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Genentech: FDA Grants Priority Review To Fenebrutinib NDA For Relapsing And Primary Progressive MS
Source: Nasdaq
Healthcare & BiotechRegulation & LegislationProduct Launches
Genentech, a Roche affiliate, said the FDA accepted its New Drug Application for fenebrutinib under priority review. The application covers both relapsing and primary progressive disease indications, signaling an accelerated regulatory timeline for the therapy.
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