Restless Legs Syndrome Clinical Trial
Official title:
ASP8825 Phase ⅡStudy—A Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of ASP8825 in Patients With Restless Legs Syndrome
To demonstrate the superiority of ASP8825 over placebo and the dose response in patients with restless legs syndrome
Three doses of ASP8825 are compared to placebo in efficacy and safety point of view in patients with restless legs syndrome ;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
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Recruiting |
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