PMV Pharma reported its Q3 2023 financial results, featuring updated Phase 1 data from the PYNNACLE clinical trial, demonstrating efficacy and safety of PC14586. The company ended the quarter with $238.1 million in cash, cash equivalents, and marketable securities.
Updated Phase 1 PYNNACLE trial data showed responses across multiple tumor types with a median duration of response of seven months.
An overall response rate of 38% was observed at the recommended Phase 2 dose for TP53 Y220C and KRAS wild-type patients.
A registrational Phase 2 clinical trial is expected to start in Q1 2024.
Enrollment is ongoing in the combination arm of the PYNNACLE study with PC14586 and KEYTRUDA® (pembrolizumab).
PMV Pharma plans to initiate a registrational tumor-agnostic Phase 2 clinical trial in early 2024 and continues to enroll patients in the combination arm of PYNNACLE evaluating PC14586 with KEYTRUDA®.