Brexpiprazole for PTSD
This study is completed in the United States. It is testing brexpiprazole for PTSD.
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.
Check recruitment and locations
Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability 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 · 54 sites
- Investigational SiteTuscaloosa, AlabamaSite status: Not listed — confirm with the team
- Investigational SitePhoenix, ArizonaSite status: Not listed — confirm with the team
- Investigational SiteLittle Rock, ArkansasSite status: Not listed — confirm with the team
- Investigational SiteRogers, ArkansasSite status: Not listed — confirm with the team
- Investigational SiteBellflower, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteBeverly Hills, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteGlendale, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteNational City, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteOceanside, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteOceanside, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteOrange, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteRedlands, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteRiverside, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteSan Diego, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteSan Marcos, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteTorrance, CaliforniaSite status: Not listed — confirm with the team
- Investigational SiteColorado Springs, ColoradoSite status: Not listed — confirm with the team
- Investigational SiteBradenton, FloridaSite status: Not listed — confirm with the team
- Investigational SiteFort Lauderdale, FloridaSite status: Not listed — confirm with the team
- Investigational SiteFort Myers, FloridaSite status: Not listed — confirm with the team
- Investigational SiteGainesville, FloridaSite status: Not listed — confirm with the team
- Investigational SiteJacksonville, FloridaSite status: Not listed — confirm with the team
- Investigational SiteNorth Miami, FloridaSite status: Not listed — confirm with the team
- Investigational SiteOrlando, FloridaSite status: Not listed — confirm with the team
- Investigational SiteOrlando, FloridaSite status: Not listed — confirm with the team
- Investigational SiteTampa, FloridaSite status: Not listed — confirm with the team
- Investigational SiteAtlanta, GeorgiaSite status: Not listed — confirm with the team
- Investigational SiteDecatur, GeorgiaSite status: Not listed — confirm with the team
- Investigational SiteRoswell, GeorgiaSite status: Not listed — confirm with the team
- Investigational SiteChicago, IllinoisSite status: Not listed — confirm with the team
- Investigational SiteSt Louis, MissouriSite status: Not listed — confirm with the team
- Investigational SiteLas Vegas, NevadaSite status: Not listed — confirm with the team
- Investigational SiteBerlin, New JerseySite status: Not listed — confirm with the team
- Investigational SitePrinceton, New JerseySite status: Not listed — confirm with the team
- Investigational SiteBrooklyn, New YorkSite status: Not listed — confirm with the team
- Investigational SiteCedarhurst, New YorkSite status: Not listed — confirm with the team
- Investigational SiteNew York, New YorkSite status: Not listed — confirm with the team
- Investigational SiteRochester, New YorkSite status: Not listed — confirm with the team
- Investigational SiteCharlotte, North CarolinaSite status: Not listed — confirm with the team
- Investigational SiteRaleigh, North CarolinaSite status: Not listed — confirm with the team
- Investigational SiteCincinnati, OhioSite status: Not listed — confirm with the team
- Investigational SiteOklahoma City, OklahomaSite status: Not listed — confirm with the team
- Investigational SiteOklahoma City, OklahomaSite status: Not listed — confirm with the team
- Investigational SitePortland, OregonSite status: Not listed — confirm with the team
- Investigational SiteSalem, OregonSite status: Not listed — confirm with the team
- Investigational SiteMedia, PennsylvaniaSite status: Not listed — confirm with the team
- Investigational SiteNorristown, PennsylvaniaSite status: Not listed — confirm with the team
- Investigational SiteLincoln, Rhode IslandSite status: Not listed — confirm with the team
- Investigational SiteCharleston, South CarolinaSite status: Not listed — confirm with the team
- Investigational SiteMemphis, TennesseeSite status: Not listed — confirm with the team
- Investigational SiteBellaire, TexasSite status: Not listed — confirm with the team
- Investigational SiteSan Antonio, TexasSite status: Not listed — confirm with the team
- Investigational SiteWichita Falls, TexasSite status: Not listed — confirm with the team
- Investigational SiteEverett, WashingtonSite status: Not listed — confirm with the team
Key information made simple
This summary needs review. Please check the official study record and contact the research team for details.
Your next step
Study sites are listed in the registry. Recruitment status can differ between sites. Ask the research team to confirm the location, any in-person visits, time commitment, costs or compensation, and participation criteria.
Questions to ask before joining
- What are the exact eligibility criteria, and what could exclude someone?
- How many visits, assessments, or follow-ups are expected, and over what period?
- What risks, side effects, practical burdens, or alternatives should be understood first?
- Who should be contacted to confirm locations, timing, compensation, and next steps?
Things to check before joining
- Recruitment status
- Completed
- Enrollment listed in the registry
- 336
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc.
- Sponsor type
- Pharmaceutical company
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
- Locations
- United States
- Age range
- From 18 Years to 65 Years
- Official registry ID
- NCT03033069
- Official title
- A Phase 2, Multicenter, Randomized, Double-blind, Placebo- and Active-controlled Trial of Brexpiprazole (1 - 3 mg/Day) as Monotherapy or as Combination Therapy in the Treatment of Adults With Post-traumatic Stress Disorder
- Official source
- Official registry link
Want help reviewing this study?
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.
Not medical advice
Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com
Questions about this study
What is this study trying to understand?
Based on the public registry summary, this study is trying to understand: To evaluate the safety, efficacy and tolerability of brexpiprazole (with placebo) as monotherapy or combination therapy with Zoloft (sertraline) in adults with PTSD. The study team can confirm the exact objective and what it means for you.
Does this study involve a medication?
This appears to be a medication / drug study involving Brexpiprazole, Sertraline, Brexpiprazole Matching Placebo, Sertraline Matching Placebo. Phase 2 studies usually explore whether the intervention may work, while continuing to monitor safety.
Who might this study be for?
This study may concern people with ptsd; age range: From 18 Years to 65 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 Otsuka Pharmaceutical Development & Commercialization, Inc., which appears to be a pharmaceutical company. Sponsor website: https://www.otsuka.co.jp/en/. 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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