Timber Pharmaceuticals Provides Business Update and Announces Third Quarter 2022 Financial Results
November 14 2022 - 7:00AM
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 third quarter of 2022, ended September 30, 2022.
John Koconis, Chairman and Chief Executive
Officer of Timber, commented, “In the third quarter, Timber
continued to progress and achieve important milestones. This
included receiving notice, and then the official orphan designation
in October, from the European Commission (EC) for TMB-001 for the
treatment of autosomal recessive congenital ichthyosis (ARCI). This
designation will provide Timber with market exclusivity for TMB-001
in the European Union once we receive FDA approval. Together with
the positive comments we received on our Pediatric Investigation
Plan (PIP), and the final discussion scheduled for mid-November, we
believe we have a path to filing a European Marketing Authorization
Application. These designations are in addition to the orphan
designation and associated market exclusivity for TMB-001 that
Timber was previously awarded in the U.S. Timber is
continuing to expand the intellectual property around our lead
program with an additional patent granted in the U.S. as well as
initial patents granted in S. Korea, Japan and Australia earlier in
2022.
“At TMB-001’s late stage of development, it’s
also appropriate for us to explore partnerships and licensing
agreements, and we’re speaking with many potential candidates
throughout Europe. During the quarter, we were excited to have the
Phase 2b results published in an online peer reviewed journal for
the first time, in the prestigious Journal of the American Academy
of Dermatology (JAAD). Recruitment for the pivotal Phase 3 ASCEND
clinical trial that we began in June is progressing on plan as
well. Timber ended the quarter with approximately $11.2 million in
cash, more than adequate runway to complete recruitment for the
approximately 140 patients required for the Phase 3 trial. We
recently effected a reverse stock split as we believe it is
important to maintain the listing of the Company’s common stock on
the NYSE American exchange. With this action, an improved capital
structure and TMB-001’s late stage of development, we believe that
Timber is better positioned to complete the development plan for
TMB-001,” concluded Mr. Koconis.
Recent Highlights
- Subsequent to quarter end, Timber received official
orphan designation from the European Commission (EC) for its lead
asset, TMB-001, a topical isotretinoin formulated using Timber's
patented IPEGTM delivery system, for the treatment of X-linked
recessive ichthyosis (XRI) and autosomal recessive congenital
ichthyosis lamellar ichthyosis (ARCI-LI).
- Also in late October, the European Medicines Agency (EMA)
Pediatric Committee (PDCO) provided positive comments on Timber’s
Pediatric Investigation Plan (PIP) for the treatment of ARCI and
X-linked recessive ichthyosis (XLRI), setting the basis for a final
discussion in mid-November, which is a prerequisite for filing a
Marketing Authorization Application (MAA) with the EMA. Timber
continued to expand its program by applying for European orphan
designation for TMB-001 for XLRI in late October.
- In September 2022, Timber announced that it had received
a positive opinion on its application for orphan designation from
the Committee for Orphan Medicinal Products (COMP) at the European
Medicines Agency (EMA) for TMB-001.
- In September 2022, Timber made multiple presentations at
the 31st Annual European Academy of Dermatology and Venereology
(EADV) Congress that highlighted the results of the Phase 2b
CONTROL Study. Timber expects additional publication of the Phase
2b study data analysis on TMB-001 in the coming months.
- In August 2022, the Journal of the American Academy
of Dermatology (JAAD) published online the results from the
Phase 2b CONTROL Study that demonstrated TMB-001s clinically
meaningful efficacy with a favorable safety profile. JAAD published
the TMB-001 Phase 2a data its November 2022 issue.
- On June 23, 2022, Timber announced that it had enrolled
the first patients in its Phase 3 ASCEND clinical trial.
Recruitment has been proceeding to plan with over 20% enrollment to
date. The pivotal trial is expected to enroll more than
140 patients with moderate to severe Congenital Ichthyosis at
leading research centers in the U.S., Canada, Italy, France,
and Germany. In Spring 2022, Timber received Breakthrough Therapy
designation and Fast Track designation from the U.S. Food and Drug
Administration (FDA) for TMB-001.
