An Open Label, Multicentre Study to Evaluate the Long Term Safety of Prolonged Release (PR) OROS Methylphenidate (18, 36, 54, 72 and 90 mg/day) in Adults with Attention Deficit/Hyperactivity Disorder

Mise à jour : Il y a 4 ans
Référence : EUCTR2005-004037-18

Femme et Homme

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Extrait

The primary objective of the open label study is to assess long term safety and tolerability of PR OROS methylphenidate in a flexible dose regimen (18-90 mg/day) in adult subjects diagnosed with ADHD.


Critère d'inclusion

  • Attention-Deficit/Hyperactivity Disorder (ADHD)