A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
Status: | Completed |
---|---|
Conditions: | Depression, Depression, Women's Studies |
Therapuetic Areas: | Psychiatry / Psychology, Reproductive |
Healthy: | No |
Age Range: | 18 - 45 |
Updated: | 1/16/2019 |
Start Date: | December 2016 |
End Date: | December 11, 2018 |
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
This is a multicenter, randomized, double-blind, parallel-group, placebo-controlled study of
the efficacy, safety and pharmacokinetics of SAGE-217 in approximately 140 adult female
subjects diagnosed with severe postpartum depression.
the efficacy, safety and pharmacokinetics of SAGE-217 in approximately 140 adult female
subjects diagnosed with severe postpartum depression.
Key Inclusion Criteria:
- Subject either must have ceased lactating at screening or, if still lactating or
actively breastfeeding at screening, must agree to temporarily cease giving breast
milk to her infant(s)
- Subject has had a Major Depressive Episode that began no earlier than the third
trimester and no later than the first 4 weeks following delivery, as diagnosed by the
Structured Clinical Interview for DSM-5 Axis I Disorders (SCID-I)
- Subject is ≤ six months postpartum
Key Exclusion Criteria:
- Active psychosis
- Attempted suicide associated with current episode of postpartum depression
- Medical history of seizures
- Medical history of bipolar disorder, schizophrenia, and/or schizoaffective disorder.
Note: suicidal ideation is not an exclusion. Other protocol-defined inclusion/exclusion
criteria may apply.
We found this trial at
37
sites
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