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PMV Pharmaceuticals reported its Q4 and full year 2020 financial results, highlighting the initiation of Phase 1/2 study of PC14586 and a strengthened financial position with $361.4 million in cash, cash equivalents, and marketable securities.
Initiated Phase 1/2 study of PC14586 in patients with advanced solid tumors that have a p53 Y220C mutation.
PC14586 granted Fast Track designation by the U.S. FDA.
Deepika Jalota, Pharm. D. was appointed to Chief Regulatory and Quality Officer.
Scientific Advisory Board was expanded with appointment of Guillermina (Gigi) Lozano, Ph.D.
The company did not provide specific forward guidance in this report.