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CompletedNCT00531752

Two doses of PF-03654746 for ADHD in adults

About this title

A Study to Evaluate the Efficacy and Safety of Two Doses of PF-03654746 in Adults With Attention Deficit Hyperactivity Disorder (ADHD).

Read the official source — NCT00531752

Researchers compared PF-03654746 and placebo, tracking side effects to assess safety in adults with ADHD.

Medication studyAges 18–55United States
The study in practice

Understand this study

What did researchers investigate?

Researchers compared PF-03654746 and placebo, tracking side effects to assess safety in adults with ADHD.

Who was this study for?

This study was for people with ADHD. Listed age limits: 18 years to 55 years. Other eligibility criteria applied.

Listed locations
Lafayette and 6 more locationsSee all locations and recruitment
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Study clarity

Study information

Study start dateDecember 2007
Recruitment status
Completed
Enrollment listed in the registry
66
Sponsor
Pfizer
Sponsor type
Unknown or unclear
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
NCT00531752
Official title
Show the full official title

A Phase Iia, Randomized, Double Blind, Placebo Controlled, Three-treatment, Two-period Crossover Study Of The Efficacy And Safety Of Two Doses Of Pf-03654746 In Adults With Attention Deficit Hyperactivity Disorder

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Recruitment & locations

Completed

Lafayette · Los Alamitos · Newport Beach

4 more locations
  • Chicago
  • Cambridge
  • New York
  • Herndon
FAQ

Questions about this study

What did researchers investigate?

Researchers compared PF-03654746 and placebo, tracking side effects to assess safety in adults with ADHD.

Who is behind this study?

The study sponsor is Pfizer.

Did this study involve medication?

Yes. The study involved medication, including PF-03654746 and Placebo capsules.

Who was this study for?

This study was for people with ADHD. Listed age limits: 18 years to 55 years. Other eligibility criteria applied.

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