A Blinded, Study Saftey and Efficacy of Oral LPCN 1154A in Women With Postpartum Depression
This study is completed in the United States. It is testing Saftey and Efficacy of Oral LPCN 1154A for depression.
DepressionDrugFrom 15 Years to 45 Years
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
Then choose your country and confirm availability with each study site.
In plain English
Key information made simple
What is this study testing?
This study is testing whether LPCN 1154A may be useful for people experiencing depression.
What would participation involve?
Participants may receive LPCN 1154A, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in the United States.
Who is it mainly for?
This study appears to be mainly for people with depression.
What should you check before joining?
Ask about the dose, safety monitoring, and possible side effects, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.
Your next step
Check the study details
Check the official source, then confirm these points with the research team.
The overall study status can differ from each site's status. Open a country to see its locations and their registry status.
United States · 18 sites
Advanced Research Center
Anahiem, California
Site status: Not listed — confirm with the team
Alliance Research Institute
Canoga Park, California
Site status: Not listed — confirm with the team
MedOne Clinical Research, LLC
Miami, Florida
Site status: Not listed — confirm with the team
D&H National Research Centers
Miami, Florida
Site status: Not listed — confirm with the team
Meridian International Research
Miami Gardens, Florida
Site status: Not listed — confirm with the team
Atlanta Behavioral Research
Atlanta, Georgia
Site status: Not listed — confirm with the team
CenExel Research Center
Decatur, Georgia
Site status: Not listed — confirm with the team
CenExel Research Center
Savannah, Georgia
Site status: Not listed — confirm with the team
Clinical Research Prime
Idaho Falls, Idaho
Site status: Not listed — confirm with the team
Cypress Medical Research Center, LLC
Kansas City, Kansas
Site status: Not listed — confirm with the team
Best Clinical Trials
New Orleans, Louisiana
Site status: Not listed — confirm with the team
Oasis Clinical Research
Las Vegas, Nevada
Site status: Not listed — confirm with the team
Monroe Biomedical Research
Monroe, North Carolina
Site status: Not listed — confirm with the team
Suburban Research Associates
Media, Pennsylvania
Site status: Not listed — confirm with the team
Gadolin Research
Beaumont, Texas
Site status: Not listed — confirm with the team
New Dawn Wellness and Medical Center
Houston, Texas
Site status: Not listed — confirm with the team
Maximos OB/GYN
League City, Texas
Site status: Not listed — confirm with the team
Populace Research
Provo, Utah
Site status: Not listed — confirm with the team
In practice
For you
Participation may contribute to research. Personal benefit is not guaranteed.
Ask the research team to explain the activities, time commitment, and follow-up involved.
Study sites are listed. Confirm the relevant site and any travel before making plans.
Important
Not medical advice
Information from public sources.
Are you the study sponsor? Contact us to update this page: hi@hopestage.com
FAQ
Questions about this study
What is this study trying to understand?
This study is exploring medication or study treatment for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.
Does this study involve a medication?
This appears to be a medication / drug study involving LPCN 1154A, Placebo. Phase 3 studies are usually larger and aim to confirm effectiveness and safety in a broader group.
Who might this study be for?
This study may concern people with depression; age range: From 15 Years to 45 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may need to take a study treatment and have regular medical follow-up. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
What side effects, interactions, or treatment changes should I check?
If the study involves a medication, ask whether it is already approved, experimental, or being tested for a new use. Check possible side effects, interactions with current treatment, dose changes, monitoring, and what happens if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by Lipocine Inc., which appears to be another type of organization. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
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