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Dataset from Open Label Extension Study With Pramipexole (PPX) in Children With Tourette Syndrome

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NIAID Data Ecosystem2026-05-02 收录
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https://doi.org/10.25934/00003521
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The primary objective of this open-label, flexible dose study is to assess the safety and efficacy of pramipexole over a 24-week period in children and adolescents (age 6-17 years inclusive) diagnosed with Tourette Syndrome according to Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) criteria and who have completed either Study 248.641 (NCT 00681863) or 248.644 (NCT 00558467).
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2024-11-26
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