Study ID: LAQ-MS-201

Study Title

A Multinational, Randomized, Double-blind, ParFemale, Maleel-group, Placebo-controlled Study Assessing the Safety and Tolerability

Teva Identifier

LAQ-MS-201

ClinicalTrials.gov Identifier

NCT01404117

Study Status

Withdrawn

Trial Condition(s)

Relapsing Multiple Sclerosis

Interventions

Drug: Laquinimod 0.6 | Drug: Laquinimod 1.2 | Other: Glatiramer Acetate or interferon-beta+ Placebo

Study Description

Please refer to ClinicalTrials.gov for a description of the trial
ClinicalTrials.gov study records with inclusion and exclusion criteria
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Key Participation Requirements

Gender

Female, Male

Age Range

18 Years to 55 Years

Trial Duration

03/01/2012 - 01/01/2014

Phase

Phase 2

Study Type

Interventional