Part A of the study is an open-label design with dosing of SAGE-217 for 14 days.
Part B of the study is a randomized, double-blind, parallel-group, placebo-controlled design. Eligible participants were randomized to SAGE-217 or placebo for 14 days.
This study was previously posted by Sage Therapeutics. In November 2023, sponsorship of the trial was transferred to Biogen.