- Trials with a EudraCT protocol (1)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1 result(s) found for: 2007-002111-82.
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EudraCT Number: 2007-002111-82 | Sponsor Protocol Number: 42603ATT3013 | Start Date*: 2007-10-24 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V., Turnhoutseweg 30, B-2340 Beerse, Belgium | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study to Evaluate Efficacy and Safety of Prolonged Release (PR) OROSĀ® methylphenidate (54 and 72 mg/day) i... | |||||||||||||
Medical condition: Attention Deficit-Hyperactivity Disorder (ADHD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) NL (Completed) DK (Completed) FI (Completed) BE (Completed) GB (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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