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CompletedNCT02009163

Maintenance of Efficacy of SPD489 for Binge Eating disorders

This study is completed in the United States, in Canada, in Germany, .... It is testing Maintenance of Efficacy of SPD489 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.

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In plain English

Key information made simple

What is this study testing?

This study is testing whether Lisdexamfetamine dimesylate may be useful for adults experiencing eating disorders.

What would participation involve?

Participants may receive Lisdexamfetamine dimesylate, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in Canada, in Germany, and in Spain.

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: January 27, 2014
Recruitment status
Completed
Enrollment listed in the registry
418
Sponsor
Shire
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug, OTHER
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States, Canada, Germany, ...
Age range
From 18 Years to 55 Years
Official registry ID
NCT02009163
Official title
A Phase 3, Multicenter, Double-blind, Placebo-controlled, Randomized-withdrawal Study to Evaluate the Maintenance of Efficacy of SPD489 in Adults Aged 18-55 Years With Moderate to Severe Binge Eating Disorder

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.

Canada · 2 sites
  • Anxiety and Mood Disorder Center
    Mississauga, Ontario
    Site status: Not listed — confirm with the team
  • Manna Research
    Pointe-Claire, Quebec
    Site status: Not listed — confirm with the team
Germany · 6 sites
  • Klinische Forschung Berlin-Mitte GmbH
    Berlin
    Site status: Not listed — confirm with the team
  • EMOVIS GmbH - Klinische Forschung
    Berlin
    Site status: Not listed — confirm with the team
  • Klinische Forschung Dresden GmbH
    Dresden
    Site status: Not listed — confirm with the team
  • Klinische Forschung Hannover-Mitte GmbH
    Hanover
    Site status: Not listed — confirm with the team
  • Forschung Schwerin GmbH, Friedrichstrasse 1
    Schwerin
    Site status: Not listed — confirm with the team
  • Studienzentrum Nordwest
    Westerstede
    Site status: Not listed — confirm with the team
Spain · 3 sites
  • Hospital de la Santa Creu I Sant Pau
    Barcelona
    Site status: Not listed — confirm with the team
  • Hospital Universitario Infanta Leonor
    Madrid
    Site status: Not listed — confirm with the team
  • Hospital del Henares
    Madrid
    Site status: Not listed — confirm with the team
Sweden · 3 sites
  • Lakarmottagningen Ekdahl & Kronberg
    Malmö
    Site status: Not listed — confirm with the team
  • Sofiahemmet
    Stockholm
    Site status: Not listed — confirm with the team
  • Stockholm Center for Eating Disorders
    Stockholm
    Site status: Not listed — confirm with the team
United States · 39 sites
  • Gulfcoast Clinical Research Center
    Fort Myers, Florida
    Site status: Not listed — confirm with the team
  • Innovative Clinical Research, Inc
    Lauderhill, Florida
    Site status: Not listed — confirm with the team
  • Compass Research LLC North Clinic
    Leesburg, Florida
    Site status: Not listed — confirm with the team
  • Florida Clinical Research Center, LLC
    Maitland, Florida
    Site status: Not listed — confirm with the team
  • Scientific Clinical Research, Inc
    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
  • NeuroTrials Research, Inc
    Atlanta, 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
    Indianapolis, Indiana
    Site status: Not listed — confirm with the team
  • Clinical Trials Technology, Inc
    Prairie Village, Kansas
    Site status: Not listed — confirm with the team
  • Cypress Medical Research Center
    Wichita, Kansas
    Site status: Not listed — confirm with the team
  • Louisiana Research Associates, Inc
    New Orleans, Louisiana
    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
  • Adams Clinical Trials, LLC
    Watertown, Massachusetts
    Site status: Not listed — confirm with the team
  • Rochester Center for Behavioral Medicine
    Rochester Hills, Michigan
    Site status: Not listed — confirm with the team
  • HBSA-Pacific Institute for Research & Evaluation
    Albuquerque, New Mexico
    Site status: Not listed — confirm with the team
  • Brooklyn Medical Institute
    Brooklyn, New York
    Site status: Not listed — confirm with the team
  • Wake Research Associates, LLC
    Raleigh, North Carolina
    Site status: Not listed — confirm with the team
  • Patient Priority Clinical Sites, LLC
    Cincinnati, Ohio
    Site status: Not listed — confirm with the team
  • Community Research
    Cincinnati, Ohio
    Site status: Not listed — confirm with the team
  • Midwest Clinical Research Center
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • Linder Center of Hope
    Mason, Ohio
    Site status: Not listed — confirm with the team
  • Oregon Center for Clinical Investigations, Inc (OCCI, Inc)
    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
  • Lehigh Center for Clinical Research
    Allentown, Pennsylvania
    Site status: Not listed — confirm with the team
  • Omega Medical Research
    Warwick, Rhode Island
    Site status: Not listed — confirm with the team
  • Radiant Research, Inc
    Anderson, South Carolina
    Site status: Not listed — confirm with the team
  • Radiant 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 Solution, Inc
    Memphis, Tennessee
    Site status: Not listed — confirm with the team
  • FutureSearch Clinical Trials, LP
    Austin, Texas
    Site status: Not listed — confirm with the team
  • FutureSearch Trials of Dallas, LP
    Dallas, 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
  • Research Across America
    Plano, Texas
    Site status: Not listed — confirm with the team
  • Radiant Research, Inc
    San Antonio, Texas
    Site status: Not listed — confirm with the team
  • Northwest Clinical Research Center
    Bellevue, Washington
    Site status: Not listed — confirm with the team
  • Summit Research Network (Seattle) LLC
    Seattle, Washington
    Site status: Not listed — confirm with the team

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Study ID: NCT02009163. We help you review the study, but cannot decide medical eligibility.
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 Lisdexamfetamine dimesylate, Placebo. 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 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 Shire, 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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