drugset / Trial / NCT02494778

A Study Evaluating if Pridopidine is Safe, Efficacious, and Tolerable in Patients With Huntington's Disease

NCT02494778 ↗

Phase 2 Terminated 248 enrolled Prilenia
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to collect and assess long term data on the safety, tolerability, and efficacy of pridopidine in patients with Huntington's disease (HD).

Timeline

Start
2015-09-24
Primary completion
2018-01-12
Completion
2018-01-12

Outcome

Outcome not reported

Stopped: “This study served its purpose in providing considerable safety data.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Pridopidine Small molecule 45 mg Oral

Indications