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A Phase 4, Multicenter, 2-part Study Composed of a Randomized, Double-blind, Parallel-group, Placebo-controlled, Active-comparator, Dose-optimization Evaluation Followed by a 1-Year Open-label Evaluation to Assess the Safety and Efficacy of Guanfacine Hydrochloride Prolonged-release (SPD503) in Children and Adolescents Aged 6 to 17 Years With Attention-deficit/Hyperactivity Disorder

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Trial Profile

A Phase 4, Multicenter, 2-part Study Composed of a Randomized, Double-blind, Parallel-group, Placebo-controlled, Active-comparator, Dose-optimization Evaluation Followed by a 1-Year Open-label Evaluation to Assess the Safety and Efficacy of Guanfacine Hydrochloride Prolonged-release (SPD503) in Children and Adolescents Aged 6 to 17 Years With Attention-deficit/Hyperactivity Disorder

Status: Active, no longer recruiting
Phase of Trial: Phase IV

Latest Information Update: 18 Sep 2024

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At a glance

  • Drugs Guanfacine (Primary) ; Atomoxetine
  • Indications Attention-deficit hyperactivity disorder
  • Focus Therapeutic Use
  • Sponsors Shire; Shire Pharmaceutical Development; Takeda Development Center Americas

    • Most Recent Events

    • 18 Sep 2024 This trial is ongoing in Belgium, according to European Clinical Trials Database record.
    • 18 Sep 2024 This trial is ongoing in Belgium, according to European Clinical Trials Database record.
    • 14 Jun 2024 Status changed from recruiting to active, no longer recruiting.

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