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CompletedNCT04753164

ACT-539313 for Binge-Eating disorders

This study is completed in the United States. It is testing ACT-539313 for Binge-Eating disorders.

Eating disorders, Binge-Eating disordersDrugFrom 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 Oral ACT-539313 may be useful for adults experiencing eating disorders.

What would participation involve?

Participants may receive Oral ACT-539313, 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 eating disorders.

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 dateStarted: February 16, 2021
Recruitment status
Completed
Enrollment listed in the registry
136
Sponsor
Idorsia Pharmaceuticals Ltd.
Sponsor type
Other organization
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 55 Years
Official registry ID
NCT04753164
Official title
Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel-group, Proof-of-concept Study to Evaluate the Efficacy and Safety of Oral ACT-539313 in the Treatment of Adults With Moderate to Severe Binge Eating 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 · 30 sites
  • Southern California Research
    Beverly Hills, California
    Site status: Not listed — confirm with the team
  • Wr-Pri, Llc
    Encino, California
    Site status: Not listed — confirm with the team
  • Collaborative Neuroscience Network (CNS)
    Garden Grove, California
    Site status: Not listed — confirm with the team
  • Syrentis Clinical Research
    Santa Ana, California
    Site status: Not listed — confirm with the team
  • Connecticut Clinical Research - Cromwell
    Cromwell, Connecticut
    Site status: Not listed — confirm with the team
  • Clinical Neurosciences Solutions
    Jacksonville, Florida
    Site status: Not listed — confirm with the team
  • Behavioral Clinical Research
    North Miami, Florida
    Site status: Not listed — confirm with the team
  • Clinical Neuroscience Solutions Inc
    Orlando, Florida
    Site status: Not listed — confirm with the team
  • NeuorTrials Research Inc
    Atlanta, Georgia
    Site status: Not listed — confirm with the team
  • Psych Atlanta P.C.
    Marietta, Georgia
    Site status: Not listed — confirm with the team
  • Capstone Clinical Research
    Libertyville, Illinois
    Site status: Not listed — confirm with the team
  • Collective Medical Research
    Prairie Village, Kansas
    Site status: Not listed — confirm with the team
  • Harvard Medical School - McLean Hospital
    Belmont, Massachusetts
    Site status: Not listed — confirm with the team
  • Boston Clinical Trials, Inc
    Boston, Massachusetts
    Site status: Not listed — confirm with the team
  • Precise Research Centers
    Flowood, Mississippi
    Site status: Not listed — confirm with the team
  • St. Charles Psychiatric Associates dba Midwest research group
    Saint Charles, Missouri
    Site status: Not listed — confirm with the team
  • M3 Wake Research
    Las Vegas, Nevada
    Site status: Not listed — confirm with the team
  • ActivMed Practices & Research, Inc.
    Portsmouth, New Hampshire
    Site status: Not listed — confirm with the team
  • ActivMed Practices & Research
    Portsmouth, New Hampshire
    Site status: Not listed — confirm with the team
  • Bioscience Research
    Mount Kisco, New York
    Site status: Not listed — confirm with the team
  • Manhattan Behavioral Medicine PLLC
    New York, New York
    Site status: Not listed — confirm with the team
  • The Medical Research Network
    New York, New York
    Site status: Not listed — confirm with the team
  • CTI Clinical Research Center
    Cincinnati, Ohio
    Site status: Not listed — confirm with the team
  • Patient Priority Clinical Sites
    Cincinnati, Ohio
    Site status: Not listed — confirm with the team
  • University of Cincinnati College of Medicine - Lindner Center of HOPE
    Mason, Ohio
    Site status: Not listed — confirm with the team
  • North Star Medical Research, LLC
    Middleburg Heights, Ohio
    Site status: Not listed — confirm with the team
  • IPS Research Company
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • Oregon Center For Clinical Inv.
    Portland, Oregon
    Site status: Not listed — confirm with the team
  • Oregon Center for Clinical Investigations, Inc. (OCCI, Inc.)
    Salem, Oregon
    Site status: Not listed — confirm with the team
  • Clinical Trials of Texas, Inc. (CTT)
    San Antonio, 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 eating disorders. 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 ACT-539313, 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 eating disorders; age range: From 18 Years to 55 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 Idorsia Pharmaceuticals Ltd., 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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