原始出處紀錄
Phase 2 期中數據顯示,76 名鉑類抗藥性/難治性卵巢癌患者中,ORR 達 46%,中位 DOR 為 10 個月。FDA 回饋支持 2027 年 Q1 提交 NDA 申請加速核准。卵巢癌群組主要分析及其他群組完整數據將於 2026 年 Q4 醫學會議發表。
EX-99.1 2 d441751dex991.htm EX-99.1 EX-99.1 Exhibit 99.1 PMV Pharmaceuticals Announces Updated Promising Rezatapopt Monotherapy Interim Ovarian Cancer Data From PYNNACLE Phase 2 Pivotal Trial • 46% ORR observed among 76 evaluable patients in the ovarian cancer cohort with a median duration of response of 10.0 months • Recent FDA interaction supports NDA submission strategy for accelerated approval of rezatapopt for platinum-resistant/refractory ovarian cancer, with submission planned in first quarter of 2027 • PMV plans to provide an update on all PYNNACLE Phase 2 pivotal trial cohorts at a medical conference in fourth quarter of 2026 PRINCETON, N.J. , August 31, 2026 (GLOBE NEWSWIRE) — PMV Pharmaceuticals, Inc. (“PMV Pharma” or the “Company”; Nasdaq: PMVP), a precision oncology