drugset / Trial / NCT00988052

A Study To Evaluate the Long-Term Safety, Tolerability and Effect on Disease Course

NCT00988052

Phase 3 Terminated 839 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to make laquinimod 0.6 mg available for all subjects who completed the placebo-controlled MS-LAQ-301 study according to the protocol and to evaluate the long-term safety, tolerability and effect on disease course of daily oral laquinimod 0.6 mg in subjects with relapsing multiple sclerosis.

Timeline

Start
2009-11-10
Primary completion
2017-07-01
Completion
2017-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Laquinimod Small molecule 0.6 mg Oral

Indications