drugset / Trial / NCT00269516

SLV308 for Treatment of Patients With Early Parkinson's Disease

NCT00269516 ↗

Phase 3 Completed 468 enrolled Solvay Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2006-06
Primary completion
2007-12
Completion
2007-12

Outcome

Met primary endpoint

paper Pardoprunox showed a significant benefit over placebo in the primary efficacy variable PMID 21542016 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Pardoprunox Small molecule 6 mg —
Subject Pardoprunox Small molecule 12 mg —
Subject Pardoprunox Small molecule 42 mg —

Indications