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Completed Phase 3 Interventional Results available

BRAVO Study: Laquinimod Double-blind Placebo-controlled Study in Participants With Relapsing-Remitting Multiple Sclerosis (RRMS) With a Rater Blinded Reference Arm of Interferon β-1a (Avonex®)

ClinicalTrials.gov ID: NCT00605215

Public ClinicalTrials.gov record NCT00605215. 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 25, 2026, 6:40 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, Randomized, Parallel-Group Study Performed in Subjects With Relapsing-Remitting Multiple Sclerosis (RRMS) to Assess the Efficacy, Safety and Tolerability of Laquinimod Over Placebo in a Double-blind Design and of a Reference Arm of Interferon β-1a (Avonex®) in a Rater-blinded Design

Study identification

NCT ID
NCT00605215
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
1,331 participants

Conditions and interventions

Interventions

  • Laquinimod Drug
  • Placebo Drug
  • Avonex® Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 55 Years
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
Apr 23, 2008
Primary completion
Jun 9, 2011
Completion
Jun 9, 2011
Last update posted
Apr 20, 2022

2008 – 2011

United States locations

U.S. sites
36
U.S. states
23
U.S. cities
34
Facility City State ZIP Site status
Teva Investigational Site 1267 Birmingham Alabama 35209
Teva Investigational Site 1237 Phoenix Arizona 85013
Teva Investigational Site 1252 Phoenix Arizona 85018
Teva Investigational Site 1279 Phoenix Arizona 85018
Teva Investigational Site 1276 Tucson Arizona 85741-3537
Teva Investigational Site 1272 Pasadena California 91105
Teva Investigational Site 1238 Sacramento California 95817
Teva Investigational Site 1280 Aurora Colorado 80045
Teva Investigational Site 1255 Orlando Florida 32806
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 1268 Lenexa Kansas 66214
Teva Investigational Site 1277 New Orleans Louisiana 70115
Teva Investigational Site 1263 Shreveport Louisiana 71103
Teva Investigational Site 1269 Baltimore Maryland 21201
Teva Investigational Site 1274 Grand Rapids Michigan 49525
Teva Investigational Site 1239 Lebanon New Hampshire 03766
Teva Investigational Site 1265 Teaneck New Jersey 07666
Teva Investigational Site 1273 Albany New York 12205
Teva Investigational Site 1264 Amherst New York 14226
Teva Investigational Site 1283 Cedarhurst New York 11516
Teva Investigational Site 1249 Raleigh North Carolina 27607
Teva Investigational Site 1262 Winston-Salem North Carolina 27103
Teva Investigational Site 1261 Akron Ohio 44320
Teva Investigational Site 1241 Canton Ohio 44718
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 1258 Philadelphia Pennsylvania 19107
Teva Investigational Site 1281 Nashville Tennessee 37205
Teva Investigational Site 1284 San Antonio Texas 78231
Teva Investigational Site 1248 Richmond Virginia 23298-0599
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 134 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00605215, 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 Apr 20, 2022 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00605215 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →