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FDA advisers pan Pfizer’s PARP drug; Sarepta to resume Duchenne study

Simon Osuji by Simon Osuji
May 23, 2025
in Technology
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Akeso claims another PD-1/VEGF win; FDA requests more data from Novavax
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An eight-member panel voted unanimously against wider use of Pfizer’s Talzenna in advanced prostate cancer. Elsewhere, U.K. regulators cleared Sarepta to restart an Elevidys study and Altos Labs bought a startup.

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