NWP09 in Children With Attention Deficit Hyperactivity Disorder (ADHD)
Completed · Phase 3 · Has a placebo group
Conditions studied: Attention Deficit Hyperactivity Disorder
In brief
The safety and efficacy of a chewable formulation of extended-release methylphenidate will be studied in children with ADHD
Key facts
- Study ID
- NCT01654250
- Run by
- Pfizer
- People needed
- 90
- Starts
- 2012-07-01
- Expected to finish
- 2012-10-01
- Last updated by the study team
- 2016-02-03
Who can join
Age: 6 and older, up to 12. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Children aged 6 to 12 years with ADHD who require pharmacologic treatment for this condition
You may not qualify if…
- Other serious illnesses or conditions that would put the patient at particular risk for safety events or would interfere with treatment/assessment of ADHD
Where it is running
- Clinical Study Centers, LLC — Little Rock, Arkansas, United States
- Laboratory School — Huntington Beach, California, United States
- UC Irvine Child Development Center — Irvine, California, United States
- UC Irvine - Hewitt Hall — Irvine, California, United States
- Florida Clinical Research Center, LLC — Bradenton, Florida, United States
- Woodland Community Church (Laboratory School) — Bradenton, Florida, United States
- Center for Psychiatry and Behavioral Medicine, Inc. — Las Vegas, Nevada, United States
- Bayou City Research, Ltd. — Houston, Texas, United States
- Westex Clinical Investigations — Lubbock, Texas, United States
Full record on ClinicalTrials.gov
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