Sage Therapeutics, Inc. has a lot to figure out in the coming weeks, now that the US Food and Drug Administration has approved Zurzuvae (zuranolone) for postpartum depression (PPD) but rejected the drug for major depressive disorder (MDD). The company said that while it evaluates next steps for Zurzuvae in MDD based on the FDA’s complete response letter (CRL) for that indication, it will also put together a plan that reprioritizes its spending, including a “workforce reorganization.”
Cambridge, MA-based Sage and its partner Biogen, Inc
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