Trial Profile
A phase III, randomized, double-blind, multi-center, parallel-group, placebo-controlled safety and efficacy study of SPD503 [Intinuv; guanfacine] in children and adolescents aged 6-17 with attention deficit hyperactivity disorder (ADHD)
Status:
Completed
Phase of Trial:
Phase III
Latest Information Update: 14 Jun 2021
Price :
$35
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At a glance
- Drugs Guanfacine (Primary)
- Indications Attention-deficit hyperactivity disorder
- Focus Therapeutic Use
- Sponsors Shire
- 29 Jul 2018 Results of post hoc analysis of four studies (SPD503-301, SPD503-304, SPD503-312 and SPD503-316) published in the European Neuropsychopharmacology
- 20 Oct 2009 Atual number of patients (324) added as reported by ClinicalTrials.gov.
- 01 Feb 2009 Primary endpoint 'change from baseline to endpoint in Attention Deficit Hyperactivity Disorder Rating Scale' has been met.