已收盤 08-01 16:00:00 美东时间
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Arvinas, Inc. (Nasdaq: ARVN), a clinical-stage biotechnology company focused on targeted protein degradation, announced that its management will discuss the second-quarter 2025 financial results and provide a corporate update during a live webcast on August 6, 2025, at 8:00 a.m. ET. The webcast can be accessed via the company’s investor page, with a replay available post-event.
07-30 20:05
Celcuity shares jump as gedatolisib shows strong efficacy in HR+/HER2- breast cancer Phase 3 trial, with FDA filing expected in late 2025.
07-28 21:42
Arvinas (NASDAQ:ARVN) announced that president and CEO John Houston plans to retire from his roles at the biotech company following the appointment of a successor. The company has initiated a search f...
07-09 19:36
Arvinas, Inc. (NASDAQ:ARVN), a clinical-stage biotechnology company working to develop a new class of drugs based on targeted protein degradation, today announced that John Houston, Ph.D., Chairperson, Chief
07-09 19:05
John Houston, Ph.D., CEO and President of Arvinas, has announced his plans to retire upon the appointment of a new CEO. Houston will remain as Chairperson of Arvinas’ Board of Directors and the Board has initiated a search for his successor. Houston joined Arvinas in 2017 and has significantly advanced targeted protein degradation, successfully leading the company through pivotal milestones. The Board expresses gratitude for his leadership and is...
07-09 11:00
– ARV-393 demonstrated significant single-agent activity in models of nodal T-follicular helper cell lymphoma, angioimmunoblastic-type (also known as AITL) and transformed follicular lymphoma –– In combination with small
06-13 19:04
今日,Arvinas和辉瑞公司(PFE.US)宣布已为其联合开发的明星PROTAC分子vepdegestrant向美国FDA提交新药申请(NDA)。
06-09 21:21
Arvinas and Pfizer submitted an NDA to the FDA for vepdegestrant, a PROTAC ER degrader, to treat ESR1-mutated ER+/HER2- advanced or metastatic breast cancer. The application is supported by the Phase 3 VERITAC-2 trial, which demonstrated superior progression-free survival compared to fulvestrant. Results were presented at the 2025 ASCO Annual Meeting and published in the New England Journal of Medicine. Vepdegestrant has been granted Fast Track d...
06-06 11:00
– Company to showcase preclinical studies of ARV-393, an investigational oral PROTAC BCL6 degrader, as a single agent in models of nodal T-follicular helper cell lymphoma, angioimmunoblastic-type (AITL) and transformed
06-05 20:31