A Clinical Trial of Intravenous Ganaxolone in Women With Postpartum Depression
Status: | Recruiting |
---|---|
Conditions: | Depression, Depression, Psychiatric, Psychiatric, Psychiatric, Women's Studies |
Therapuetic Areas: | Psychiatry / Psychology, Reproductive |
Healthy: | No |
Age Range: | 18 - 45 |
Updated: | 10/4/2018 |
Start Date: | June 27, 2017 |
End Date: | June 30, 2019 |
Contact: | Jaakko Lappalainen, MD, PhD |
Email: | jlappalainen@marinuspharma.com |
Phone: | 484 801 4678 |
A Phase 2A, Double-blind, Placebo-controlled, Multiple-dose Escalation Study to Evaluate Safety, Pharmacokinetics and Efficacy of Intravenously Administered Ganaxolone in Women With Postpartum Depression
This study will evaluate the Safety, Pharmacokinetics and Efficacy of IV Administration of
Ganaxolone in Women with Postpartum Depression
Ganaxolone in Women with Postpartum Depression
Inclusion Criteria:
- Subject experienced a Major Depressive Episode, which started between the start of the
third trimester and 4 weeks following delivery. The Major Depressive Episode must be
diagnosed according to MINI 7.0 interview
- Subject gave birth in the last 6 months
- Subject has a HAMD17 score of ≥ 26 at screening
- Subject must agree to stop breastfeeding from start of study treatment or must agree
to temporarily cease giving breast milk to her infant(s)
Exclusion Criteria:
- Current or past history of any psychotic illness, including Major Depressive Episode
with psychotic features
- History of suicide attempt within the past 3 years
- Active suicidal ideation
- History of bipolar I disorder
- History of seizure disorder
We found this trial at
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