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A Multicentre, Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study To Evaluate the Safety And Efficacy Of Prolonged Release OROS Methylphenidate Hydrochloride (18, 36 and 72 mg/Day), With Open-Label Extension, In Adults With Attention Deficit/Hyperactivity Disorder.

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A Multicentre, Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study To Evaluate the Safety And Efficacy Of Prolonged Release OROS Methylphenidate Hydrochloride (18, 36 and 72 mg/Day), With Open-Label Extension, In Adults With Attention Deficit/Hyperactivity Disorder.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 31 Dec 2021

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At a glance

  • Drugs Methylphenidate (Primary)
  • Indications Attention-deficit hyperactivity disorder
  • Focus Registrational; Therapeutic Use
  • Acronyms LAMDA
  • Sponsors Janssen Pharmaceutica

    • Most Recent Events

    • 26 Apr 2011 Results assessing daily functioning and health-related quality of life published in the World Journal of Biological Psychiatry.
    • 22 Sep 2009 Actual patient number (402) added as reported by ClinicalTrials.gov.
    • 19 Oct 2007 Status changed from in progress to completed.

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