BOSTON / Nov 06, 2024 / Business Wire / Verastem Oncology (Nasdaq: VSTM), a biopharmaceutical company committed to advancing new medicines for patients with cancer, today announced business updates and reported financial results for the third quarter ended September 30, 2024.
“In the third quarter of 2024, we made advancements in our recurrent low-grade serous ovarian cancer program, including sharing updated Phase 2 RAMP 201 data demonstrating robust and durable response rates, tumor reductions across a majority of patients regardless of their KRAS mutation status, and low discontinuation rates due to adverse events. We also completed our rolling NDA submission for recurrent KRAS mutant low-grade serous ovarian cancer and strengthened our balance sheet,” said Dan Paterson, president and chief executive officer of Verastem Oncology. “Looking ahead to the fourth quarter of 2024, we anticipate an FDA decision on the acceptance of our NDA, plan to submit our updated RAMP 201 trial data for publication and expect to prepare a U.S. IND application for VS-7375, an oral KRAS G12D (ON/OFF) inhibitor.”
Third Quarter 2024 and Recent Updates
Avutometinib and Defactinib Combination in Low-Grade Serous Ovarian Cancer (LGSOC)
Avutometinib in Combination with KRAS G12C Inhibitors in Non-Small Cell Lung Cancer (NSCLC)
Following a thorough evaluation of the Company’s lung cancer clinical development program, Verastem has decided to discontinue the Phase 1/2 RAMP 204 clinical trial evaluating the combination of avutometinib and adagrasib in patients with KRAS G12C-mutant NSCLC. There are no safety concerns with the RAMP 204 trial. The Company is prioritizing the Phase 1/2 RAMP 203 clinical trial, which is evaluating the doublet of avutometinib and sotorasib and the triplet combination of avutometinib and sotorasib plus defactinib in similar patient populations.
Avutometinib and Defactinib Combination in First-Line Metastatic Pancreatic Cancer
VS-7375/GFH375: Oral KRAS G12D (ON/OFF) Inhibitor
Third Quarter 2024 Financial Results
Verastem Oncology ended the third quarter of 2024 with cash, cash equivalents and short-term investments of $113.2 million which provides an expected cash runway through the potential approval of avutometinib and defactinib for recurrent LGSOC in mid-2025.
Total operating expenses for the three months ended September 30, 2024 (the “2024 Quarter”) were $37.0 million, compared to $21.3 million for the three months ended September 30, 2023 (the “2023 Quarter”).
Research & development expenses for the 2024 Quarter were $24.8 million, compared to $13.9 million for the 2023 Quarter. The increase of $10.9 million, or 78.4%, was primarily related to contract research organization costs, consulting costs, investigator fees associated with ensuring continued rapid start-up of RAMP 301, and a clinical milestone expense that was reached in the GenFleet G12D program.
Selling, general & administrative expenses for the 2024 Quarter were $12.3 million, compared to $7.4 million for the 2023 Quarter. The increase of $4.9 million, or 66.2%, was primarily related to a one-time cost associated with July 2024 financing activities, personnel costs, including non-cash stock compensation and additional costs in anticipation of a potential launch of avutometinib and defactinib in LGSOC.
Net loss for the 2024 Quarter was $24.0 million, or $0.60 per share (basic and diluted), compared to $20.0 million, or $0.75 per share (basic and diluted) for the 2023 Quarter.
For the 2024 Quarter, non-GAAP adjusted net loss was $35.3 million, or $0.88 per share (diluted) compared to non-GAAP adjusted net loss of $19.0 million, or $0.71 per share (diluted) for the 2023 Quarter. Please refer to the GAAP to non-GAAP Reconciliation attached to this press release.
