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CompletedNCT02109562

RBP-7000 for schizophrenia

This study is completed in the United States. It is testing RBP-7000 for schizophrenia.

SchizophreniaDrugFrom 18 Years to 55 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 RBP-7000 may be useful for adults experiencing schizophrenia.

What would participation involve?

Participants may receive RBP-7000, 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 adults with schizophrenia.

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.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    Where are visits, can any be remote, and how much time is needed?

  • Costs and support

    What costs, reimbursement or compensation apply?

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateApril 2014
Recruitment status
Completed
Enrollment listed in the registry
354
Sponsor
Indivior Inc.
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 18 Years to 55 Years
Official registry ID
NCT02109562
Official title
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of RBP-7000 as a Treatment in Subjects With Acute Schizophrenia Over 8 Weeks (2 Subcutaneous Doses)

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Check recruitment and locations

Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.

View official study record (opens in a new tab)

The overall study status can differ from each site's status. Open a country to see its locations and their registry status.

United States · 32 sites
  • Woodland International Research Group, Inc.
    Little Rock, Arkansas
    Site status: Not listed — confirm with the team
  • Woodland International Research Group, Inc.
    Springdale, Arkansas
    Site status: Not listed — confirm with the team
  • Comprehensive Clinical Development - Cerritos, CA
    Cerritos, California
    Site status: Not listed — confirm with the team
  • Synergy Clinical Research of Escondido
    Escondido, California
    Site status: Not listed — confirm with the team
  • Behavioral Research Specialists, LLC
    Glendale, California
    Site status: Not listed — confirm with the team
  • Collaborative Neuroscience Networks, Inc.
    Long Beach, California
    Site status: Not listed — confirm with the team
  • Apostle Clinical Trials, Inc.
    Long Beach, California
    Site status: Not listed — confirm with the team
  • Pacific Research Partners
    Oakland, California
    Site status: Not listed — confirm with the team
  • Excell Research, Inc.
    Oceanside, California
    Site status: Not listed — confirm with the team
  • CNRI- Los Angeles, LLC
    Pico Rivera, California
    Site status: Not listed — confirm with the team
  • CNRI - San Diego, LLC
    San Diego, California
    Site status: Not listed — confirm with the team
  • Innovative Clinical Research
    Fort Lauderdale, Florida
    Site status: Not listed — confirm with the team
  • Behavioral Clinical Research, Inc.
    North Miami, Florida
    Site status: Not listed — confirm with the team
  • Florida Clinical Research Center, LLC
    Orlando, Florida
    Site status: Not listed — confirm with the team
  • Uptown Research Institute
    Chicago, Illinois
    Site status: Not listed — confirm with the team
  • Alexian Brothers Behavioral Health Hospital
    Hoffman Estates, Illinois
    Site status: Not listed — confirm with the team
  • Via Christi Research
    Wichita, Kansas
    Site status: Not listed — confirm with the team
  • Lake Charles Clinical Trials, LLC
    Lake Charles, Louisiana
    Site status: Not listed — confirm with the team
  • J. Gary Booker, MD, APMC
    Shreveport, Louisiana
    Site status: Not listed — confirm with the team
  • St. Louis Clinical Trials
    St Louis, Missouri
    Site status: Not listed — confirm with the team
  • PsychCare Consultants Research
    St Louis, Missouri
    Site status: Not listed — confirm with the team
  • Altea Research Institute
    Las Vegas, Nevada
    Site status: Not listed — confirm with the team
  • CRI Lifetree
    Marlton, New Jersey
    Site status: Not listed — confirm with the team
  • Neurobehavioral Research, Inc.
    Cedarhurst, New York
    Site status: Not listed — confirm with the team
  • New Hope Clinical Research
    Charlotte, North Carolina
    Site status: Not listed — confirm with the team
  • Midwest Clinical Research Center, LLC
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • Oklahoma Clinical Research Center
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • CRI Lifetree
    Philadelphia, Pennsylvania
    Site status: Not listed — confirm with the team
  • FutureSearch Clinical Trials, L.P.
    Austin, Texas
    Site status: Not listed — confirm with the team
  • Community Clinical Research, Inc.
    Austin, Texas
    Site status: Not listed — confirm with the team
  • FutureSearch Clinical Trials, L.P.
    Dallas, Texas
    Site status: Not listed — confirm with the team
  • Pillar Clinic Research, LLC
    Dallas, Texas
    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 schizophrenia. 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 RBP-7000, Placebo, Risperidone. 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 schizophrenia; age range: From 18 Years to 55 Years. The criteria appear fairly specific, 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 Indivior 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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