A Study to Assess the Safety and Efficacy of Oral LPCN 1154A in Women With Severe PPD
Public ClinicalTrials.gov record NCT06979544. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Randomized, Blinded, Placebo-Controlled Study to Evaluate the Saftey and Efficacy of Oral LPCN 1154A in Women With Postpartum Depression
Study identification
- NCT ID
- NCT06979544
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- Lipocine Inc.
- Industry
- Enrollment
- 90 participants
Conditions and interventions
Conditions
Interventions
- LPCN 1154A Drug
- Placebo Drug
Drug
Eligibility (public fields only)
- Age range
- 15 Years to 45 Years
- Sex
- Female
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jun 15, 2025
- Primary completion
- Jan 15, 2026
- Completion
- Feb 16, 2026
- Last update posted
- Feb 23, 2026
2025 – 2026
United States locations
- U.S. sites
- 18
- U.S. states
- 11
- U.S. cities
- 17
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Advanced Research Center | Anahiem | California | 92805 | — |
| Alliance Research Institute | Canoga Park | California | 91304 | — |
| MedOne Clinical Research, LLC | Miami | Florida | 33145 | — |
| D&H National Research Centers | Miami | Florida | 33155 | — |
| Meridian International Research | Miami Gardens | Florida | 33014 | — |
| Atlanta Behavioral Research | Atlanta | Georgia | 30338 | — |
| CenExel Research Center | Decatur | Georgia | 30030 | — |
| CenExel Research Center | Savannah | Georgia | 31405 | — |
| Clinical Research Prime | Idaho Falls | Idaho | 83404 | — |
| Cypress Medical Research Center, LLC | Kansas City | Kansas | 67226 | — |
| Best Clinical Trials | New Orleans | Louisiana | 70115 | — |
| Oasis Clinical Research | Las Vegas | Nevada | 89121 | — |
| Monroe Biomedical Research | Monroe | North Carolina | 28112 | — |
| Suburban Research Associates | Media | Pennsylvania | 19063 | — |
| Gadolin Research | Beaumont | Texas | 77702 | — |
| New Dawn Wellness and Medical Center | Houston | Texas | 77082 | — |
| Maximos OB/GYN | League City | Texas | 77573 | — |
| Populace Research | Provo | Utah | 84604 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06979544, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Feb 23, 2026 · Synced May 20, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06979544 live on ClinicalTrials.gov.