ASP8825 - Study in Patients With Restless Legs Syndrome

Status Completed

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

Clinical Trial Details

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

View Details

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