ZyVersa Therapeutics, Inc. (Nasdaq: ZVSA, or "ZyVersa"), a
clinical-stage specialty biopharmaceutical company developing
first-in-class drug candidates for the treatment of renal and
inflammatory diseases with high unmet medical needs, today provides
a corporate update and reported financial results for the fourth
quarter and full year ended December 31, 2022.
“This is a very exciting time in the growth and evolution of
ZyVersa. We seek to create shareholder value through the
development of first-in-class drugs at the forefront of innovation
for renal and inflammatory diseases,” said Stephen C. Glover,
Co-founder, Chairman, Chief Executive Officer, and President of
ZyVersa. “We are currently advancing a dynamic pipeline of drug
candidates with multiple programs built around our two proprietary
technologies – Cholesterol Efflux Mediator™ VAR 200 for treatment
of kidney diseases, and inflammasome ASC inhibitor IC 100 for
treatment of multiple CNS and other inflammatory diseases. We
believe that both technologies have transformative potential,
enabling ZyVersa to target numerous, underserved disease
indications.”
Mr. Glover continued: “Our lead clinical product candidate,
Cholesterol Efflux Mediator™ VAR 200 is being developed for
potential treatment of multiple renal indications including FSGS, a
progressive form of kidney disease for which no approved
disease-specific treatment options exist. An investigator-initiated
trial to evaluate VAR 200 in up to three renal indications
including FSGS, is expected to initiate in the fourth quarter of
2023. Additionally, ZyVersa plans to complete IC 100’s preclinical
program this year, with an Investigational New Drug (“IND”)
submission anticipated in second quarter of 2024.”
Mr. Glover concluded: “We believe that 2023 offers the potential
to be a year of significant progress at ZyVersa based on the
value-building milestones that we expect to achieve over the next
12 to 18 months. Our leadership team and Board members are focused
on executing our business and clinical development strategy
designed to position ZyVersa as a leading and innovative company
developing transformative drugs for underserved patients with renal
and inflammatory diseases.”
FOURTH QUARTER AND RECENT PROGRAM UPDATES
Phase 2a-Ready Cholesterol Efflux
Mediator™ VAR 200 Targeting Renal
Disease
- Planning investigator-initiated
trial (“IIT”) with nephrologists in up to three renal indications,
including FSGS, with trial initiation expected in the fourth
quarter of 2023. Data from the IIT is expected to validate FSGS as
the lead indication and will guide protocol development for a Phase
2a clinical trial
- Added three members to ZyVersa’s
Renal Scientific Advisory Board
Inflammasome ASC Inhibitor IC 100: Blocks Initiation and
Perpetuation of Damaging Inflammation Associated with Multiple
Sclerosis and CNS and Other Inflammatory Diseases
- Preparing to complete IND-enabling
preclinical studies by end of year, with the goal of filing an IND
application with the U.S. Food and Drug Administration in the
second quarter of 2024
- Plan to expand research program
beyond proof-of-concept for multiple sclerosis and acute
respiratory distress syndrome to evaluate additional
indications
- Completed initial toxicology studies
with IC 100 in rodents and non-human primates demonstrating no
significant safety issues at doses up to 300mg/kg
- Awarded a grant from The Michael J.
Fox Foundation to determine if IC 100 inhibition of microglial
inflammasome activation in a Parkinson’s disease (“PD”) model
blocks neuroinflammation driving PD pathology
- The research is underway at the
University of Miami Miller School of Medicine in the labs of IC 100
inventors, Drs. Robert W. Keane and Juan Pablo de Rivero
Vaccari
- Researchers at the University of
Miami Miller School of Medicine published two peer-reviewed papers
in Translational Research:
- The first demonstrates that IC 100 gains access into cells,
binds to ASC, and alters the structure of ASC specks, inhibiting
activation and release of IL-1β to attenuate heightened
inflammation associated with disease
- The second indicates that IC 100 reduces CNS inflammasome
activation in a mouse model for Alzheimer’s disease following
traumatic brain injury
- Those researchers also published a
third peer-reviewed paper in Frontiers in Molecular Neuroscience
which showed that IC 100 reduces brain inflammation in an aging
mouse model
Closed Business Combination with Larkspur Health
Acquisition Corp. and Began Trading on the Nasdaq Global
Market
- Completed business combination with
Larkspur Health Acquisition Corp., a blank-check special purpose
acquisition company, in December 2022
- Initiated trading on the Nasdaq
Global Market under the ticker symbol “ZVSA” on December 13,
2022
Mr. Glover commented: “Our business combination with Larkspur
Health Acquisition Corp in December was a major inflection point
for ZyVersa, providing a gateway to the Nasdaq Global Market, which
we believe will serve to increase long-term shareholder value by
augmenting our visibility and broadening our engagement with
investors, further enabling our R&D initiatives. It was the
culmination of several months of hard work by our executive team
during a very challenging period for the capital markets and
biotechnology industry. We believe that our ability to complete the
deal is a testimony to senior management’s deep biopharma
experience, and the tenacity and creativity we bring to ZyVersa
every day.”
