A Phase 2, Two-Part (Open-Label Followed by Double-Blind) Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of SAGE-217 in the Treatment of Adult Subjects With Moderate to Severe Major Depressive Disorder

Trial Profile

A Phase 2, Two-Part (Open-Label Followed by Double-Blind) Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of SAGE-217 in the Treatment of Adult Subjects With Moderate to Severe Major Depressive Disorder

Completed
Phase of Trial: Phase II

Latest Information Update: 15 Dec 2017

At a glance

  • Drugs SAGE 217 (Primary)
  • Indications Major depressive disorder
  • Focus Adverse reactions; Proof of concept; Therapeutic Use
  • Sponsors Sage Therapeutics
  • Most Recent Events

    • 07 Dec 2017 Results published in a Sage Therapeutics Media Release.
    • 07 Dec 2017 Primary endpoint the effect of treatment with SAGE-217 compared to placebo on depressive symptoms in patients with Major Depressive Disorder as assessed by the Hamilton Rating Scale for Depression (HAM-D) total score [Part B]) has been met according to a SAGE Therapeutics media release.
    • 30 Nov 2017 Status changed from active, no longer recruiting to completed.
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