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Clinical Trial Summary

This study is a multicenter, randomized, double blind, parallel group study of 6 months' treatment with SLV308 administered as a monotherapy in patients with early stage PD. An open label safety extension to this study is planned as a separate protocol for patients who are willing and eligible to participate.


Clinical Trial Description

n/a


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 NCT00269516
Study type Interventional
Source Solvay Pharmaceuticals
Contact
Status Completed
Phase Phase 3
Start date June 2006
Completion date December 2007

See also
  Status Clinical Trial Phase
Completed NCT00623324 - The Effects of Aplindore on the Treatment of Signs and Symptoms of Parkinson's Disease Phase 2
Completed NCT00332917 - An Open Label SLV308 Safety Extension to Study S308.3.001 in Early PD Patients Phase 3
Completed NCT00335374 - An Open Label SLV308 Safety Extension to Study S308.3.003 in Early PD Patients Phase 3
Completed NCT00599196 - An Open-Label Extension Trial to Assess the Safety of Long-Term Treatment of Rotigotine in Early-Stage Parkinson's Disease Phase 3