Clinical trial
Efficacy and Safety of SPD465 in Adults With ADHD
NCT00150579 · Shire, Industry · Completed
Key facts
| NCT number | NCT00150579 |
|---|---|
| Title | Efficacy and Safety of SPD465 in Adults With ADHD |
| Official title | A Phase III, Randomized, Double-blind, Multi-center, Placebo-Controlled, Parallel-Group, Safety and Efficacy Study of SPD465 in Adults With Attention-Deficit Hyperactivity Disorder (ADHD). |
| Lead sponsor | Shire, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Attention Deficit Disorder With Hyperactivity |
| Intervention type | Drug |
| Interventions | Neutral salts of dextroamphetamine sulfate, USP, amphetamine sulfate, d-amphetamine saccharate, d, l-amphetamine aspartate monohydrate |
| Enrollment | 240 |
| Start date | Jan 27, 2005 |
| Primary completion | Jun 14, 2005 |
| Completion | Jun 14, 2005 |
| First posted | Sep 8, 2005 |
| Last update posted | Jun 30, 2021 |
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: