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Terminated Phase 3 Interventional Results available

A Study to Evaluate the Long-term Safety, Tolerability and Effect of Daily Oral Laquinimod 0.6 mg on Disease Course in Subjects With Relapsing Multiple Sclerosis

ClinicalTrials.gov ID: NCT01047319

Public ClinicalTrials.gov record NCT01047319. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 6:32 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multinational, Multicenter, Open-label, Single-assignment Extension of the MS-LAQ-302 (BRAVO) Study, 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

Study identification

NCT ID
NCT01047319
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
1,047 participants

Conditions and interventions

Interventions

  • Laquinimod Drug

Drug

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 26, 2010
Primary completion
Jun 29, 2017
Completion
Jun 29, 2017
Last update posted
Dec 8, 2021

2010 – 2017

United States locations

U.S. sites
22
U.S. states
16
U.S. cities
21
Facility City State ZIP Site status
Teva Investigational Site 1267 Homewood Alabama 35209
Teva Investigational Site 1237 Phoenix Arizona 85013
Teva Investigational Site 1279 Phoenix Arizona 85018
Teva Investigational Site 1276 Tucson Arizona 85704
Teva Investigational Site 1272 Pasadena California 91105
Teva Investigational Site 1238 Sacramento California 95817
Teva Investigational Site 1280 Aurora Colorado 80045
Teva Investigational Site 1282 Sarasota Florida 34233
Teva Investigational Site 1275 Atlanta Georgia 30309
Teva Investigational Site 1250 Peoria Illinois 61603
Teva Investigational Site 1260 Indianapolis Indiana 46202
Teva Investigational Site 1263 Shreveport Louisiana 71103
Teva Investigational Site 1269 Baltimore Maryland 21201
Teva Investigational Site 1273 Albany New York 12205
Teva Investigational Site 1264 Amherst New York 14226
Teva Investigational Site 1261 Akron Ohio 44320
Teva Investigational Site 1245 Cleveland Ohio 44195-5244
Teva Investigational Site 1247 Columbus Ohio 43221
Teva Investigational Site 1244 Portland Oregon 97225
Teva Investigational Site 1281 Nashville Tennessee 37205
Teva Investigational Site 1270 Roanoke Virginia 24018
Teva Investigational Site 1253 Tacoma Washington 98405

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 122 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01047319, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 8, 2021 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01047319 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →