecasts, including with respect to its cash resources; Zura Bio’s expectations regarding funding,
operating and working capital expenditures, business strategies and objectives; ; expectations with respect to Zura Bio’s development
program, including its product candidates and the potential benefits thereof, data readouts, regulatory matters, clinical trials and
the design and timing thereof; expectations with respect to development programs, data readouts and product candidates of other parties.
These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied
on by an investor as, a guarantee, an assurance, a prediction or a definitive statement of fact or probability.
Actual events are difficult or impossible to predict and could differ
materially from those expressed or implied in such forward-looking statements, as a result of these risks and uncertainties, which include,
but are not limited to: Zura Bio’s expectations regarding its product candidates and their related benefits, and Zura Bio’s
beliefs regarding competing product candidates and products both in development and approved, may not be achieved; Zura Bio's vision
and strategy may not be successful; the timing of key events and initiation of Zura Bio's studies, regulatory matters and release of
clinical data may take longer than anticipated or may not be achieved at all; the potential general acceptability and maintenance of
Zura Bio's product candidates by regulatory authorities, payors, physicians, and patients may not be achieved; Zura Bio's ability to
attract and retain key personnel; Zura Bio's expectations with respect to its future operating expenses, capital requirements and needs
for additional financing may not be achieved; Zura Bio has not completed any clinical trials, and has no products approved for commercial
sale; Zura Bio has incurred significant losses since inception, and expects to incur significant losses for the foreseeable future and
may not be able to achieve or sustain profitability in the future; Zura Bio requires substantial additional capital to finance its operations,
and if it is unable to raise such capital when needed or on acceptable terms, Zura Bio may be forced to delay, reduce, and/or eliminate
one or more of its development programs or future commercialization efforts; Zura Bio may be unable to renew existing contracts or enter
into new contracts; Zura Bio relies on third-party contract development manufacturing organizations for the manufacture of clinical materials;
Zura Bio relies on contract research organizations, clinical trial sites, and other third parties to conduct of its preclinical studies
and clinical trials; Zura Bio may be unable to obtain regulatory approval for its product candidates, and there may be related restrictions
or limitations of any approved products; Zura Bio may be unable to successfully respond to general economic and geopolitical conditions;
Zura Bio may be unable to effectively manage growth; Zura Bio faces competitive pressures from other companies worldwide; Zura Bio may
be unable to adequately protect its intellectual property rights; and other factors set forth in documents filed, or to be filed by Zura
Bio, with the Securities and Exchange Commission (SEC), including the risks and uncertainties described in the “Risk Factors”
section of Zura Bio's Annual Report on Form 10-K for the year ended December 31, 2024 and other filings with the SEC. These risks and
uncertainties may be amplified by health epidemics or other unanticipated global disruption events, which may continue to cause economic
uncertainty. Zura Bio cautions that the foregoing list of factors is not exclusive or exhaustive and not to place undue reliance upon
any forward-looking statements, which speak only as of the date made. Zura Bio gives no assurance that it will achieve its expectations.
Zura Bio does not undertake or accept any obligation to update any forward-looking statements, except as required by law.
ZURA BIO LIMITED
CONSOLIDATED BALANCE SHEETS
(In thousands, except share data)
| |
December 31, | |
| |
2024 | | |
2023 | |
Assets | |
| | | |
| | |
Current assets | |
| | | |
| | |
Cash and cash equivalents | |
$ | 176,498 | | |
$ | 99,806 | |
Prepaid expenses and other current assets | |
| 2,246 | | |
| 1,037 | |
Total current assets | |
| 178,744 | | |
| 100,843 | |
Property and equipment, net | |
| 91 | | |
| – | |
Other assets | |
| 698 | | |
| – | |
Total assets | |
$ | 179,533 | | |
$ | 100,843 | |
| |
| | | |
| | |
Liabilities, Redeemable Noncontrolling Interest and Shareholders' Equity | |
| | | |
| | |
Current liabilities | |
| | | |
| | |
Accounts payable and accrued expenses | |
$ | 19,514 | | |
$ | 20,302 | |
Total current liabilities | |
| 19,514 | | |
| 20,302 | |
Private placement warrants | |
| – | | |
| 990 | |
Total liabilities | |
| 19,514 | | |
| 21,292 | |
| |
| | | |
| | |
Commitments and contingencies | |
| | | |
| | |
| |
| | | |
| | |
Redeemable noncontrolling interest | |
| 11,663 | | |
| 18,680 | |
| |
| | | |
| | |
Shareholders’ Equity | |
| | | |
| | |
Preferred shares, $0.0001 par value, 1,000,000 authorized as of December 31, 2024 and 2023; no shares issued and outstanding as of December 31, 2024 and 2023 | |
| – | | |
| – | |
Class A Ordinary Shares, $0.0001 par value; 300,000,000 shares authorized as of December 31, 2024, and 2023; 65,297,530 and 43,593,678 shares issued and outstanding as of December 31, 2024 and 2023, respectively | |
| 7 | | |
| 4 | |
Additional paid-in capital | |
| 302,705 | | |
| 162,820 | |
Accumulated deficit | |
| (155,897 | ) | |
| (103,494 | ) |
Total Zura Bio Limited shareholders' equity | |
| 146,815 | | |
| 59,330 | |
Noncontrolling interest | |
| 1,541 | | |
| 1,541 | |
Total shareholders’ equity | |
| 148,356 | | |
| 60,871 | |
Total liabilities, redeemable noncontrolling interest and shareholders' equity | |
$ | 179,533 | | |
$ | 100,843 | |
ZURA BIO LIMITED
CONSOLIDATED STATEMENTS OF OPERATIONS
(In thousands, except share and per share data)
| |
For the Years Ended December 31, | |
| |
2024 | | |
2023 | |
Operating expenses: | |
| | | |
| | |
Research and development | |
$ | 24,401 | | |
$ | 43,999 | |
General and administrative | |
| 30,788 | | |
| 18,639 | |
Total operating expenses | |
| 55,189 | | |
| 62,638 | |
Loss from operations | |
| (55,189 | ) | |
| (62,638 | ) |
Other (income)/expense, net | |
| | | |
| | |
Interest income | |
| (7,998 | ) | |
| (2,186 | ) |
Change in fair value of private placement warrants | |
| 5,240 | | |
| (724 | ) |
Change in fair value of note payable | |
| – | | |
| 2,244 | |
Dividend income | |
| – | | |
| (1,392 | ) |
Other income, net | |
| (28 | ) | |
| (17 | ) |
Total other income, net | |
| (2,786 | ) | |
| (2,075 | ) |
Loss before income taxes | |
| (52,403 | ) | |
| (60,563 | ) |
Income tax benefit | |
| – | | |
| – | |
Net loss before redeemable noncontrolling interest | |
| (52,403 | ) | |
| (60,563 | ) |
Net loss attributable to redeemable noncontrolling interest | |
| – | | |
| 203 | |
Net loss | |
| (52,403 | ) | |
| (60,360 | ) |
Adjustment of redeemable noncontrolling interest from redemption value to carrying value | |
| 7,017 | | |
| – | |
Accretion of redeemable noncontrolling interest to redemption value | |
| – | | |
| (7,220 | ) |
Deemed contribution from redeemable noncontrolling interest | |
| – | | |
| 9,212 | |
Deemed dividend to redeemable noncontrolling interest | |
| – | | |
| (10,875 | ) |
Net loss attributable to Class A Ordinary Shareholders of Zura | |
$ | (45,386 | ) | |
$ | (69,243 | ) |
Net loss per share attributable to Class A Ordinary Shareholders of Zura, basic and diluted | |
$ | (0.60 | ) | |
$ | (2.09 | ) |
Weighted-average Class A Ordinary Shares used in computing net loss per share attributable to Class A Ordinary Shareholders of Zura, basic and diluted | |
| 75,070,761 | | |
| 33,064,036 | |
CONTACTS
Megan K. Weinshank
Head of Corporate Affairs
ir@zurabio.com
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Grafico Azioni Zura Bio (NASDAQ:ZURA)
Storico
Da Mar 2025 a Mar 2025
Grafico Azioni Zura Bio (NASDAQ:ZURA)
Storico
Da Mar 2024 a Mar 2025