Use of Non-GAAP Financial Measures
To supplement Verastem Oncology’s condensed consolidated financial statements, which are prepared and presented in accordance with generally accepted accounting principles in the United States (GAAP), the Company uses the following non-GAAP financial measures in this press release: non-GAAP adjusted net loss and non-GAAP net loss per share. These non-GAAP financial measures exclude certain amounts or expenses from the corresponding financial measures determined in accordance with GAAP. Management believes this non-GAAP information is useful for investors, taken in conjunction with the Company’s GAAP financial statements, because it provides greater transparency and period-over- period comparability with respect to the Company’s operating performance and can enhance investors’ ability to identify operating trends in the Company’s business. Management uses these measures, among other factors, to assess and analyze operational results and trends and to make financial and operational decisions. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of the Company’s operating results as reported under GAAP, not in isolation or as a substitute for, or superior to, financial information prepared and presented in accordance with GAAP. In addition, these non-GAAP financial measures are unlikely to be comparable with non-GAAP information provided by other companies. The determination of the amounts that are excluded from non-GAAP financial measures is a matter of management judgment and depends upon, among other factors, the nature of the underlying expense or income amounts. Reconciliations between these non-GAAP financial measures and the most comparable GAAP financial measures for the three and nine months ended September 30, 2024 and 2023 are included in the tables accompanying this press release after the unaudited condensed consolidated financial statements.
About the Avutometinib and Defactinib Combination
Avutometinib is a RAF/MEK clamp that induces inactive complexes of MEK with ARAF, BRAF and CRAF potentially creating a more complete and durable anti-tumor response through maximal RAS/MAPK pathway inhibition. In contrast to currently available MEK-only inhibitors, avutometinib blocks both MEK kinase activity and the ability of RAF to phosphorylate MEK. This unique mechanism allows avutometinib to block MEK signaling without the compensatory activation of MEK that appears to limit the efficacy of other MEK-only inhibitors.
Verastem Oncology is currently conducting clinical trials with avutometinib in RAS/MAPK driven tumors as part of its Raf And Mek Program or RAMP. Verastem is currently enrolling patients and activating sites for RAMP 301 (NCT06072781) an international Phase 3 confirmatory trial evaluating the combination of avutometinib and defactinib, a selective FAK inhibitor, versus standard chemotherapy or hormonal therapy for the treatment of recurrent low-grade serous ovarian cancer (LGSOC). RAMP 201 (NCT04625270) is a Phase 2 registration-directed trial of avutometinib in combination with defactinib in patients with recurrent LGSOC and enrollment has been completed for the RAMP 201 trial.
Verastem has completed its submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for the investigational combination of avutometinib and defactinib in adults with recurrent KRAS mutant LGSOC who received at least one prior systemic therapy in October 2024, with a potential FDA decision mid-2025. The FDA granted Breakthrough Therapy Designation of the investigational combination of avutometinib and defactinib for the treatment of patients with recurrent LGSOC after one or more prior lines of therapy, including platinum-based chemotherapy. Avutometinib alone or in combination with defactinib was also granted Orphan Drug Designation by the FDA for the treatment of LGSOC.
Verastem Oncology has established a clinical collaboration with Amgen to evaluate LUMAKRAS™ (sotorasib) in combination with avutometinib and defactinib in both treatment naive and in patients who progressed on a G12C inhibitor as part of the RAMP 203 trial (NCT05074810). Verastem has received Fast Track Designation from the FDA for the triplet combination in April 2024. RAMP 205 (NCT05669482), a Phase 1b/2 clinical trial evaluating avutometinib and defactinib with gemcitabine/nab-paclitaxel in patients with front-line metastatic pancreatic cancer, is supported by the PanCAN Therapeutic Accelerator Award. FDA granted Orphan Drug Designation to avutometinib and defactinib combination for the treatment of pancreatic cancer.
About VS-7375/GFH375
VS-7375/GFH375 is a potential best-in-class, potent and selective oral KRAS G12D (ON/OFF) inhibitor, identified as the lead discovery program from the Verastem Oncology discovery and development collaboration with GenFleet Therapeutics. GenFleet’s IND for VS-7375/GFH375 was approved in China in June 2024 and the Phase 1/2 trial in KRAS G12D-mutant solid tumors was subsequently initiated and the first patient was dosed in July 2024. The collaboration includes three discovery programs, the first being the KRAS G12D inhibitor, and provides Verastem Oncology with exclusive options to license three compounds selected for collaboration after successful completion of pre-determined milestones in Phase 1 trials. The licenses would give Verastem Oncology development and commercialization rights outside of the GenFleet territories of mainland China, Hong Kong, Macau, and Taiwan.