FOURTH QUARTER AND YEAR END 2022 FINANCIAL
RESULTS
Since its inception in 2014 through December 31, 2022, ZyVersa
has not generated any revenue and has incurred significant
operating losses and negative cash flows from its operations. Based
on its current operating plan, ZyVersa expects its cash of $5.9
million as of December 31, 2022 will be sufficient to fund its
operating expenses and capital expenditure requirements on a
month-to-month basis. ZyVersa will need additional financing to
support its continuing operations. ZyVersa will seek to fund its
operations through public or private equity or debt financings or
other sources, which may include government grants and
collaborations with third parties.
Research and development expenses were $0.4 million for the
period from December 13, 2022, through December 31, 2022 (the
“Successor” period) and $5.4 million for the period from
January 1, 2022 through December 12, 2022 (the “Predecessor”
period). Research and development expenses for the combined year
ended December 31, 2022 were $5.8 million, an increase of $3.7
million or 173.4% from the $2.1 million for the Predecessor year
ended December 31, 2021. The increase in research and development
expenses was due to an overall increase in spending for batch
manufacturing, analytical services, and for materials supplies for
manufacturing.
General and administrative expenses were $0.4 million for the
Successor period and $7.6 million for the Predecessor period.
General and administrative expenses for the combined year ended
December 31, 2022, were $8.0 million, an increase of $2.4 million
or 43.8% from the $5.6 million for the Predecessor year ended
December 31, 2021. The increase in general and administrative
expenses is primarily due to transaction costs of $2.2 million
directly related to preparations for the business
combination.
Net losses were $75,018 for the Successor period and $14.0
million for the Predecessor period. Net loss for the combined year
ended December 31, 2022 was $14.1 million, an increase of $6.0
million or 75% from the $8.1 million for the Predecessor year ended
December 31, 2021. As noted above, the increase is primarily driven
by manufacturing costs for research and development ($3.7 million)
and general and administrative costs ($2.4 million) primarily
related to transaction costs for the business combination.
About ZyVersa Therapeutics, Inc.
ZyVersa (Nasdaq: ZVSA) is a clinical stage specialty
biopharmaceutical company leveraging advanced, proprietary
technologies to develop first-in-class drugs for patients with
renal and inflammatory diseases who have significant unmet medical
needs. The Company is currently advancing a therapeutic development
pipeline with multiple programs built around its two proprietary
technologies – Cholesterol Efflux Mediator™ VAR 200 for
treatment of kidney diseases, and IC 100, a novel inflammasome ASC
inhibitor to control damaging inflammation associated with numerous
CNS and other inflammatory diseases. For more information, please
visit www.zyversa.com.
Cautionary Statement Regarding Forward-Looking
Statements
Certain statements contained in this press release regarding
matters that are not historical facts, are forward-looking
statements within the meaning of Section 21E of the Securities
Exchange Act of 1934, as amended, and the Private Securities
Litigation Reform Act of 1995. These include statements regarding
management’s intentions, plans, beliefs, expectations, or forecasts
for the future, and, therefore, you are cautioned not to place
undue reliance on them. No forward-looking statement can be
guaranteed, and actual results may differ materially from those
projected. ZyVersa uses words such as “anticipates,” “believes,”
“plans,” “expects,” “projects,” “future,” “intends,” “may,” “will,”
“should,” “could,” “estimates,” “predicts,” “potential,”
“continue,” “guidance,” and similar expressions to identify these
forward-looking statements that are intended to be covered by the
safe-harbor provisions. Such forward-looking statements are based
on ZyVersa’s expectations and involve risks and uncertainties;
consequently, actual results may differ materially from those
expressed or implied in the statements due to a number of factors,
including ZyVersa’s plans to develop and commercialize its product
candidates, the timing of initiation of ZyVersa’s planned
preclinical and clinical trials; the timing of the availability of
data from ZyVersa’s preclinical and clinical trials; the timing of
any planned investigational new drug application or new drug
application; ZyVersa’s plans to research, develop, and
commercialize its current and future product candidates; the
clinical utility, potential benefits and market acceptance of
ZyVersa’s product candidates; ZyVersa’s commercialization,
marketing and manufacturing capabilities and strategy; ZyVersa’s
ability to protect its intellectual property position; and
ZyVersa’s estimates regarding future revenue, expenses, capital
requirements and need for additional financing.
