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CompletedNCT00880217

3 Dosages of JNJ-31001074 for ADHD

This study is completed in the United States. It is testing 3 Dosages of JNJ-31001074 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 Atomoxetine 80 mg/d may be useful for adults experiencing ADHD.

What would participation involve?

Participants may receive Atomoxetine 80 mg/d, 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 dateMay 2009
Recruitment status
Completed
Enrollment listed in the registry
430
Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Sponsor type
Pharmaceutical company
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
NCT00880217
Official title
A Randomized, Double-Blind, Placebo- and Active-Controlled, Parallel-Group, Multicenter Study of 3 Dosages of JNJ-31001074 in the Treatment of Adult Subjects With Attention-Deficit/Hyperactivity 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.

United States · 35 sites
  • Little Rock
    Little Rock, Arkansas
    Site status: Not listed — confirm with the team
  • Lafayette
    Lafayette, California
    Site status: Not listed — confirm with the team
  • Los Alamitos
    Los Alamitos, California
    Site status: Not listed — confirm with the team
  • Santa Ana
    Santa Ana, California
    Site status: Not listed — confirm with the team
  • Wildomar
    Wildomar, California
    Site status: Not listed — confirm with the team
  • Bradenton
    Bradenton, Florida
    Site status: Not listed — confirm with the team
  • Jacksonville
    Jacksonville, Florida
    Site status: Not listed — confirm with the team
  • North Miami
    North Miami, Florida
    Site status: Not listed — confirm with the team
  • Orlando
    Orlando, Florida
    Site status: Not listed — confirm with the team
  • South Miami
    South Miami, Florida
    Site status: Not listed — confirm with the team
  • St. Petersburg
    St. Petersburg, Florida
    Site status: Not listed — confirm with the team
  • Atlanta
    Atlanta, Georgia
    Site status: Not listed — confirm with the team
  • Boise
    Boise, Idaho
    Site status: Not listed — confirm with the team
  • Eagle
    Eagle, Idaho
    Site status: Not listed — confirm with the team
  • Libertyville
    Libertyville, Illinois
    Site status: Not listed — confirm with the team
  • Overland Park
    Overland Park, Kansas
    Site status: Not listed — confirm with the team
  • Prairie Village
    Prairie Village, Kansas
    Site status: Not listed — confirm with the team
  • Rochester Hills
    Rochester Hills, Michigan
    Site status: Not listed — confirm with the team
  • Saint Charles
    Saint Charles, Missouri
    Site status: Not listed — confirm with the team
  • Mount Kisco
    Mount Kisco, New York
    Site status: Not listed — confirm with the team
  • New York
    New York, New York
    Site status: Not listed — confirm with the team
  • Raleigh
    Raleigh, North Carolina
    Site status: Not listed — confirm with the team
  • Dayton
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • Oklahoma City
    Oklahoma City, Oklahoma
    Site status: Not listed — confirm with the team
  • Eugene
    Eugene, Oregon
    Site status: Not listed — confirm with the team
  • Portland
    Portland, Oregon
    Site status: Not listed — confirm with the team
  • Media
    Media, Pennsylvania
    Site status: Not listed — confirm with the team
  • Charleston
    Charleston, South Carolina
    Site status: Not listed — confirm with the team
  • Memphis
    Memphis, Tennessee
    Site status: Not listed — confirm with the team
  • Austin
    Austin, Texas
    Site status: Not listed — confirm with the team
  • Wharton
    Wharton, Texas
    Site status: Not listed — confirm with the team
  • Burlington
    Burlington, Vermont
    Site status: Not listed — confirm with the team
  • Herndon
    Herndon, Virginia
    Site status: Not listed — confirm with the team
  • Seattle
    Seattle, Washington
    Site status: Not listed — confirm with the team
  • Middleton
    Middleton, Wisconsin
    Site status: Not listed — confirm with the team

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Study ID: NCT00880217. 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 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 Atomoxetine 80 mg/d, Placebo, OROS methylphenidate HCl 54 mg/d, JNJ-31001074 3 mg/d, JNJ-31001074 1 mg/d, JNJ-31001074 10 mg/d. 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 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 Johnson & Johnson Pharmaceutical Research & Development, L.L.C., 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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