1차 출처 기록
FDA는 ESR1 변이 ER+/HER2- 진행성 또는 전이성 유방암에 대한 단독요법으로 vepdegestrant의 NDA에 대해 2026년 6월 5일을 PDUFA 조치일로 지정했습니다. Arvinas와 Pfizer는 공동 상업화를 진행하는 대신 제3자에게 상업화 권리를 아웃라이선스하기로 합의했습니다.
EX-99.1 2 arvnstrategicupdaterelea.htm EX-99.1 arvnstrategicupdaterelea Exhibit 99.1 Arvinas Provides Update on Collaboration with Pfizer and Announces Further Actions to Support Value Creation Arvinas and Pfizer plan to jointly select third party for the out-licensing and commercialization of vepdegestrant Additional cost optimization measures expected to realize total annual savings of more than $100 million compared to FY 2024 Board authorizes stock repurchase program of up to $100 million Reaffirms cash runway guidance through the second half of 2028 NEW HAVEN, Conn., Sept. 17, 2025 – Arvinas, Inc. (Nasdaq: ARVN) today provided an update on its collaboration with Pfizer Inc. (NYSE: PFE) for the co-development of vepdegestrant, an investigational oral PROTAC (PROteolysis TArgeting Chi