Endpoints News
GSK to license Hutchmed’s cancer drug Read in browser
Endpoints News
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3 September, 2026
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1. AbbVie claims Phase 3 win of multiple myeloma drug, seeking to enter crowded market
2. GSK to license Hutchmed’s dual-action cancer drug for $110M upfront
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Pfizer shares ADC rights with Medicus; RevMed updates lung cancer data
4. Take the Q3 Biopharma Sentiment Survey (BPSI)
5. Ultragenyx’s Angelman therapy fails Phase 3 trial in setback for company and patients
6. Summit, Akeso say ivonescimab clears OS bar in Phase 3 lung cancer trial
7. Superluminal secures $60M for Phase 1 of genetic obesity drug
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in focus
Drew Armstrong
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Two notes: 1) We're three weeks out from the Endpoints 11, our annual list of the most exciting startups in biotech. Join us on Sept. 24 in Boston for an evening of innovation, conversation and the unveiling of the new companies defining the future of medicine. 2) Our beloved people column, Peer Review, is on a break this week and won't publish tomorrow.

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Drew Armstrong
Executive Editor, Endpoints News
@ArmstrongDrew
1
by Lei Lei Wu

Ab­b­Vie said its T cell en­gager eten­tamig cut the risk of dis­ease pro­gres­sion or death by 60% com­pared with stan­dard ther­a­pies in a Phase 3...

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The China Biotech Debate: Washington, DC from POST-HOC
Secrecy, security and policy: round two of our China biotech series lands in Washington, with the policymakers who will decide the US posture toward its biggest rival. Seats are limited. Get your ticket now.
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by Elizabeth Cairns

GSK will spend $110 mil­lion up­front for a li­cense to a KRAS-EGFR an­ti­body con­ju­gate de­vel­oped by Hutchmed, with up to $1.185 bil­lion in biobucks on...

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News Briefing: Quick hits from the biopharma web
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by ENDPOINTS

Plus, news about No­var­tis.

🤝 Pfiz­er turns over ADC:The New York phar­ma is giv­ing Medicus Phar­ma co-de­vel­op­ment rights to a CD228-tar­get­ed an­ti­body-drug con­ju­gate known...

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