A Phase 2, to Evaluating the Safety and Efficacy of Pridopidine Vs Placebo for Symptomatic Treatment in Patients With Huntington's Disease

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 2, DOSE-FINDING, RANDOMIZED, PARALLEL-GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY, EVALUATING THE SAFETY AND EFFICACY OF PRIDOPIDINE 45 MG, 67.5 MG, 90 MG, AND 112.5 MG TWICE-DAILY VERSUS PLACEBO FOR SYMPTOMATIC TREATMENT IN PATIENTS WITH HUNTINGTON'S DISEASE.

Intervention/treatment:
PRIDOPIDINE
Medical condition:
HUNTINGTON DISEASE
Protocol code:
TV7820-CNS-20002
Control number:
169707
Status:
Closed
Approved:
December 23, 2013
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT02006472
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
21 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Prilenia
Organization
Prilenia
Phone:
+972 775558
Extension 482
Sponsor
TEVA BRANDED PHARMACEUTICAL PRODUCTS R&D INC

Locations

British Columbia

Investigational Site 11035
Vancouver, British Columbia

Ontario

Investigational Site 11036
Toronto, Ontario
Investigational Site 11037
Ottawa, Ontario

Results

See the results from the trial NCT02006472. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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