About Verastem Oncology
Verastem Oncology (Nasdaq: VSTM) is a late-stage development biopharmaceutical company committed to the development and commercialization of new medicines to improve the lives of patients diagnosed with cancer. Our pipeline is focused on RAS/MAPK-driven cancers, specifically novel small molecule drugs that inhibit critical signaling pathways in cancer that promote cancer cell survival and tumor growth, including RAF/MEK inhibition and FAK inhibition. For more information, please visit www.verastem.com and follow us on LinkedIn.
Forward-Looking Statements
This press release includes forward-looking statements about, among other things, Verastem Oncology’s programs and product candidates, strategy, future plans and prospects, including statements related to the expected timing for the FDA review of the rolling NDA submission for the avutometinib and defactinib combination in LGSOC, the structure of our planned and pending clinical trials, the potential clinical value of various of the Company’s clinical trials, including the RAMP 201, 205 and 301 trials, the timing of commencing and completing trials, including topline data reports, interactions with regulators, the timeline and indications for clinical development, regulatory submissions and the potential for and timing of commercialization of product candidates and potential for additional development programs involving Verastem Oncology’s lead compound, the expected outcome and benefits of our collaboration with GenFleet Therapeutics and the estimated addressable markets of our drug candidates. The words "anticipate," "believe," "estimate," "expect," "intend," "may," "plan," "predict," "project," "target," "potential," "will," "would," "could," "should," "continue," “can,” “promising” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.
Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties that could cause our actual results to differ materially from those expressed or implied in the forward-looking statements we make. Applicable risks and uncertainties include the risks and uncertainties, among other things, regarding: the success in the development and potential commercialization of our product candidates, including avutometinib in combination with other compounds, including defactinib, LUMAKRAS™ and others; the uncertainties inherent in research and development, such as negative or unexpected results of clinical trials, the occurrence or timing of applications for our product candidates that may be filed with regulatory authorities in any jurisdictions; whether and when regulatory authorities in any jurisdictions may approve any such applications that may be filed for our product candidates, and, if approved, whether our product candidates will be commercially successful in such jurisdictions; our ability to obtain, maintain and enforce patent and other intellectual property protection for our product candidates; the scope, timing, and outcome of any legal proceedings; decisions by regulatory authorities regarding trial design, labeling and other matters that could affect the timing, availability or commercial potential of our product candidates; whether preclinical testing of our product candidates and preliminary or interim data from clinical trials will be predictive of the results or success of ongoing or later clinical trials; that the timing, scope and rate of reimbursement for our product candidates is uncertain; that the market opportunities of our drug candidates are based on internal and third-party estimates which may prove to be incorrect; that third-party payors (including government agencies) may not reimburse; that there may be competitive developments affecting our product candidates; that data may not be available when expected; that enrollment of clinical trials may take longer than expected, which may delay our development programs, including delays in review by the FDA of our NDA submission in recurrent KRAS mutant LGSOC if enrollment in our confirmatory trial is not well underway at the time of submission, or that the FDA may require the Company to have completed enrollment or to enroll additional patients in the Company’s ongoing RAMP-301 confirmatory Phase 3 clinical trial prior to the FDA taking action on our NDA seeking accelerated approval; risks associated with preliminary and interim data, which may not be representative of more mature data, including with respect to interim duration of therapy data; that our product candidates will cause adverse safety events and/or unexpected concerns may arise from additional data or analysis, or result in unmanageable safety profiles as compared to their levels of efficacy; that we may be unable to successfully validate, develop and obtain regulatory approval for companion diagnostic tests for our product candidates that require or would commercially benefit from such tests, or experience significant delays in doing so; that the mature RAMP 201 data and associated discussions with the FDA may not support the scope of our NDA submission for the avutometinib and defactinib combination in LGSOC, including with respect to KRAS wild type LGSOC; that our product candidates may experience manufacturing or supply interruptions or failures; that any of our third party contract research organizations, contract manufacturing organizations, clinical sites, or contractors, among others, who we rely on fail to fully perform; that we face substantial competition, which may result in others developing or commercializing products before or more successfully than we do which could result in reduced market share or market potential for our product candidates; that we will be unable to successfully initiate or complete the clinical development and eventual commercialization of our product candidates; that the development and commercialization of our product candidates will take longer or cost more than planned, including as a result of conducting additional studies or our decisions regarding execution of such commercialization; that we may not have sufficient cash to fund our contemplated operations, including certain of our product development programs; that we may not attract and retain high quality personnel; that we or Chugai Pharmaceutical Co., Ltd. will fail to fully perform under the avutometinib license agreement; that the total addressable and target markets for our product candidates might be smaller than we are presently estimating; that we or Secura Bio, Inc. (Secura) will fail to fully perform under the asset purchase agreement with Secura, including in relation to milestone payments; that we will not see a return on investment on the payments we have and may continue to make pursuant to the collaboration and option agreement with GenFleet Therapeutics (Shanghai), Inc. (GenFleet), or that GenFleet will fail to fully perform under the agreement; that we may not be able to establish new or expand on existing collaborations or partnerships, including with respect to in-licensing of our product candidates, on favorable terms, or at all; that we may be unable to obtain adequate financing in the future through product licensing, co-promotional arrangements, public or private equity, debt financing or otherwise; that we will not pursue or submit regulatory filings for our product candidates; and that our product candidates will not receive regulatory approval, become commercially successful products, or result in new treatment options being offered to patients.
Other risks and uncertainties include those identified under the heading “Risk Factors” in the Company’s Annual Report on Form 10-K for the year ended December 31, 2023 as filed with the Securities and Exchange Commission (SEC) on March 14, 2024 and in any subsequent filings with the SEC, which are available at www.sec.gov. The forward-looking statements contained in this press release reflect Verastem Oncology’s views as of the date hereof, and the Company does not assume and specifically disclaims any obligation to update any forward-looking statements whether as a result of new information, future events or otherwise, except as required by law.
Verastem Oncology Condensed Consolidated Balance Sheets (in thousands) (unaudited) | ||||||
|
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| September 30, 2024 |
| December 31, 2023 | ||
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Cash, cash equivalents & short-term investments | $ | 113,175 |
| $ | 137,129 | |
Grant receivable |
| 200 |
|
| — | |
Prepaid expenses and other current assets |
| 7,287 |
|
| 6,553 | |
Property and equipment, net |
| 39 |
|
| 37 | |
Right-of-use asset, net |
| 625 |
|
| 1,171 | |
Restricted cash and other assets |
| 5,052 |
|
| 4,828 | |
Total assets | $ | 126,378 |
| $ | 149,718 | |
|
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|
| |||
Current Liabilities | $ | 37,374 |
| $ | 26,380 | |
Long term debt |
| 30,647 |
|
| 40,086 | |
Lease liability, long-term |
