A Phase 3, Randomized, Double-blind, Multi-center, Placebo Controlled, Dose-Optimization, Safety and Efficacy Study of SHP465 in Children and Adolescents Aged 6-17 Years With Attention-Deficit Hyperactivity Disorder (ADHD)
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https://search.vivli.org/doiLanding/studies/00006701/isLanding
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资源简介：
The study is designed to evaluate the efficacy and safety of SHP465 in the treatment of ADHD
in children and adolescents (aged 6-17 years). The primary objective of this study is to
evaluate the efficacy of SHP465 administered as a daily morning dose compared to placebo in
the treatment of children and adolescents (6-17 years of age inclusive) diagnosed with ADHD.
提供机构：
Vivli
创建时间：
2021-02-18
