A phase III, randomized, multi-center, double-blind, parallel-group, placebo-controlled safety and efficacy study of SPD503 [Intuniv; guanfacine] in children and adolescents aged 6-17 with attention-deficit/hyperactivity disorder (ADHD).

Trial Profile

A phase III, randomized, multi-center, double-blind, parallel-group, placebo-controlled safety and efficacy study of SPD503 [Intuniv; guanfacine] in children and adolescents aged 6-17 with attention-deficit/hyperactivity disorder (ADHD).

Completed
Phase of Trial: Phase III

Latest Information Update: 30 Nov 2009

At a glance

  • Drugs Guanfacine (Primary)
  • Indications Attention-deficit hyperactivity disorder
  • Focus Registrational; Therapeutic Use
  • Sponsors Shire
  • Most Recent Events

    • 07 May 2008 Results of a pooled analysis presented at APS 2008, according to a Shire media release.
    • 30 Jan 2008 Results have been published (1101050)
    • 23 May 2007 Results were reported at the APA 2007 conference.
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