Timber Pharmaceuticals Provides Business Update and Announces Third Quarter 2021 Financial Results
Timber Pharmaceuticals, Inc. (NYSE American: TMBR) reported positive topline results from its Phase 2b CONTROL Study for lead asset TMB-001, showing meaningful efficacy and safety. Following this, the company raised $17.25 million in gross proceeds to fund further development, including a Phase 3 study planned for Q2 2022. Additionally, enrollment for the Phase 2b trial of TMB-002 has concluded, with data expected in Q3 2022. Timber ended Q3 2021 with $3.4 million in cash and reported revenue of $266,974, largely from clinical milestones.
- Positive topline results for TMB-001 from Phase 2b CONTROL Study
- Raised $17.25 million to support future studies
- Planning Phase 3 study for TMB-001 in Q2 2022
- Completed enrollment of Phase 2b trial for TMB-002, data expected Q3 2022
- None.
Positive Top Line Phase 2b Study Data for Lead Asset TMB-001 and Capital Raise of
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
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.
- 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 | ||||||||
FAQ
What were the key results from Timber's Phase 2b CONTROL Study for TMB-001?
How much capital did Timber raise in November 2021 and for what purpose?
When is Timber planning to begin the Phase 3 study for TMB-001?
What revenue did Timber report for Q3 2021?
When can we expect data from Timber's Phase 2b trial for TMB-002?
