Clinical trial
Efficacy, Safety and Tolerability of SPD485 in Children Aged 6-12 Diagnosed With…
NCT00151970 · Noven Therapeutics, Industry · Completed
Key facts
| NCT number | NCT00151970 |
|---|---|
| Title | Efficacy, Safety and Tolerability of SPD485 in Children Aged 6-12 Diagnosed With ADHD |
| Official title | A Phase IIB, Randomized, Double-blind, Multi-Center, Placebo-Controlled, Dose-Optimization, 3-way Cross-Over, Analog Classroom Study to Assess the Efficacy, Duration of Effect, Tolerability and Safety of 4- and 6- Hour Wear Times of Methylphenidate Transdermal System (MTS) in Pediatric Subjects Aged… |
| Lead sponsor | Noven Therapeutics, Industry |
| Collaborators | Noven Pharmaceuticals, Inc. Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Attention Deficit Disorder With Hyperactivity |
| Intervention type | Drug |
| Interventions | Methylphenidate Transdermal System, Placebo, Concerta |
| Enrollment | 128 |
| Start date | Jun 1, 2005 |
| Primary completion | Oct 1, 2006 |
| Completion | Oct 1, 2006 |
| First posted | Sep 9, 2005 |
| Last update posted | Jul 9, 2015 |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: