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A Multicentre, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study to Evaluate Efficacy and Safety of Prolonged Release (PR) OROS [oral-release osmotic system] Methylphenidate (54 and 72 mg/Day) in Adults With Attention Deficit/Hyperactivity Disorder

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Trial Profile

A Multicentre, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study to Evaluate Efficacy and Safety of Prolonged Release (PR) OROS [oral-release osmotic system] Methylphenidate (54 and 72 mg/Day) in Adults With Attention Deficit/Hyperactivity Disorder

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 06 Oct 2021

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At a glance

  • Drugs Methylphenidate (Primary)
  • Indications Attention-deficit hyperactivity disorder
  • Focus Therapeutic Use
  • Acronyms Lamda-2
  • Sponsors Janssen-Cilag

Most Recent Events

  • 24 Jun 2014 Planned primary completion date changed to 1 Apr 2009.
  • 14 Oct 2009 Actual end date (Apr 2009) added as reported by ClinicalTrials.gov.
  • 14 Oct 2009 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.

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