via NewMediaWire -- Timber Pharmaceuticals, Inc.
("Timber" or the “Company”) (NYSE American: TMBR), a
biopharmaceutical company focused on the development and
commercialization of treatments for rare and orphan dermatologic
diseases, today provided a business update and announced financial
results for the first quarter of 2022, ended March 31, 2022.
John Koconis, Chairman and Chief Executive Officer
of Timber, commented, “Timber’s lead asset, TMB-001, continues to
progress following the receipt of Fast Track designation late last
month, which is an important milestone on the path to approval. We
believe that TMB-001 has the potential to be the first FDA approved
therapy for Congenital Ichthyosis (CI), which has no FDA-approved
treatments and limited therapeutic options, and as such, we’ve
prioritized its development. This decision follows a series of
milestones that includes reporting positive top-line results from
our Phase 2b CONTROL study and the successful completion of an
end-of-Phase 2 meeting with the FDA. We also expect to
present the Phase 2b data at a number of medical conferences in the
U.S. and internationally over the next several months. Near term,
we remain focused on launching the Phase 3 ASCEND clinical trial by
June 30th, 2022 and advancing the development of this therapy to
the patient as quickly as possible.”
Recent Highlights
· Most
recently, and subsequent to quarter end, Timber announced that the
U.S. Food and Drug Administration (FDA) granted Fast Track
designation to its lead asset, TMB-001, a topical isotretinoin
formulated using Timber's patented IPEG™ delivery system, for the
treatment of X-linked recessive ichthyosis (XRI) and autosomal
recessive congenital ichthyosis lamellar ichthyosis
(ARCI-LI). Fast Track status facilitates the development
and expedites the review of drugs that treat serious conditions and
fill an unmet medical need.
· In
February 2022, Timber announced the successful completion of an
End-of-Phase 2 meeting with the U.S. Food and Drug Administration
(FDA) that resulted in a clear path to the launch of a pivotal
Phase 3 study for TMB-001. Timber plans to initiate the Phase 3
study by June 30th, 2022.
· In
March 2022, Christopher Bunick, MD, PhD, Yale University School of
Medicine, made a late-breaking presentation of a sub-analysis of
Timber’s Phase 2b CONTROL study data that evaluated TMB-001 at the
American Academy of Dermatology (AAD) 2022 Annual Meeting in
Boston, MA. The sub-analysis assessed whether primary
efficacy results for TMB-001 differed by CI subtype, and the
results demonstrated that patients could achieve treatment success
with TMB-001 regardless of the subtype of congenital ichthyosis
(CI).
· Timber
ended the first quarter with $13.9 million in cash and common
shares outstanding of 63.7 million on March 31, 2022.
· Timber
recognized revenue of $83,177 in the first quarter of 2022 compared
to $40,734 for the first quarter of 2021. Revenue for both periods
consisted of reimbursements from achieving certain clinical
milestones in the development of TMB-001, part of a $1.5 million
grant from the FDA’s Orphan Products Clinical Trials Grants
Program.
For Timber’s complete financial results for the
three-month period ended March 31, 2022, see the Company’s
Quarterly Form 10-Q filed with the Securities and Exchange
Commission on May 12, 2022.
About Timber Pharmaceuticals, Inc.
Timber Pharmaceuticals, Inc. is a
biopharmaceutical company focused on the development and
commercialization of treatments for rare and orphan dermatologic
diseases. The Company's investigational therapies have proven
mechanisms-of-action backed by decades of clinical experience and
well-established CMC (chemistry, manufacturing and control) and
safety profiles. The Company is initially focused on developing
non-systemic treatments for rare dermatologic diseases including
congenital ichthyosis (CI), facial angiofibromas (FAs) in tuberous
sclerosis complex (TSC), and other sclerotic skin diseases. For
more information, visit www.timberpharma.com.
Forward-Looking Statements
This press release 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 and regulatory timelines, market opportunity,
competitive position, intellectual property rights, possible or
assumed future results of operations, business strategies,
potential growth opportunities and other statements 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 Annual Report on
Form 10-K for the year ended December 31, 2021 as well as other
documents filed by the Company from time to time thereafter with
the Securities and Exchange Commission. 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.
For more information, contact:
Timber Pharmaceuticals, Inc.
John Koconis
Chairman and Chief Executive Officer
jkoconis@timberpharma.com
Investor Relations:
Stephanie Prince
PCG Advisory
(646) 863-6341
sprince@pcgadvisory.com
Media Relations:
Adam Daley
Berry & Company Public Relations
(212) 253-8881
adaley@berrypr.com
- Tables Follow -
Timber Pharmaceuticals, Inc. & Subsidiaries |
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Condensed Consolidated Balance Sheets |
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March 31, |
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December 31, |
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2022 |
|
2021 |
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(unaudited) |
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ASSETS |
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Current
assets |
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Cash |
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$ |
13,860,273 |
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$ |
16,808,539 |
Other current assets |
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|
211,227 |
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|
310,238 |
Total current assets |
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|
14,071,500 |
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|
17,118,777 |
Deposits |
|
|
127,534 |
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|
127,534 |
Property and equipment, net |
|
|
19,109 |
|
|
16,377 |
Right of use asset |
|
|
562,236 |
|
|
638,786 |
Total
assets |
|
$ |
14,780,379 |
|
$ |
17,901,474 |
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LIABILITIES
AND STOCKHOLDERS' EQUITY |
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Current
liabilities |
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Accounts payable |
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$ |
818,811 |
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$ |
953,349 |
Accrued expenses |
|
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633,296 |
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|
850,557 |
Lease liability, current portion |
|
|
346,580 |
|
|
332,817 |
Redeemable Series A preferred stock under redemption |
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2,109,600 |
|
|
2,055,348 |
Total current liabilities |
|
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3,908,287 |
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4,192,071 |
Note payable |
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— |
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|
37,772 |
Lease liability |
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|
241,507 |
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|
331,152 |
Other liabilities |
|
|
73,683 |
|
|
73,683 |
Total
liabilities |
|
|
4,223,477 |
|
|
4,634,678 |
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Commitments
and contingencies |
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Stockholders' equity |
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Common stock,
par value $0.001; 450,000,000 shares authorized; 63,678,836 shares
issued and outstanding as of March 31, 2022, and
63,619,140 shares issued and outstanding as of
December 31, 2021 |
|
|
64,216 |
|
|
63,619 |
Additional
paid-in capital |
|
|
42,450,622 |
|
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42,087,719 |
Accumulated
deficit |
|
|
(31,957,936) |
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|
(28,884,542) |
Total
stockholders' equity |
|
|
10,556,902 |
|
|
13,266,796 |
Total
liabilities and stockholders' equity |
|
$ |
14,780,379 |
|
$ |
17,901,474 |
|
|
|
|
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Timber Pharmaceuticals, Inc. & Subsidiaries |
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Condensed Consolidated Statement of Operations |
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(Unaudited) |
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Three months ended March 31, |
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2022 |
|
2021 |
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Grant
revenue |
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$ |
83,177 |
|
$ |
40,734 |
Milestone
revenue |
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— |
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— |
Total revenue |
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83,177 |
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|
40,734 |
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Operating
costs and expenses |
|
|
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Research and development |
|
|
1,518,959 |
|
|
849,518 |
Research and development - license acquired |
|
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— |
|
|
— |
Transaction costs |
|
|
— |
|
|
— |
Selling, general and administrative |
|
|
1,702,395 |
|
|
1,065,389 |
Total operating expenses |
|
|
3,221,354 |
|
|
1,914,907 |
Loss from
operations |
|
|
(3,138,177) |
|
|
(1,874,173) |
|
|
|
|
|
|
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Other income
(expense) |
|
|
|
|
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Interest expense |
|
|
(54,252) |
|
|
— |
Other income |
|
|
75,000 |
|
|
— |
Forgiveness of PPP loan |
|
|
37,772 |
|
|
— |
Gain (loss) on foreign currency exchange |
|
|
6,262 |
|
|
(87) |
Total other income (expense) |
|
|
64,783 |
|
|
(87) |
Loss before
provision for income taxes |
|
|
(3,073,394) |
|
|
(1,874,260) |
Provision for income taxes |
|
|
— |
|
|
— |
Loss before
provision for income taxes |
|
|
(3,073,394) |
|
|
(1,874,260) |
Provision for
income taxes |
|
|
— |
|
|
— |
Net
loss |
|
|
(3,073,394) |
|
|
(1,874,260) |
Accrued dividend on preferred stock units |
|
|
— |
|
|
— |
Cumulative dividends on Series A preferred stock |
|
|
— |
|
|
(35,887) |
Net loss
attributable to common stockholders |
|
$ |
(3,073,394) |
|
$ |
(1,910,147) |
|
|
|
|
|
|
|
Basic and
diluted net loss per share attributable to common
stockholders |
|
$ |
(0.05) |
|
$ |
(0.05) |
Basic and diluted weighted
average number of shares outstanding |
|
|
63,637,712 |
|
|
35,079,143 |
|
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