- Timber recognized no revenue in the third quarter of 2022
compared to revenue of $225,128 for the third quarter of 2021. For
the first nine months of 2022, Timber recognized revenue of $83,177
in the 2022 period and $400,789 in the 2021 period. Revenue for all
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.
- Timber ended the third quarter with approximately $11.2
million in cash and 2.7 million shares of common stock outstanding
after giving retroactive effect to a 1-for-50 reverse split of its
shares of common stock on November 9, 2022in order to regain
compliance with NYSE requirements. Subsequent to quarter end on
October 3, 2022, Timber raised $1.3 million in gross proceeds
through the sale of common stock and warrants.
For Timber’s complete financial results for the
three-month period ended September 30, 2022, see the Company’s
Quarterly Form 10-Q filed with the Securities and Exchange
Commission on November 14, 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), 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 ability to
regain compliance with the NYSE American’s continued listing
standards, 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 KoconisChairman
and Chief Executive Officerjkoconis@timberpharma.com
Investor Relations:Stephanie PrincePCG
Advisory(646) 863-6341sprince@pcgadvisory.com
Media Relations:Adam DaleyBerry & Company
Public Relations(212) 253-8881adaley@berrypr.com
- Tables Follow -
Timber
Pharmaceuticals, Inc. & Subsidiaries |
|
Condensed
Consolidated Balance Sheets |
|
|
|
|
|
|
|
|
|
|
September
30, |
|
December 31, |
|
|
|
2022 |
|
|
2021 |
|
|
|
|
|
(unaudited) |
|
|
|
|
ASSETS |
|
|
|
|
|
|
|
Current
assets |
|
|
|
|
|
|
|
Cash |
|
$ |
11,224,197 |
|
|
$ |
16,808,539 |
|
|
Prepaid research and development |
|
|
722,121 |
|
|
|
66,217 |
|
|
Other current assets |
|
|
296,038 |
|
|
|
244,021 |
|
|
Total current assets |
|
|
12,242,356 |
|
|
|
17,118,777 |
|
|
Deposits |
|
|
127,534 |
|
|
|
127,534 |
|
|
Property and equipment, net |
|
|
19,400 |
|
|
|
16,377 |
|
|
Right of use asset |
|
|
400,918 |
|
|
|
638,786 |
|
|
Total assets |
|
$ |
12,790,208 |
|
|
$ |
17,901,474 |
|
|
|
|
|
|
|
|
|
|
LIABILITIES AND STOCKHOLDERS' EQUITY |
|
|
|
|
|
|
|
Current
liabilities |
|
|
|
|
|
|
|
Accounts payable |
|
$ |
953,470 |
|
|
$ |
953,349 |
|
|
Accrued expenses |
|
|
1,960,065 |
|
|
|
850,557 |
|
|
Lease liability, current portion |
|
|
336,162 |
|
|
|
332,817 |
|
|
Short-term milestone payable due to Patagonia Pharmaceuticals
LLC |
|
|
1,750,000 |
|
|
|
— |
|
|
Redeemable Series A preferred stock under redemption (Notes
5 and 9) |
|
|
— |
|
|
|
2,055,348 |
|
|
Total current liabilities |
|
|
4,999,697 |
|
|
|
4,192,071 |
|
|
Note payable |
|
|
— |
|
|
|
37,772 |
|
|
Lease liability |
|
|
83,520 |
|
|
|
331,152 |
|
|
Other liabilities |
|
|
73,683 |
|
|
|
73,683 |
|
|
Total liabilities |
|
|
5,156,900 |
|
|
|
4,634,678 |
|
|
|
|
|
|
|
|
|
|
Commitments and contingencies (Note 7) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Stockholders' equity |
|
|
|
|
|
|
|
Preferred
stock - member units |
|
|
— |
|
|
|
— |
|
|
Common stock
- member units |
|
|
— |
|
|
|
— |
|
|
Common
stock, par value $0.001; 450,000,000 shares authorized; 2,670,856
shares issued and outstanding as of September 30, 2022, and
