Sage’s oral postpartum depression drug ticks efficacy, safety boxes in key trial, easing fears of fainting risk

Pivotal data on Sage Therapeutics' {$SAGE} keenly-watched oral postpartum depression (PPD) drug showed that there was no loss of consciousness associated with the experimental treatment, unlike the drug developer's brexanolone — which must be administered via an infusion and is currently under FDA review. Late-stage data showed the potential blockbuster drug, SAGE-217, met the primary endpoint, although a serious adverse event was observed in both the drug and placebo arm, the company said on Monday.

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Sr. Manager, Regulatory Affairs, CMC
CytomX Therapeutics San Francisco, CA
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