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Clinical Trial Summary

To demonstrate the superiority of ASP8825 over placebo and the dose response in patients with restless legs syndrome


Clinical Trial Description

Three doses of ASP8825 are compared to placebo in efficacy and safety point of view in patients with restless legs syndrome ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00530530
Study type Interventional
Source Astellas Pharma Inc
Contact
Status Completed
Phase Phase 2
Start date September 2007
Completion date January 2009

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