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CompletedNCT02684279

Safety study of Dasotraline to Evaluate Long-term Safety and Tolerability in Binge Eating disorders

This study is completed in the United States. It is testing Dasotraline to Evaluate Long-term Safety and Tolerability for Binge Eating disorders.

Eating disorders, Binge Eating disordersDrugFrom 18 Years to 56 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 Dasotraline may be useful for adults experiencing eating disorders.

What would participation involve?

Participants may receive Dasotraline, attend study visits with the research team. 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 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 29, 2016
Recruitment status
Completed
Enrollment listed in the registry
533
Sponsor
Sumitomo Pharma America, Inc.
Sponsor type
Pharmaceutical company
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 56 Years
Official registry ID
NCT02684279
Official title
An Open-label, Flexibly-dosed, Multicenter, Extension Study of Dasotraline to Evaluate Long-term Safety and Tolerability in Adults With 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 · 57 sites
  • Noesis Parma
    Phoenix, Arizona
    Site status: Not listed — confirm with the team
  • Southern California Research
    Beverly Hills, California
    Site status: Not listed — confirm with the team
  • Pharmacology Research Institute
    Encino, California
    Site status: Not listed — confirm with the team
  • Collaborative NeuroScience Network Inc.
    Garden Grove, California
    Site status: Not listed — confirm with the team
  • Pharmacology Research Institute
    Newport Beach, California
    Site status: Not listed — confirm with the team
  • Artemis Institute for Clinical Research
    San Marcos, California
    Site status: Not listed — confirm with the team
  • Syrentis Clinical Research
    Santa Ana, California
    Site status: Not listed — confirm with the team
  • MCB Clinical Research Centers, LLC
    Colorado Springs, Colorado
    Site status: Not listed — confirm with the team
  • Weiss and Lytle, PLLC
    Denver, Colorado
    Site status: Not listed — confirm with the team
  • CT Clinical Research
    Cromwell, Connecticut
    Site status: Not listed — confirm with the team
  • Gulfcoast Clinical Research Center
    Fort Myers, Florida
    Site status: Not listed — confirm with the team
  • Clinical Neuroscience Solutions, Inc.
    Jacksonville, Florida
    Site status: Not listed — confirm with the team
  • Segal Institute for 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
  • Miami Research Associates
    South Miami, Florida
    Site status: Not listed — confirm with the team
  • Institute of Advanced Medical Research
    Alpharetta, Georgia
    Site status: Not listed — confirm with the team
  • Neuotrials Research, Inc.
    Atlanta, Georgia
    Site status: Not listed — confirm with the team
  • Northwest Behavioral Research Center
    Marietta, Georgia
    Site status: Not listed — confirm with the team
  • Capstone Clinical Research
    Libertyville, Illinois
    Site status: Not listed — confirm with the team
  • Goldpoint Clinical Research, Inc.
    Indianapolis, Indiana
    Site status: Not listed — confirm with the team
  • Phoenix Medical Research, Inc. Suite 135
    Prairie Village, Kansas
    Site status: Not listed — confirm with the team
  • Cyress Medical Research Center, LLC
    Wichita, Kansas
    Site status: Not listed — confirm with the team
  • McLean Hospital
    Belmont, Massachusetts
    Site status: Not listed — confirm with the team
  • Boston Clinical Trials
    Boston, Massachusetts
    Site status: Not listed — confirm with the team
  • ActivMed Practices & Research, Inc.
    Methuen, Massachusetts
    Site status: Not listed — confirm with the team
  • Adams Clinical Trials, LLC
    Watertown, Massachusetts
    Site status: Not listed — confirm with the team
  • St. Charles Psychiatric Associates - Midwest Research Group
    Saint Charles, Missouri
    Site status: Not listed — confirm with the team
  • ActivMed Practices and Research, Inc.
    Portsmouth, New Hampshire
    Site status: Not listed — confirm with the team
  • Center for Emotional Fitness
    Cherry Hill, New Jersey
    Site status: Not listed — confirm with the team
  • Princeton Medical Institute, LCC
    Princeton, New Jersey
    Site status: Not listed — confirm with the team
  • Bioscience Research, LLC
    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, LLC
    New York, New York
    Site status: Not listed — confirm with the team
  • Wake Research Associates
    Raleigh, North Carolina
    Site status: Not listed — confirm with the team
  • Radiant Research, Inc.
    Akron, Ohio
    Site status: Not listed — confirm with the team
  • Patient Priority Clinical Sites
    Cincinnati, Ohio
    Site status: Not listed — confirm with the team
  • Midwest Clinical Research Center
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • Lindner Center Of Hope
    Mason, Ohio
    Site status: Not listed — confirm with the team
  • IPS Research Company
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • Sunstone Medical Research, LLC
    Medford, Oregon
    Site status: Not listed — confirm with the team
  • Oregon Center for Clinical Investigatons, INC.
    Portland, Oregon
    Site status: Not listed — confirm with the team
  • Oregon Center for Clinical Investigations, Inc.
    Salem, Oregon
    Site status: Not listed — confirm with the team
  • Lehigh Center For Clinical Research
    Allentown, Pennsylvania
    Site status: Not listed — confirm with the team
  • Radiant Research, Inc.
    Anderson, South Carolina
    Site status: Not listed — confirm with the team
  • Radient Research, Inc.
    Greer, South Carolina
    Site status: Not listed — confirm with the team
  • Coastal Carolina Research Center
    Mt. Pleasant, South Carolina
    Site status: Not listed — confirm with the team
  • Clinical Neuroscience Solutons, Inc.
    Memphis, Tennessee
    Site status: Not listed — confirm with the team
  • Clinical Research Associates, Inc.
    Nashville, Tennessee
    Site status: Not listed — confirm with the team
  • Donald J. Garcia Jr., MD
    Austin, Texas
    Site status: Not listed — confirm with the team
  • Texas Center for Drug Development, Inc.
    Houston, Texas
    Site status: Not listed — confirm with the team
  • Psychiatric Medical Associates
    Plano, Texas
    Site status: Not listed — confirm with the team
  • Clinical Trials of Texas, Inc.
    San Antonio, Texas
    Site status: Not listed — confirm with the team
  • Radient Research, Inc.
    San Antonio, Texas
    Site status: Not listed — confirm with the team
  • Radiant Research, Inc.
    Murray, Utah
    Site status: Not listed — confirm with the team
  • Neuropsychiatric Associates
    Woodstock, Vermont
    Site status: Not listed — confirm with the team
  • NeuroScience, Inc.
    Herndon, Virginia
    Site status: Not listed — confirm with the team
  • Summitt Research Network(Seattle) LLC
    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 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 Dasotraline. 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 eating disorders; age range: From 18 Years to 56 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 Sumitomo Pharma America, Inc., which appears to be a pharmaceutical company. 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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