RE104 Safety and Efficacy Study in Postpartum Depression (NCT06342310) | Clinical Trial Compass
CompletedPhase 2
RE104 Safety and Efficacy Study in Postpartum Depression
United States84 participantsStarted 2024-06-14
Plain-language summary
The purpose of this study is to determine if treatment with a single dose of RE104 for Injection reduces depressive symptoms in participants with moderate-to-severe postpartum depression (PPD) as compared to active-placebo.
Who can participate
Age range18 Years – 45 Years
SexFEMALE
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Inclusion Criteria:
* Is ≤15 months postpartum at Screening.
* Meet DSM-5 criteria for postpartum depression (PPD): experiencing a major depressive episode that began at any time starting at the beginning of the second trimester (≥14 weeks) of pregnancy through 4 weeks post delivery.
* Has a Hamilton Depression Scale (HAM-D) total score meeting severity threshold at Screening and Baseline.
* Is not using any psychotropic medications or psychotherapy for 30 days prior to Screening, OR are on an already stable/established regimen of SSRIs or psychotherapy for 30 days prior to Screening.
* Has ceased breastfeeding at Screening.
* Has a negative pregnancy test at Screening and Day 0 prior to study drug administration.
Exclusion Criteria:
* History or active postpartum psychosis per Investigator assessment.
* History of treatment-resistant depression within the current postpartum depressive episode.
* Has a significant risk of suicide.
* Active or medical history of bipolar disorder, schizophrenia, schizoaffective disorder, psychotic disorder and/or borderline personality disorder, or first-degree family history of psychosis or bipolar disorder.
* Medically significant condition rendering unsuitability for the study .
* Has received electroconvulsive therapy (ECT) or transcranial magnetic stimulation within 90 days prior to Screening.
* Has used psychedelics such as psilocybin, ayahuasca, mescaline, or LSD (with the exception of cannabis) within 12 months prior to Screening.
* …
What they're measuring
1
RE104 30 mg versus RE104 1.5 mg change from baseline in MADRS total score