drugset / Trial / NCT00134251

Ascending Dose Tolerability/Safety of SLV308 for the Treatment of Parkinson's Disease

NCT00134251

Phase 3 Completed Solvay Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is a multicenter, randomized, double-blind, placebo controlled, parallel group study of a seven-week ascending dose period of SLV308 adjunctive to L-dopa treatment in patients with advanced stage Parkinson's disease (PD) and dose-dependent motor fluctuations. Patients (outpatients) will be randomized to one of three different treatment arms.

Timeline

Start
2005-10
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Pardoprunox Small molecule

Indications