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CompletedNCT01101022

Safety study of SPD489 in ADHD

This study is completed in the United States. It is testing SPD489 for ADHD.

ADHDDrugFrom 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 SPD489 may be useful for adults experiencing ADHD.

What would participation involve?

Participants may receive SPD489, 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 ADHD.

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: May 19, 2010
Recruitment status
Completed
Enrollment listed in the registry
161
Sponsor
Shire
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug, OTHER
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
From 18 Years to 55 Years
Official registry ID
NCT01101022
Official title
A Phase 4, Randomized, Double-Blind, Multicenter, Placebo-controlled, Parallel Group Study Evaluating the Safety and Efficacy of SPD489 on Executive Function (Self-Regulation) Behaviors in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD) Reporting Clinically Significant Impairment of Real-World Executive Function Behavior.

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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 · 39 sites
  • Clinical Study Centers, LLC
    Little Rock, Arkansas
    Site status: Not listed — confirm with the team
  • Peninsula Research Assoc, Inc
    Rolling Hills Estates, California
    Site status: Not listed — confirm with the team
  • PCSD Feighner Research
    San Diego, California
    Site status: Not listed — confirm with the team
  • Florida Clinical Research Center, LLC
    Bradenton, Florida
    Site status: Not listed — confirm with the team
  • Gulfcoast Clinical Research Center
    Fort Myers, Florida
    Site status: Not listed — confirm with the team
  • Dr. George Joseph, MD and Associates PA
    Jacksonville Beach, Florida
    Site status: Not listed — confirm with the team
  • Florida Clinical Research Center, LLC
    Maitland, Florida
    Site status: Not listed — confirm with the team
  • CNS Healthcare
    Orlando, Florida
    Site status: Not listed — confirm with the team
  • Janus Center For Psychiatric Research
    West Palm Beach, Florida
    Site status: Not listed — confirm with the team
  • Atlanta Center For Medical Research
    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
  • AMR-BABER Research Inc.
    Naperville, Illinois
    Site status: Not listed — confirm with the team
  • Psychiatric Associates
    Overland Park, Kansas
    Site status: Not listed — confirm with the team
  • Vince and Associates Clinical Research, Inc.
    Overland Park, Kansas
    Site status: Not listed — confirm with the team
  • Four Rivers Clinical Research
    Paducah, Kentucky
    Site status: Not listed — confirm with the team
  • Mark Hertzman MD, PC
    Rockville, Maryland
    Site status: Not listed — confirm with the team
  • Rochester Center for Behavioral Medicine
    Rochester Hills, Michigan
    Site status: Not listed — confirm with the team
  • The Behavioral Medicine Clinic of NW Michigan, PC
    Traverse City, Michigan
    Site status: Not listed — confirm with the team
  • Midwest Research Group
    Saint Charles, Missouri
    Site status: Not listed — confirm with the team
  • Center for Psychiatry and Behavioral Medicine, Inc.
    Las Vegas, Nevada
    Site status: Not listed — confirm with the team
  • Center for Emotional Fitness
    Cherry Hill, 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
  • Mental Health and Addictive Disorders Research Program
    New York, New York
    Site status: Not listed — confirm with the team
  • Triangle Neuropsychiatry
    Durham, North Carolina
    Site status: Not listed — confirm with the team
  • Richard H. Weisler, MD, Pa & Associates
    Raleigh, North Carolina
    Site status: Not listed — confirm with the team
  • Oregon Center for Clinical Investigations, Inc.
    Portland, Oregon
    Site status: Not listed — confirm with the team
  • Occi, Inc (Oregon Center For Clinical Investigations, Inc.)
    Salem, Oregon
    Site status: Not listed — confirm with the team
  • FutureSearch Trials, LP
    Austin, Texas
    Site status: Not listed — confirm with the team
  • Bayou City Research, Ltd.
    Houston, Texas
    Site status: Not listed — confirm with the team
  • Red Oak Psychiatry Associates P.A.
    Houston, Texas
    Site status: Not listed — confirm with the team
  • John M. Turnbow, MD, PA
    Lubbock, Texas
    Site status: Not listed — confirm with the team
  • Vermont Clinical Study Center
    Burlington, Vermont
    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
  • Eastside Therapeutic Resource
    Kirkland, Washington
    Site status: Not listed — confirm with the team
  • Summit Research Network, LLC
    Seattle, Washington
    Site status: Not listed — confirm with the team
  • Rockwood Clinic
    Spokane, Washington
    Site status: Not listed — confirm with the team
  • Dean Foundation for Health, Research and Education
    Middleton, Wisconsin
    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 adhd. 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 SPD489, Placebo. Phase 4 studies usually happen after treatment approval, to monitor real-world use.

Who might this study be for?

This study may concern people with adhd; 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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