Biotek-snakken — Maj 2026
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Arvinas Announces FDA Approval of VEPPANU (vepdegestrant) for the Treatment of ESR1m, ER+/HER2- Advanced Breast Cancer
– VEPPANU™ is the first-and-only FDA-approved PROTAC, a type of heterobifunctional protein degrader – – Approval received in advance of FDA-assigned PDUFA date of June 5, 2026; Arvinas and Pfizer remain on track to announce selection of a third party – – VEPPANU offers a new therapeutic option in ER+/HER2-, ESR1-mutated advanced or metastatic breast cancer, where treatment resistance remains a major clinical challenge – NEW HAVEN, Conn., May 01, 2026 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: AR
Yahoo Finance (finance.yahoo.com)
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Regnskab fra Arvinas 5 maj så vidt jeg husker, så må vi se hvad de siger om partneraftale forhandlingerne. De har hele tiden sagt at de skred godt fremad, men nu kom godkendelsen en god måned før tid, så håber de lukker aftalen meget snart. Ellers må Pfizer i sving!
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FDA godkender Pfizers og Arvinas’ brystkræftmiddel trods svage forsøgsdata
Pfizers milliardaftale, skuffende fase 3-resultater og fyringer hos Arvinas danner bagtæppe for godkendelsen af Veppanu.
(medwatch.dk)
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Pfizer, Arvinas join SERD club with Veppanu approval
Arvinas and Pfizer's Veppanu is the first PROTAC – and third oral SERD for breast cancer – to be approved by the FDA.
pharmaphorum (pharmaphorum.com)
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Arvinas to Report First Quarter 2026 Financial Results on May 12, 2026
NEW HAVEN, Conn., May 05, 2026 (GLOBE NEWSWIRE) -- Arvinas, Inc. (Nasdaq: ARVN), a biotechnology company working to create a new class of drugs based on targeted protein degradation, today announced that management will review first quarter 2026 financial results and provide a corporate update during a live webcast on Tuesday, May 12, 2026 at 8:00 a.m. ET. The webcast can be accessed under “Events and Presentations” on the investor page of the Arvinas website. A replay of the webcast will be ava
Yahoo Finance (finance.yahoo.com)
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Rigel Enters Exclusive Global Licensing Agreement for VEPPANU™ (vepdegestrant), an oral PROTAC, for the Treatment of 2L+ ER+/HER2-, ESR1m Advanced or Metastatic Breast Cancer
Rigel Pharmaceuticals, Inc. (Nasdaq: RIGL), a commercial stage biotechnology company focused on hematologic disorders and cancer, today announced that it has entered into an exclusive, global license agreement with Arvinas, Inc. (Arvinas) and Pfizer Inc. (Pfizer), subject to regulatory clearance, to develop, manufacture and commercialize VEPPANU™ (vepdegestrant), the first and only U.S. Food and Drug Administration (FDA)-approved oral PROteolysis TArgeting Chimera (PROTAC). PROTACs are part of a
Yahoo Finance (finance.yahoo.com)
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