Forma Therapeutics Reports First Quarter 2022 Financial Results and Provides Business Update
Forma Therapeutics (NASDAQ: FMTX) announced its first quarter 2022 financial results, reporting a net loss of $44.1 million and a cash position of $441.3 million, expected to sustain operations through Q3 2024. Key updates include advancements in clinical trials for etavopivat and FT-7051 and the appointment of new leadership, enhancing its commitment to patient care. Upcoming milestones include pivotal trials for sickle cell disease and prostate cancer therapies, though potential COVID-19 impacts on enrollment remain a concern.
- Cash position of $441.3 million provides a runway through Q3 2024.
- Ongoing progress in clinical trials for etavopivat and FT-7051.
- Appointment of experienced leaders to improve patient care and research.
- Net loss increased to $44.1 million in Q1 2022 compared to $36.0 million in Q1 2021.
- R&D expenses rose to $31.3 million, up from $26.3 million year-over-year.
- Ongoing COVID-19 pandemic may impact clinical trial enrollments.
Clinical programs advancing in rare hematologic diseases and cancers
Cash balance of
“The first quarter of 2022 was one of continued progress in enrolling ongoing trials of etavopivat and FT-7051, and also expansion into other areas where red blood cell health may play an important role,” said
Key Business Updates
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Ifeyinwa (Ify) Osunkwo , M.D., MPH, joined Forma as the company’s inaugural chief patient officer and senior vice president.Dr. Osunkwo leads Forma’s efforts to be a trusted partner, collaborating with patients, advocates and healthcare providers who share a dedication to changing the care and treatment paradigm. -
Arturo Molina , M.D., elected to Board of Directors and R&D Committee.Dr. Molina is an internationally acclaimed clinician, hematology and oncology researcher, practicing physician and pioneer addressing healthcare inequities. He has over 25 years of experience in biopharma, hematology and oncology and currently serves as chief medical officer at Sutro Biopharma, Inc., where he is responsible for the clinical development of oncology and hematology therapeutics. -
Virtual Research and Development (R&D) Day to be heldMay 26, 2022 . The company will provide an overview of its clinical development programs and research pipeline strategy, including the introduction of a new molecule currently undergoing investigational new drug application enabling studies. The live webcast will be available in the “News & Investors” section of Forma’s website.
Upcoming Milestones
- Patient enrollment in global pivotal Phase II/III trial of etavopivat for the treatment of SCD, the Hibiscus Study. The first interim analysis (IA1) in the Hibiscus Study is expected to be reached by the end of 2022. IA1 is designed to select the dose for the Phase III portion of the trial.
- Additional etavopivat development programs. Forma has initiated a Phase II trial in patients with either transfusion dependent SCD, transfusion dependent thalassemia, or non-transfusion dependent thalassemia, with initial results expected in late 2022. During 2022, Forma plans to begin clinical trials in pediatric SCD and lower-risk myelodysplastic syndrome (MDS).
- Update on FT-7051 clinical trial in mCRPC. Men with metastatic castration-resistant prostate cancer (mCRPC) continue to be enrolled in the Phase I trial. Forma plans to provide an update at its May R&D Day and further results later in 2022.
- Possibility of COVID-19 impact remains. The COVID-19 pandemic remains a factor in the successful completion of these milestones and ongoing clinical trials. Many clinical trials across the biopharma industry, including Forma’s, have been impacted by the COVID-19 pandemic. Clinical trial sites implementing new policies in response to COVID-19 have impacted enrollment of clinical trials and/or the ability to access sites participating in clinical trials.
Financial Results
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Cash Position: Cash, cash equivalents and marketable securities were
as of$441.3 million March 31, 2022 , as compared to as of$490.3 million December 31, 2021 . Current cash runway is projected through the third quarter of 2024. -
R&D Expenses: R&D expenses were
for the quarter ended$31.3 million March 31, 2022 , as compared to for the quarter ended$26.3 million March 31, 2021 . The increase was primarily attributable to an increase in research and development staff to support advancement of etavopivat and other programs, an increase in equity-based compensation, the conduct of our Phase II/III trial in SCD patients, and study start-up costs related to our Phase II trial of etavopivat in thalassemia patients. -
General and Administrative (G&A) Expenses: G&A expenses were
for the quarter ended$13.1 million March 31, 2022 , as compared to for the quarter ended$9.9 million March 31, 2021 . The increase was primarily attributable to equity-based compensation, costs due to executive and staff hiring, and other related general and administrative costs. -
Net Loss: Net loss was
for the quarter ended$44.1 million March 31, 2022 , as compared to net loss of for the quarter ended$36.0 million March 31, 2021 .
Forma will conduct a conference call and webcast
The live webcast will be available in the “News & Investors” section of Forma’s website www.FormaTherapeutics.com.
About
Forward-looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, express or implied statements regarding the company’s beliefs and expectations regarding its: business plans and objectives; future plans for etavopivat and FT-7051, including expectations regarding potential development expansion plans as well as the enrollment, timing, success and data announcements of planned and ongoing clinical trials; therapeutic potential, clinical benefits, mechanisms of action and safety of our product candidates; upcoming milestones and planned additional trials for the company’s product candidates; growth as a company; upcoming presentations of our R&D programs, including the introduction of a new molecule and related studies; uses and need of capital, expenses and other financial results currently or in the future; and the potential impact of COVID-19 on patient retention and enrollment, future operations or clinical trials. The words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.
Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, those risks and uncertainties associated with the following: the impact of the COVID-19 pandemic on the company’s business, operations, supply chain, patient enrollment and retention, clinical trials, strategy, goals and anticipated milestones, as well as global economies and financial markets; the therapeutic potential of our product candidates and the timing and completion of our clinical trials and related data analyses; positive results from a clinical study may not necessarily be predictive of the results of future or ongoing clinical studies; any one or more of our product candidates may not be successfully developed and commercialized; regulatory developments in
Selected Financial Information |
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(in thousands except share and per share data) |
||||||||
(unaudited) |
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Statement of Operations Items: |
For the Three Months Ended |
|||||||
| 2022 |
|
2021 |
|||||
Collaboration revenue | $ | — |
|
$ | — |
|
||
Operating expenses: | | | ||||||
Research and development | | 31,273 |
|
| 26,343 |
|
||
General and administrative | | 13,136 |
|
| 9,867 |
|
||
Total operating expenses | | 44,409 |
|
| 36,210 |
|
||
Loss from operations | | (44,409 |
) |
| (36,210 |
) |
||
Other income: | | | ||||||
Interest income | | 289 |
|
| 262 |
|
||
Other expense, net | | (35 |
) |
| (4 |
) |
||
Total other income, net | | 254 |
|
| 258 |
|
||
Loss before taxes | | (44,155 |
) |
| (35,952 |
) |
||
Income tax expense | | 3 |
|
| 8 |
|
||
Net loss and comprehensive loss | $ | (44,158 |
) |
$ | (35,960 |
) |
||
Net loss allocable to shares of common stock, basic and diluted | $ | (44,158 |
) |
$ | (35,960 |
) |
||
Net loss per share of common stock, basic and diluted | $ | (0.93 |
) |
$ | (0.76 |
) |
||
Weighted-average shares of common stock outstanding, basic and diluted | | 47,561,631 |
|
| 47,295,013 |
|
Selected Balance Sheet Items: | ||||||
| ||||||
Cash, cash equivalents, and marketable securities | $ | 441,343 |
$ | 490,273 |
||
Total assets | $ | 514,497 |
$ | 561,061 |
||
Accounts payable, accrued expenses, and other current liabilities | $ | 26,247 |
$ | 35,018 |
||
Total stockholders’ equity | $ | 461,193 |
$ | 498,356 |
View source version on businesswire.com: https://www.businesswire.com/news/home/20220506005072/en/
Media:
Porter Novelli
caitlin.hunt@porternovelli.com
Investors:
mcorso@formatherapeutics.com
Source:
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