drugset / Trial / NCT03922711

A Study to Assess the Safety and Effectiveness of Pridopidine Compared to Placebo in the Treatment of Levodopa-Induced Dyskinesia in Patients With Parkinson's Disease

NCT03922711

Phase 2 Terminated 23 enrolled Prilenia
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, three-arm, parallel-group, double-blind, placebo-controlled, study to evaluate the efficacy, safety and pharmacokinetics (PK) of pridopidine vs. placebo for the treatment of Levodopa Induced Dyskinesia (LID) in patients with Parkinson Disease.

Timeline

Start
2019-05-22
Primary completion
2020-07-22
Completion
2020-07-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Pridopidine Small molecule Oral

Indications