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Press release content from Globe Newswire. The AP news staff was not involved in its creation.
PRESS RELEASE: Paid content from Globe Newswire
Press release content from Globe Newswire. The AP news staff was not involved in its creation.

Timber Pharmaceuticals Provides Business Update and Announces Third Quarter 2021 Financial Results

November 15, 2021 GMT

Positive Top Line Phase 2b Study Data for Lead Asset TMB-001 and Capital Raise of $17.25 Million Announced Subsequent to Quarter End 

BASKING RIDGE, NJ, Nov. 15, 2021 (GLOBE NEWSWIRE) -- 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 ended September 30, 2021.

John Koconis, Chairman and Chief Executive Officer of Timber, commented, “In the third quarter Timber was excited to complete the Phase 2b CONTROL Study of congenital ichthyosis for its lead asset, TMB-001. The positive topline data was released in early October and demonstrated clinically meaningful efficacy with a favorable safety profile that supports continued development. We believe this data readout helped us to raise gross proceeds of $17.25 million of new capital, positioning Timber to proceed on its path toward a Phase 3 study. The new capital will also be used to complete the Phase 2b clinical trial evaluating TMB-002 (topical rapamycin) which recently completed enrolment, of which the top line data readout is expected in the third quarter of 2022. With new capital in place, we look forward to continuing to advance toward meeting the needs of patients with rare and orphan dermatologic diseases.”

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Recent Highlights

  • Timber completed the Phase 2b CONTROL Study of congenital ichthyosis (CI) for its lead asset, TMB-001, during the third quarter and announced top line results subsequent to quarter end. TMB-001 is a topical isotretinoin formulated using Timber’s patented IPEG™ delivery system for patients with moderate to severe CI. Clinically meaningful efficacy with a favorable safety profile demonstrated the potential of TMB-001 to be an important option for the treatment of CI where no FDA-approved treatments are currently available and the standard of care is limited. Timber is planning for an end-of-Phase 2 meeting with the FDA in the beginning of 2022 and intends to begin the Phase 3 study of TMB-001 in the second quarter of 2022. 

  • Recruitment was completed for the ongoing Phase 2b clinical trial evaluating TMB-002 for the treatment of facial angiofibromas (FAs) in tuberous sclerosis complex (TSC), near the end of the third quarter of 2021. Data is expected six months from the date that the last patient was enrolled, as per protocol.

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  • Timber ended the third quarter with $3.4 million in cash and common shares outstanding of 36.7 million at September 30, 2021, prior to the capital raise of gross proceeds of $17.25 million (inclusive of the over-allotment option) that closed in early November 2021, in which 26,953,125 shares and 26,953,125 warrants were issued.

  • Timber recognized revenue of $266,974 in the third quarter of 2021, consisting of reimbursements as a result of achieving certain clinical milestones in the development of TMB-001, partof a $1.5 million grant from the FDA’s Orphan Products Clinical Trials Grants Program and from a TMB-002 milestone for a licensing agreement with AFT.

For Timber’s complete financial results for the period ended September 30, 2021, see the Company’s quarterly Form 10-Q filed with the Securities and Exchange Commission on November 15, 2021.

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, 2020 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:
Jenna Urban
Berry & Company Public Relations
(212) 253-8881
jurban@berrypr.com

- Tables Follow -

Timber Pharmaceuticals, Inc. & Subsidiaries
Condensed Consolidated Balance Sheets

      
30-Sep-21 31-Dec-20
 (unaudited)      
           
$ 3,357,136  $ 10,348,693 
  338,200    377,290 
  3,695,336    10,725,983 
  127,534    114,534 
  17,012    — 
  712,902    787,432 
$ 4,552,784  $ 11,627,949 
           
           
           
$ 1,042,290  $ 395,049 
  659,865    768,661 
  313,996    217,651 
  2,016,151    1,381,361 
  37,772    37,772 
  419,683    579,455 
  37,842    37,842 
  73,683    73,683 
  2,585,131    2,110,113 
           
           
           
  2,018,663    1,909,805 
           
           
  36,660    27,132 
  26,003,593    25,826,295 
  (26,091,263)   (18,245,396)
  (51,010)   7,608,031 
$ 4,552,784  $ 11,627,949 

Timber Pharmaceuticals, Inc. & Subsidiaries
Condensed Consolidated Statements of Operations
(Unaudited)

     Three Months Ended September 30    Nine Months Ended September 30
   2021  2020  2021  2020
                     
             
Grant revenue $ 225,128  $ 324,521  $ 400,789  $ 351,428 
Milestone revenue   41,846    —    295,738    — 
Total revenue   266,974    324,521    696,527    351,428 
                         
Operating costs and expenses                        
Research and development   1,974,193    685,207    4,623,811    2,239,607 
Research and development - license acquired   —    —    —    12,371,332 
Transaction costs   —    —    —    1,501,133 
Selling, general and administrative   1,296,641    1,233,849    3,918,042    2,745,728 
Total operating expenses   3,270,834    1,919,056    8,541,853    18,857,800 
Loss from operations   (3,003,860)   (1,594,535)   (7,845,326)   (18,506,372)
                         
Other (expense) income                        
Interest expense   —    —    —    (4,416,746)
Interest income   —    —    —    816,655 
Change in fair value of investment in BioPharmX   —    —    —    559,805 
Change in fair value of warrant liability   —    4,423,833    —    5,607,293 
Gain on foreign currency exchange   (1,544)   7,197    (541)   11,651 
Total other (expense) income   (1,544)   4,431,030    (541)   2,578,658 
Net (loss) income   (3,005,404)   2,836,495    (7,845,867)   (15,927,714)
Accrued dividend on preferred stock units   —    —    —    (52,669)
Cumulative dividends on Series A preferred stock   (36,685)   (36,685)   (108,858)   (53,831)
Net (loss) income attributable to common stockholders $ (3,042,089) $ 2,799,810  $ (7,954,725) $ (16,034,214)
             
Basic net (loss) income per share attributable to common stockholders $ (0.08) $ 0.15  $ (0.22) $ (1.32)
Diluted net (loss) income per share attributable to common stockholders $ (0.08) $ 0.14  $ (0.22) $ (1.32)
             
Basic weighted average number of shares outstanding   36,659,685    18,891,206    35,873,780    12,160,048 
Diluted weighted average number of shares outstanding   36,659,685    19,357,370    35,873,780    12,160,048