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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 Oct 21, 2026, 4:55 AM 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To make laquinimod 0.6 mg available for all subjects who completed the placebo-controlled MS-LAQ-302 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.

Study identification

NCT ID
NCT01047319
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
1,047 participants

Conditions and interventions

Interventions

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 27, 2010 (Actual)
Primary completion
Jun 30, 2017 (Actual)
Completion
Jun 30, 2017 (Actual)
Last update posted
Dec 9, 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 9, 2021 · Synced Oct 21, 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 public registry record, listed eligibility criteria, and available contact information for NCT01047319 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →