Clinical Study

Study Designed To Evaluate The Long-Term Safety And Efficacy Of Study Drug (Spd503) In Kids With Attention-Deficit/Hyperactivity Disorder

Posted Date: Jan 14, 2020

  • Investigator: Melissa Delbello
  • Specialties: ADD/ADHD, Psychiatry/Psychology
  • Type of Study: Drug

A Phase 4, Multicenter, 2-part Study Composed of a 1-Year 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

Criteria:

Kids Aged 6 To 17 Years Diagnosed With Adhd With Prior Stimulant Therapy Is Not Suitable, Not Tolerated

Keywords:

Add, Adhd, Children And Adolescents

For More Information:

Kelsey Reinhart, M.S.
(513) 558-3952
reinhakt@ucmail.uc.edu


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