New factors emerge from time-to-time, and it is not possible for
ZyVersa to predict all such factors, nor can ZyVersa assess the
impact of each such factor on the business or the extent to which
any factor, or combination of factors, may cause actual results to
differ materially from those contained in any forward-looking
statements. Forward-looking statements included in this press
release are based on information available to ZyVersa as of the
date of this press release. ZyVersa disclaims any obligation to
update such forward-looking statements to reflect events or
circumstances after the date of this press release, except as
required by applicable law.
This press release does not constitute an offer to sell, or the
solicitation of an offer to buy, any securities.
Corporate and IR Contact:Karen CashmereChief
Commercial
Officerkcashmere@zyversa.com786-251-9641
Media ContactsTiberend Strategic
Advisors, Inc.Casey
McDonaldcmcdonald@tiberend.com646-577-8520
Dave Schemeliadschemelia@tiberend.com609-468-9325
|
ZYVERSA
THERAPEUTICS, INC. |
CONDENSED
CONSOLIDATED BALANCE SHEETS |
|
|
|
|
|
|
|
|
|
Successor |
|
|
Predecessor |
|
|
December 31, 2022 |
|
|
December 31, 2021 |
ASSETS |
|
|
|
|
|
Current assets: |
|
|
|
|
|
Cash and cash equivalents |
|
$ |
5,902,199 |
|
|
|
$ |
328,581 |
|
Prepaid and other current assets |
|
|
460,347 |
|
|
|
|
483,201 |
|
Total current assets |
|
|
6,362,546 |
|
|
|
|
811,782 |
|
|
|
|
|
|
|
Property and equipment, net |
|
|
17,333 |
|
|
|
|
27,733 |
|
In-process research and development |
|
|
100,086,329 |
|
|
|
|
- |
|
Goodwill |
|
|
11,895,033 |
|
|
|
|
- |
|
Operating lease right-of-use asset |
|
|
98,371 |
|
|
|
|
- |
|
Other assets |
|
|
46,659 |
|
|
|
|
286,659 |
|
Total assets |
|
$ |
118,506,271 |
|
|
|
$ |
1,126,174 |
|
|
|
|
|
|
|
LIABILITIES, TEMPORARY EQUITY AND STOCKHOLDERS' EQUITY
(DEFICIENCY) |
|
|
|
Current liabilities: |
|
|
|
|
|
Accounts payable |
|
$ |
6,025,645 |
|
|
|
$ |
2,000,100 |
|
Accrued expenses and other current liabilities |
|
|
2,053,559 |
|
|
|
|
1,914,101 |
|
Operating lease liability |
|
|
108,756 |
|
|
|
|
- |
|
Derivative liabilities |
|
|
- |
|
|
|
|
560,600 |
|
Convertible notes payable |
|
|
- |
|
|
|
|
9,151,508 |
|
Total current liabilities |
|
|
8,187,960 |
|
|
|
|
13,626,309 |
|
|
|
|
|
|
|
Deferred tax liability |
|
|
10,323,983 |
|
|
|
|
- |
|
Total liabilities |
|
|
18,511,943 |
|
|
|
|
13,626,309 |
|
|
|
|
|
|
|
Commitments and contingencies |
|
|
|
|
|
Successor redeemable common stock, subject to possible
redemption, |
|
|
|
|
65,783 shares outstanding as of December 31, 2022 |
|
|
331,331 |
|
|
|
|
- |
|
Predecessor redeemable common stock, subject to possible
redemption, |
|
|
|
|
331,331 shares outstanding as of December 31, 2021 |
|
|
- |
|
|
|
|
331,331 |
|
|
|
|
|
|
|
