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Sage Therapeutics and Biogen Announce that the Phase 3 SKYLARK Study of Zuranolone in Postpartum Depression Met its Primary and All Key Secondary Endpoints
The primary endpoint was the change from baseline in the 17-item Hamilton Rating Scale for Depression HAMD-17 total score at Day 15.
About the SKYLARK Study The SKYLARK Study 217-PPD-301 was a Phase 3, randomized, double-blind, placebo-controlled trial assessing the efficacy and safety of zuranolone 50 mg compared to placebo in adult women with severe PPD.
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Sage Therapeutics to host conference call today at 8:00 am ET CAMBRIDGE, Mass.
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