Patient Guide: A Study to Assess the Safety and Efficacy of Oral LPCN 1154A in Women With Severe PPD

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 14 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06979544
Status: 🟢 Enrolling Now
Condition: Depression, Postpartum, Depression, Post-Partum, Postpartum Depression (PPD), Post-Natal Depression, Peripartum Depression, Postnatal Depression
Phase: PHASE3

Where You Can Participate

This study is available at 14 locations across the country.

Top locations include:
  • • Anahiem, California
  • • Canoga Park, California
  • • Miami Gardens, Florida
  • • And 11 more locations

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A Study to Assess the Safety and Efficacy of Oral LPCN 1154A in Women With Severe PPD - Join Clinical Trial NCTNCT06979544

How to Join This Clinical Trial - NCTNCT06979544

Learn how to participate in this PHASE3 trial studying an investigational therapy for Depression, Postpartum, Depression, Post-Partum, Postpartum Depression (PPD), Post-Natal Depression, Peripartum Depression, Postnatal Depression. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Depression, Postpartum, Depression, Post-Partum, Postpartum Depression (PPD), Post-Natal Depression, Peripartum Depression, Postnatal Depression. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Depression, Postpartum, Depression, Post-Partum, Postpartum Depression (PPD), Post-Natal Depression, Peripartum Depression, Postnatal Depression
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06979544 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 14 locations. Find a study site near you:

Clinical Research Site

Anahiem, California 92805 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Canoga Park, California 91304 - United States

Status: RECRUITING

Clinical Research Site

Miami Gardens, Florida 33014 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33145 - United States

Status: RECRUITING

Clinical Research Site

Atlanta, Georgia 30338 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Decatur, Georgia 30030 - United States

Status: RECRUITING

Clinical Research Site

Savannah, Georgia 31405 - United States

Status: RECRUITING

Clinical Research Site

Idaho Falls, Idaho 83404 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Kansas City, Kansas 67226 - United States

Status: RECRUITING

Clinical Research Site

New Orleans, Louisiana 70115 - United States

Status: RECRUITING

And 4 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Depression, Postpartum, Depression, Post-Partum, Postpartum Depression (PPD), Post-Natal Depression, Peripartum Depression, Postnatal Depression:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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