Press Release: PMV Pharmaceuticals Reports Full Year 2025 Financial Results and Corporate Highlights

Dow Jones03-06
   -- Enrollment remains on track in Phase 2 pivotal portion of PYNNACLE trial 
      evaluating rezatapopt as monotherapy in platinum-resistant/refractory 
      ovarian cancer patients with a TP53 Y220C mutation 
 
   -- Rezatapopt granted Orphan Drug Designation by the U.S. Food and Drug 
      Administration for the treatment of TP53 Y220C positive ovarian cancer 
 
   -- New England Journal of Medicine published first-in-human rezatapopt data 
      showing selective reactivation of mutant p53 in advanced solid tumors 
 
   -- Rezatapopt New Drug Application submission for 
      platinum-resistant/refractory ovarian cancer planned in first quarter of 
      2027 
 
   -- Cash, cash equivalents, and marketable securities of $112.9 million as of 
      December 31, 2025 providing expected cash runway to end of second quarter 
      of 2027 

PRINCETON, N.J., March 06, 2026 (GLOBE NEWSWIRE) -- PMV Pharmaceuticals, Inc. ("PMV Pharma" or the "Company"; Nasdaq: PMVP), a precision oncology company pioneering the discovery and development of small molecule therapies targeting p53, today reported financial results for the full year ended December 31, 2025, and provided a corporate update.

"2025 was an important and productive year for PMV Pharma as we reported positive Phase 2 interim data from the registrational PYNNACLE clinical trial and made significant progress in enrolling the study," said David Mack, Ph.D., President and Chief Executive Officer of PMV Pharma. "We look forward to submitting an NDA in the first quarter of 2027 for rezatapopt in platinum-resistant/refractory ovarian cancer."

PYNNACLE Phase 2 Monotherapy Update:

   -- Enrollment is on track in the Phase 2 monotherapy portion of the PYNNACLE 
      clinical trial. The multicenter, single-arm, registrational Phase 2 study 
      is assessing rezatapopt as monotherapy at a dose of 2000 mg once-daily in 
      patients with TP53 Y220C advanced solid tumors. 
 
   -- PMV Pharma anticipates submitting a New Drug Application (NDA) for 
      rezatapopt in platinum-resistant/refractory ovarian cancer patients with 
      a TP53 Y220C mutation in the first quarter of 2027. 

Full Year 2025 and Recent Corporate Highlights:

   -- On March 2, 2026, the U.S. Food and Drug Administration (FDA) granted 
      Orphan Drug Designation $(ODD)$ to rezatapopt for the treatment of TP53 
      Y220C positive ovarian cancer, fallopian tube cancer, and primary 
      peritoneal cancer. The FDA provides ODD status to drugs intended for the 
      safe and effective treatment, diagnosis, or prevention of rare diseases 
      that affect fewer than 200,000 people in the U.S. Benefits of the 
      designation may include exemption from certain FDA fees, financial 
      incentives for qualified clinical development, and seven years of market 
      exclusivity in the U.S. if the treatment is approved. 
 
   -- Phase 1 results from the ongoing Phase 1/2 PYNNACLE study were published 
      in the New England Journal of Medicine, "Phase 1 Study of Rezatapopt, a 
      p53 Reactivator, in TP53 Y220C-Mutated Tumors." The manuscript 
      highlighted that rezatapopt demonstrated antitumor activity in heavily 
      pretreated patients across multiple solid tumor types which provided 
      proof-of-concept for p53 reactivation. Clinical activity and biomarker 
      data were consistent with selective binding to the Y220C pocket and 
      restoration of wild-type p53 tumor suppressor function. 
 
   -- Updated data from the ongoing PYNNACLE Phase 2 trial were presented as an 
      oral presentation at the 2025 AACR-NCI-EORTC International Conference on 
      Molecular Targets and Cancer Therapeutics based on a September 4, 2025 
      data cut-off. 
 
          -- 34% overall response rate $(ORR)$ observed among 103 evaluable 
             patients across all cohorts with a median duration of response of 
             7.6 months. 
 
          -- 46% ORR observed among 48 evaluable patients in ovarian cancer 
             cohort with a median duration of response of 8.0 months. 
 
          -- Treatment-related adverse events (TRAEs) were mostly Grade 1-2 
             with the most frequent TRAEs observed (>15%) being nausea, fatigue, 
             blood creatinine increased, and alanine aminotransferase $(ALT)$ 
             increased. 
 
   -- Natural history study results were also presented at the 2025 
      AACR-NCI-EORTC International Conference on Molecular Targets and Cancer 
      Therapeutics where TP53 Y220C--mutant advanced solid tumors were 
      associated with poor outcomes reinforcing the significant unmet medical 
      need addressed by rezatapopt. 
 
   -- New findings from the rezatapopt PYNNACLE Phase 2 trial in ovarian cancer 
      were presented at the 2026 European Society of Gynecologic Oncology 
      Congress, demonstrating robust and consistent ORRs across key ovarian 
      cancer subgroups. 
 
          -- The ORR subgroup data included those with platinum-resistant, 
             platinum-refractory disease, prior systemic therapies and folate 
             receptor alpha status, that provide further evidence of the broad 
             efficacy of rezatapopt within ovarian cancer patients. 
 
          -- After the September 4, 2025 data cut-off, among the 48 evaluable 
             patients in the ovarian cancer cohort, a 50% ORR was observed with 
             23 confirmed responses and one unconfirmed partial response. 

Fiscal Year 2025 Financial Results

   -- As of December 31, 2025, PMV Pharma had $112.9 million in cash, cash 
      equivalents, and marketable securities, compared to $183.3 million at 
      December 31, 2024. Net cash used in operations was $73.6 million for the 
      year ended December 31, 2025, compared to $51.3 million for the year 
      ended December 31, 2024. 
 
   -- Net loss for the year ended December 31, 2025, was $77.7 million compared 
      to $58.7 million for the year ended December 31, 2024. 
 
   -- Research and development (R&D) expenses were $69.9 million for the year 
      ended December 31, 2025, compared to $58.5 million for the year ended 
      December 31, 2024. The increase in R&D expenses was primarily related to 
      clinical expenses for advancing rezatapopt, the Company's lead product 
      candidate. 
 
   -- General and administrative (G&A) expenses were $16.3 million for the year 
      ended December 31, 2025, compared to $26.9 million for the year ended 
      December 31, 2024. The decrease in G&A expenses was primarily due to 
      lower facility-related and personnel costs following the relocation of 
      the Company's lab and office space and staff reductions in the prior 
      year. 

About Rezatapopt

Rezatapopt (PC14586) is a first-in-class, small molecule, p53 reactivator designed to selectively bind to the pocket in the p53 Y220C mutant protein, restoring the wild-type tumor-suppressor function. The U.S. Food and Drug Administration granted Fast Track designation to rezatapopt for the treatment of patients with locally advanced or metastatic solid tumors with a p53 Y220C mutation and Orphan Drug Designation for the treatment of TP53 Y220C positive ovarian cancer, fallopian tube cancer, and primary peritoneal cancer.

About the PYNNACLE Clinical Trial

The ongoing Phase 1/2 PYNNACLE clinical trial is evaluating rezatapopt in patients with advanced solid tumors harboring a TP53 Y220C mutation. The primary objective of the Phase 1 portion of the clinical trial was to determine the maximum tolerated dose and recommended Phase 2 dose (RP2D) of rezatapopt when administered orally to patients. Safety, tolerability, pharmacokinetics and effects on biomarkers were also assessed. The Phase 2 portion is a registrational, single arm, expansion basket clinical trial comprising five cohorts (ovarian, lung, breast, and endometrial cancers, and other solid tumors) with the primary objective of evaluating the efficacy of rezatapopt at the RP2D in patients with TP53 Y220C and KRAS wild-type advanced solid tumors, conducted across approximately 70 sites.

For more information about the Phase 1/2 PYNNACLE clinical trial, refer to www.clinicaltrials.gov (NCT trial identifier NCT04585750).

About PMV Pharma

PMV Pharma is a precision oncology company pioneering the discovery and development of small molecule therapies targeting p53. TP53 mutations are found in approximately half of all cancers. Our co-founder, Dr. Arnold Levine, established the field of p53 biology when he discovered the p53 protein in 1979. Bringing together leaders in the field to utilize more than four decades of p53 biology, PMV Pharma combines unique biological understanding with a pharmaceutical development focus. PMV Pharma is headquartered in Princeton, New Jersey. For more information, please visit www.pmvpharma.com.

Forward-Looking Statements

Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, statements regarding the Company's future plans or expectations for rezatapopt, including our ability to obtain approval as a treatment option as a monotherapy, expectations regarding timing, enrollment status and success of the Phase 2 portion of the current clinical trial for rezatapopt and filing of an New Drug Application (NDA) for platinum-resistant/refractory ovarian cancer, the benefits of FDA's grant of Orphan Drug Designation (ODD) for rezatapopt, and the timing and expectations with respect to our projected cash runway. Any forward-looking statements in this statement are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in

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