drugset / Trial / NCT00202605

Safety and Efficacy of SPD465 in Adults With ADHD

NCT00202605 ↗

Phase 2 Completed 72 enrolled Shire
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of the study is to evaluate how safe and how well SPD465 works compared to placebo in adults with ADHD. It is hypothesized that SPD465 will achieve an extended duration of clinical benefit.

Timeline

Start
2005-09-29
Primary completion
2006-01-06
Completion
2006-01-06

Outcome

Met primary endpoint

paper PERMP total score significantly favored SHP465 MAS over placebo when averaged across all postdose assessments (19.29 [10.95, 27.63]; P < 0.0001) PMID 29087231 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject SPD465 Unknown 25 mg —