282
Participants
Start Date
September 30, 2004
Primary Completion Date
June 30, 2005
Study Completion Date
June 30, 2005
Methylphenidate Transdermal System
The primary objective of this study was to evaluate, under controlled conditions, the safety and efficacy of MTS compared to placebo with reference to CONCERTA
Placebo
The primary objective of this study was to evaluate, under controlled conditions, the safety and efficacy of MTS compared to placebo with reference to CONCERTA
Concerta
The primary objective of this study was to evaluate, under controlled conditions, the safety and efficacy of MTS compared to placebo with reference to CONCERTA
Lead Sponsor
Noven Therapeutics
INDUSTRY