1,272,383 shares issued and outstanding as of
December 31, 2021 |
|
|
133,543 |
|
|
|
63,619 |
|
|
Additional
paid-in capital |
|
|
52,140,972 |
|
|
|
42,087,719 |
|
|
Accumulated
deficit |
|
|
(44,641,207 |
) |
|
|
(28,884,542 |
) |
|
Total
stockholders' equity |
|
|
7,633,308 |
|
|
|
13,266,796 |
|
|
Total liabilities and stockholders' equity |
|
$ |
12,790,208 |
|
|
$ |
17,901,474 |
|
|
|
|
|
|
|
|
|
|
Timber
Pharmaceuticals, Inc. & Subsidiaries |
|
|
Condensed
Consolidated Statement of Operations |
|
|
(Unaudited) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Three months ended September 30, |
|
Nine months ended September 30, |
|
|
|
|
|
2022 |
|
|
2021 |
|
|
2022 |
|
|
2021 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Grant
revenue |
|
$ |
— |
|
|
$ |
225,128 |
|
|
$ |
83,177 |
|
|
$ |
400,789 |
|
|
|
|
Milestone
revenue |
|
|
— |
|
|
|
41,846 |
|
|
|
— |
|
|
|
295,738 |
|
|
|
|
Total revenue |
|
|
— |
|
|
|
266,974 |
|
|
|
83,177 |
|
|
|
696,527 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating
costs and expenses |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Research and development |
|
|
1,790,528 |
|
|
|
1,974,193 |
|
|
|
7,200,987 |
|
|
|
4,623,811 |
|
|
|
|
Research and Development - Milestone expense for Patagonia
Pharmaceuticals LLC |
|
|
— |
|
|
|
— |
|
|
|
4,000,000 |
|
|
|
— |
|
|
|
|
Selling, general and administrative |
|
|
1,336,668 |
|
|
|
1,296,641 |
|
|
|
4,551,406 |
|
|
|
3,918,042 |
|
|
|
|
Total operating expenses |
|
|
3,127,196 |
|
|
|
3,270,834 |
|
|
|
15,752,393 |
|
|
|
8,541,853 |
|
|
|
|
Loss from
operations |
|
|
(3,127,196 |
) |
|
|
(3,003,860 |
) |
|
|
(15,669,216 |
) |
|
|
(7,845,326 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other income
(expense) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest expense |
|
|
(71,203 |
) |
|
|
— |
|
|
|
(167,531 |
) |
|
|
— |
|
|
|
|
Other income |
|
|
— |
|
|
|
— |
|
|
|
75,000 |
|
|
|
— |
|
|
|
|
Forgiveness of PPP loan |
|
|
— |
|
|
|
— |
|
|
|
37,772 |
|
|
|
— |
|
|
|
|
(Loss) gain on foreign currency exchange |
|
|
11,124 |
|
|
|
(1,544 |
) |
|
|
(32,690 |
) |
|
|
(541 |
) |
|
|
|
Provision for income taxes |
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
|
Loss
before provision for income taxes |
|
|
(3,187,275 |
) |
|
|
(3,005,404 |
) |
|
|
(15,756,665 |
) |
|
|
(7,845,867 |
) |
|
|
|
Provision for
income taxes |
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
|
Net
loss |
|
|
(3,187,275 |
) |
|
|
(3,005,404 |
) |
|
|
(15,756,665 |
) |
|
|
(7,845,867 |
) |
|
|
|
Accrued dividend on preferred stock units |
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
|
Dividends on Series A preferred stock |
|
|
— |
|
|
|
(36,685 |
) |
|
|
— |
|
|
|
(108,858 |
) |
|
|
|
Net
loss attributable to common stockholders |
|
$ |
(3,187,275 |
) |
|
$ |
(3,042,089 |
) |
|
$ |
(15,756,665 |
) |
|
$ |
(7,954,725 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic and diluted net loss per share attributable to common
stockholders |
|
$ |
(1.52 |
) |
|
$ |
(4.15 |
) |
|
$ |
(10.16 |
) |
|
$ |
(11.09 |
) |
|
|
|
Basic and diluted weighted average number of shares
outstanding |
|
|
2,095,091 |
|
|
|
733,194 |
|
|
|
1,550,326 |
|
|
|
717,476 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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