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CompletedNCT02651584

Once-Weekly and Once-Monthly, Long-Acting Subcutaneous Injectable Depot of Buprenorphine for Opioid Use Disorders

This study is completed in the United States. It is testing Once-Weekly and Once-Monthly, Long-Acting Subcutaneous Injectable Depot of Buprenorphine for Opioid Use Disorders.

Addiction, Opioid Use DisordersDrugFrom 18 Years to 65 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.

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In plain English

Key information made simple

What is this study testing?

This study is testing whether CAM2038 SC injection may be useful for adults experiencing addiction.

What would participation involve?

Participants may receive CAM2038 SC injection, 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 addiction.

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 dateDecember 2015
Recruitment status
Completed
Enrollment listed in the registry
428
Sponsor
Braeburn Pharmaceuticals
Sponsor type
Unknown or unclear
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 65 Years
Official registry ID
NCT02651584
Official title
A Phase III, Randomized, Double-Blind, Active-Controlled, Parallel Group, Multi-center Trial Assessing the Efficacy and Safety of a Once-Weekly and Once-Monthly, Long-Acting Subcutaneous Injectable Depot of Buprenorphine (CAM2038) in Treatment of Adult Outpatients With Opioid Use Disorder

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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 · 36 sites
  • Parkway Medical Center
    Birmingham, Alabama
    Site status: Not listed — confirm with the team
  • Haleyville Clinical Research LLC
    Haleyville, Alabama
    Site status: Not listed — confirm with the team
  • Boyett Health Services Inc
    Hamilton, Alabama
    Site status: Not listed — confirm with the team
  • Synergy East
    Lemon Grove, California
    Site status: Not listed — confirm with the team
  • North County Clinical Research
    Oceanside, California
    Site status: Not listed — confirm with the team
  • Asclepes Research
    Panorama City, California
    Site status: Not listed — confirm with the team
  • Artemis Institute for Clinical Research
    San Diego, California
    Site status: Not listed — confirm with the team
  • Care Practice
    San Francisco, California
    Site status: Not listed — confirm with the team
  • Synergist Research
    West Hollywood, California
    Site status: Not listed — confirm with the team
  • Dr Vijapura and Associates
    Jacksonville, Florida
    Site status: Not listed — confirm with the team
  • Innovative Clinical Research Inc
    Lauderhill, Florida
    Site status: Not listed — confirm with the team
  • TRY Research
    Maitland, Florida
    Site status: Not listed — confirm with the team
  • Tellus Clinical Research, Inc.
    Miami, Florida
    Site status: Not listed — confirm with the team
  • Scientific Clinical Research, Inc.
    North Miami, Florida
    Site status: Not listed — confirm with the team
  • Professional Research Network of Kansas, LLC
    Wichita, Kansas
    Site status: Not listed — confirm with the team
  • University of Kentucky Medical Center
    Lexington, Kentucky
    Site status: Not listed — confirm with the team
  • Stanley Street Treatment and Resources Inc
    Fall River, Massachusetts
    Site status: Not listed — confirm with the team
  • Novex Clinical Research
    New Bedford, Massachusetts
    Site status: Not listed — confirm with the team
  • Precise Research Centers
    Flowood, Mississippi
    Site status: Not listed — confirm with the team
  • PsychCare Consultants Research
    St Louis, Missouri
    Site status: Not listed — confirm with the team
  • St. Louis Clinical Trials
    St Louis, Missouri
    Site status: Not listed — confirm with the team
  • Wellness and Research Center
    Belvidere, New Jersey
    Site status: Not listed — confirm with the team
  • Comprehensive Clinical Research
    Berlin, New Jersey
    Site status: Not listed — confirm with the team
  • STARS/Columbia University
    New York, New York
    Site status: Not listed — confirm with the team
  • Neuro-Behavioral Clinical Research Center
    Canton, Ohio
    Site status: Not listed — confirm with the team
  • Midwest Clinical Research Center
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • North Star Medical Research
    Middleburg Heights, Ohio
    Site status: Not listed — confirm with the team
  • Rivus Wellness & Research Institute
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • Frost Medical Group
    Conshohocken, Pennsylvania
    Site status: Not listed — confirm with the team
  • The University of Pennsylvania Health System Treatment Research Center
    Philadelphia, Pennsylvania
    Site status: Not listed — confirm with the team
  • Lincoln Research
    Lincoln, Rhode Island
    Site status: Not listed — confirm with the team
  • Carolina Clinical Trials, Inc
    Charleston, South Carolina
    Site status: Not listed — confirm with the team
  • InSite Clinical Research
    Dallas, Texas
    Site status: Not listed — confirm with the team
  • Aspen Clinical Research
    Orem, Utah
    Site status: Not listed — confirm with the team
  • University of Vermont
    Burlington, Vermont
    Site status: Not listed — confirm with the team
  • Swedish Health Services
    Seattle, Washington
    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 addiction. 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 CAM2038 SC injection, SL BPN/NX tabs, placebo SC injections, SL placebo tablets. Phase 3 studies are usually larger and aim to confirm effectiveness and safety in a broader group.

Are there criteria about substance use or wanting to reduce it?

The public registry appears to mention tobacco, nicotine, alcohol, cannabis, or another addiction-related topic. Ask the study team whether you need to want to stop, reduce, already be abstinent, or simply meet use-related criteria. Eligibility must be confirmed by the study team.

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 Braeburn Pharmaceuticals, which appears to be unknown or unclear. 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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