Stockholders' equity (deficiency): |
|
|
|
|
|
Preferred stock, $0.0001 par value, 1,000,000 shares
authorized: |
|
|
|
|
|
Successor Series A preferred stock, 8,635 shares
designated, |
|
|
|
|
|
8,635 shares issued and outstanding as of December 31,
2022 |
|
|
1 |
|
|
|
|
- |
|
Successor Series B preferred stock, 5,062 shares
designated, |
|
|
|
|
|
5,062 shares issued and outstanding as of December 31,
2022 |
|
|
1 |
|
|
|
|
- |
|
Successor common stock, $0.0001 par value, 110,000,000 shares
authorized; |
|
|
|
|
9,016,139 shares issued and outstanding as of December 31,
2022 |
|
|
902 |
|
|
|
|
- |
|
Predecessor common stock, $0.00001 par value, 75,000,000 shares
authorized; |
|
|
|
|
24,167,257 shares issued and outstanding as of December 31,
2021 |
|
|
- |
|
|
|
|
242 |
|
Additional paid-in-capital |
|
|
104,583,271 |
|
|
|
|
40,065,109 |
|
Accumulated deficit |
|
|
(4,921,178 |
) |
|
|
|
(52,896,817 |
) |
Total stockholders' equity (deficiency) |
|
|
99,662,997 |
|
|
|
|
(12,831,466 |
) |
|
|
|
|
|
|
Total liabilities, temporary equity and stockholders' equity
(deficiency) |
$ |
118,506,271 |
|
|
|
$ |
1,126,174 |
|
|
|
|
|
|
|
|
ZYVERSA
THERAPEUTICS, INC. |
CONDENSED
CONSOLIDATED STATEMENTS OF OPERATIONS |
|
|
|
|
|
|
|
|
|
Successor |
|
|
Predecessor |
|
For the
period |
|
|
For the
period |
|
For the
year |
|
December
13 |
|
|
January
1 |
|
ended |
|
through |
|
|
through |
|
|
|
December
31, |
|
|
December
12, |
|
December
31, |
|
2022 |
|
|
2022 |
|
2021 |
Operating Expenses: |
|
|
|
|
|
|
Research and development |
$ |
399,894 |
|
|
|
$ |
5,407,859 |
|
|
$ |
2,124,277 |
|
General and administrative |
|
420,174 |
|
|
|
|
7,605,205 |
|
|
|
5,580,099 |
|
Total operating expenses |
|
820,068 |
|
|
|
|
13,013,064 |
|
|
|
7,704,376 |
|
Loss from operations |
|
(820,068 |
) |
|
|
|
(13,013,064 |
) |
|
|
(7,704,376 |
) |
Other (income) expense: |
|
|
|
|
|
|
Interest expense |
|
- |
|
|
|
|
427,542 |
|
|
|
821,366 |
|
Change in fair value of derivative liabilities |
|
- |
|
|
|
|
607,001 |
|
|
|
(228,100 |
) |
Gain on forgiveness of PPP Loan |
|
- |
|
|
|
|
- |
|
|
|
(213,481 |
) |
Pre-Tax Net Loss |
|
(820,068 |
) |
|
|
|
(14,047,607 |
) |
|
|
(8,084,161 |
) |
Income tax benefit |
|
745,050 |
|
|
|
|
- |
|
|
|
- |
|
Net loss |
|
(75,018 |
) |
|
|
|
(14,047,607 |
) |
|
|
(8,084,161 |
) |
Deemed dividend to preferred
stockholders |
|
- |
|
|
|
|
(10,015,837 |
) |
|
|
- |
|
Net loss attributable to common stockholders |
$ |
(75,018 |
) |
|
|
$ |
(24,063,444 |
) |
|
$ |
(8,084,161 |
) |
|
|
|
|
|
|
|
Net loss per share basic and diluted |
$ |
(0.01 |
) |
|
|
$ |
(0.99 |
) |
|
$ |
(0.33 |
) |
Weighted average common shares outstanding basic and diluted |
|
9,016,139 |
|
|
|
|
24,194,270 |
|
|
|
24,167,257 |
|
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