A Phase 3, Open-label, Multicenter, 12-Month Safety and Tolerability Study of SPD489 in Preschool Children Aged 4-5 Years Diagnosed With Attention-deficit / Hyperactivity Disorder
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https://search.vivli.org/doiLanding/studies/PR00007903/isLanding
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资源简介:
The purpose of this study is to evaluate the long-term safety of SPD489 administered as a
daily morning dose (5, 10, 15, 20, and 30 mg/day) in preschool children diagnosed with
Attention-deficit/Hyperactivity Disorder (ADHD).
提供机构:
Vivli
创建时间:
2022-06-14



