Trial Profile
A Placebo-Controlled, Double-Blind, Parallel-Group, Dose-Titration Study to Evaluate the Efficacy and Safety of CONCERTA (Methylphenidate HCl) Extended-Release Tablets in Adults With Attention Deficit Hyperactivity Disorder at Doses of 36 mg, 54 mg, 72 mg, 90 mg, or 108 mg Per Day.
Status:
Completed
Phase of Trial:
Phase III
Latest Information Update: 11 Feb 2010
Price :
$35
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At a glance
- Drugs Methylphenidate (Primary)
- Indications Attention-deficit hyperactivity disorder
- Focus Registrational; Therapeutic Use
- 17 Dec 2009 Patient numbers amended from 226 to 229 as reported by ClinicalTrials.gov.
- 12 Sep 2009 Secondary endpoints presented at 22nd Annual Congress of the European College of Neuropsychopharmacology (ECNP 2009).
- 19 Oct 2007 Status change from in progress to completed.