| — |
|
| 530 | |
Preferred stock tranche liability |
| — |
|
| 4,189 | |
Warrant liability |
| 26,138 |
|
| — | |
Convertible preferred stock |
| 21,159 |
|
| 21,159 | |
Stockholders’ equity |
| 11,060 |
|
| 57,374 | |
Total liabilities, convertible preferred stock and stockholders’ equity | $ | 126,378 |
| $ | 149,718 | |
Verastem Oncology Condensed Consolidated Statements of Operations (in thousands, except per share amounts) (unaudited) | ||||||||||||
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|
| Three months ended September 30, |
| Nine months ended September 30, | ||||||||
|
|
| 2024 |
|
| 2023 |
|
| 2024 |
|
| 2023 |
Revenue |
|
|
|
| ||||||||
Sale of COPIKTRA license and related assets | $ | — | $ | — | $ | 10,000 | $ | — | ||||
Total revenue |
| — |
| — |
| 10,000 |
| — | ||||
Operating expenses: |
|
|
|
| ||||||||
Research and development |
| 24,754 |
| 13,946 |
| 60,523 |
| 38,854 | ||||
Selling, general and administrative |
| 12,276 |
| 7,363 |
| 32,843 |
| 22,091 | ||||
Total operating expenses |
| 37,030 |
| 21,309 |
| 93,366 |
| 60,945 | ||||
Loss from operations |
| (37,030) |
| (21,309) |
| (83,366) |
| (60,945) | ||||
Other expense |
| (77) |
| (13) |
| (131) |
| (60) | ||||
Interest income |
| 831 |
| 2,247 |
| 3,181 |
| 4,345 | ||||
Interest expense |
| (1,148) |
| (1,129) |
| (3,416) |
| (3,019) | ||||
Change in fair value of preferred stock tranche liability |
| — |
| 200 |
| 4,189 |
| (320) | ||||
Change in fair value of warrant liability |
| 13,457 |
| — |
| 13,457 |
| — | ||||
Net loss | $ | (23,967) | $ | (20,004) | $ | (66,086) | $ | (59,999) | ||||
Net loss per share—basic and diluted | $ | (0.60) | $ | (0.75) | $ | (2.11) | $ | (2.93)(1) | ||||
Weighted average common shares outstanding used in computing: |
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| ||||||||
Net loss per share – basic and diluted |
| 40,258 |
| 26,790 |
| 31,350 |
| 20,452(1) | ||||
(1) Amounts have been retroactively restated to reflect the 1-for-12 reverse stock split effected on May 31, 2023 | ||||||||||||
Verastem Oncology Reconciliation of GAAP to Non-GAAP Financial Information (in thousands, except per share amounts) (unaudited) | ||||||||||||
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| Three months ended September 30, | Nine months ended September 30, | ||||||||||
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| 2024 |
| 2023 |
| 2024 |
| 2023 | ||||
Net loss reconciliation |
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Net loss (GAAP basis) | $ | (23,967) | $ | (20,004) | $ | (66,086) | $ | (59,999) | ||||
Adjust: |
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|
| ||||||||
Stock-based compensation expense |
| 1,935 |
| 1,517 |
| 35,323 |
| 4,262 | ||||
Non-cash interest, net |
| 201 |
| (371) |
| (212) |
| (295) | ||||
Change in fair value of preferred stock tranche liability |
| — |
| (200) |
| (4,189) |
| 320 | ||||
Change in fair value of warrant liability |
| (13,457) |
| — |
| (13,457) |
| — | ||||
Severance and Other |
| 10 |
| 47 |
| 619 |
| 85 | ||||
Adjusted net loss (non-GAAP basis) | $ | (35,278) | $ | (19,011) | $ | (78,002) | $ | (55,627) | ||||
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Reconciliation of net loss per share |
|
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Net loss per share – diluted (GAAP Basis) |
| (0.60) |
| (0.75) |
| (2.11) |
| (2.93)(1) | ||||
Adjust per diluted share: |
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| ||||||||
Stock-based compensation expense |
| 0.05 |
| 0.06 |
| 0.17 |
| 0.21(1) | ||||
Non-cash interest, net |
| — |
| (0.01) |
| (0.01) |
| (0.02)(1) | ||||
Change in fair value of preferred stock tranche liability |
| — |
| (0.01) |
| (0.13) |
| 0.02(1) | ||||
Change in fair value of warrant liability |
| (0.33) |
| — |
| (0.43) |
| — | ||||
Severance and Other |
| — |
| — |
| 0.02 |
| — | ||||
Adjusted net loss per share – diluted (non-GAAP basis) | $ | (0.88) | $ | (0.71) | $ | (2.49) | $ | (2.72)(1) | ||||
Weighted average common shares outstanding used in computing net loss per share—diluted |
| 40,258 |
| 26,790 |
| 31,350 |
| 20,452(1) | ||||
(1) Amounts have been retroactively restated to reflect the 1-for-12 reverse stock split effected on May 31, 2023 | ||||||||||||
| Last Trade: | US$3.95 |
| Daily Change: | 0.02 0.51 |
| Daily Volume: | 676,159 |
| Market Cap: | US$158.950M |
September 10, 2024 September 10, 2024 | |
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