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Terminated Phase 3 Interventional Results available

MS Study Evaluating Safety and Efficacy of Two Doses of Fingolimod Versus Copaxone

ClinicalTrials.gov ID: NCT01633112

Public ClinicalTrials.gov record NCT01633112. 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 27, 2026, 5:10 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 12-month, Randomized, Rater- and Dose-blinded Study to Compare the Efficacy and Safety of Fingolimod 0.25 mg and 0.5 mg Administered Orally Once Daily With Glatiramer Acetate 20 mg Administered Subcutaneously Once Daily in Patients With Relapsing-remitting Multiple Sclerosis

Brief summary

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

The purpose of this study was to demonstrate that at least one dose (0.5 mg followed by 0.25 mg) of fingolimod is superior to glatiramer acetate 20 mg SC in reducing the ARR up to 12 months in patients with relapsing-remitting MS

Study identification

NCT ID
NCT01633112
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
1,064 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 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
Aug 9, 2012 (Actual)
Primary completion
Apr 30, 2018 (Actual)
Completion
Apr 30, 2018 (Actual)
Last update posted
May 28, 2019

2012 – 2018

United States locations

U.S. sites
101
U.S. states
36
U.S. cities
91
Facility City State ZIP Site status
Novartis Investigative Site Cullman Alabama 35058 —
Novartis Investigative Site Phoenix Arizona 85004 —
Novartis Investigative Site Phoenix Arizona 85013 —
Novartis Investigative Site Phoenix Arizona 85018 —
Novartis Investigative Site Tucson Arizona 85741 —
Novartis Investigative Site Los Angeles California 90089 —
Novartis Investigative Site Sacramento California 95817 —
Novartis Investigative Site Aurora Colorado 80045 —
Novartis Investigative Site Boulder Colorado 80304 —
Novartis Investigative Site Denver Colorado 80220 —
Novartis Investigative Site Fort Collins Colorado 80528 —
Novartis Investigative Site Loveland Colorado 80538 —
Novartis Investigative Site Fairfield Connecticut 06824 —
Novartis Investigative Site Newark Delaware 19713 —
Novartis Investigative Site Washington D.C. District of Columbia 20007 —
Novartis Investigative Site Jacksonville Florida 32209 —
Novartis Investigative Site Maitland Florida 32751 —
Novartis Investigative Site Naples Florida 34119 —
Novartis Investigative Site New Port Richey Florida 34653 —
Novartis Investigative Site Orlando Florida 32806 —
Novartis Investigative Site Ormond Beach Florida 32174 —
Novartis Investigative Site Pompano Beach Florida 33060 —
Novartis Investigative Site Ponte Vedra Beach Florida 32082-4627 —
Novartis Investigative Site Port Charlotte Florida 33952 —
Novartis Investigative Site Sarasota Florida 34243 —
Novartis Investigative Site Tallahassee Florida 32308 —
Novartis Investigative Site Tampa Florida 33609 —
Novartis Investigative Site Vero Beach Florida 32960 —
Novartis Investigative Site West Palm Beach Florida 33407 —
Novartis Investigative Site Atlanta Georgia 30327 —
Novartis Investigative Site Elk Grove Village Illinois 60007 —
Novartis Investigative Site Evanston Illinois 60201 —
Novartis Investigative Site Flossmoor Illinois 60422 —
Novartis Investigative Site Northbrook Illinois 60062 —
Novartis Investigative Site Indianapolis Indiana 46202 —
Novartis Investigative Site Indianapolis Indiana 46256 —
Novartis Investigative Site West Des Moines Iowa 50314 —
Novartis Investigative Site Kansas City Kansas 66160 —
Novartis Investigative Site Lenexa Kansas 66212 —
Novartis Investigative Site Louisville Kentucky 40207 —
Novartis Investigative Site Hammond Louisiana 70403 —
Novartis Investigative Site New Orleans Louisiana 70121 —
Novartis Investigative Site Baltimore Maryland 21201 —
Novartis Investigative Site Boston Massachusetts 02215 —
Novartis Investigative Site Springfield Massachusetts 01104 —
Novartis Investigative Site Detroit Michigan 48201 —
Novartis Investigative Site Detroit Michigan 48202 —
Novartis Investigative Site Farmington Hills Michigan 48334 —
Novartis Investigative Site Grand Rapids Michigan 49503 —
Novartis Investigative Site Traverse City Michigan 49684-2340 —
Novartis Investigative Site Kansas City Missouri 64111 —
Novartis Investigative Site St Louis Missouri 63104 —
Novartis Investigative Site St Louis Missouri 63131 —
Novartis Investigative Site St Louis Missouri 63141 —
Novartis Investigative Site Great Falls Montana 59405 —
Novartis Investigative Site Las Vegas Nevada 89106 —
Novartis Investigative Site Freehold New Jersey 07728 —
Novartis Investigative Site Newark New Jersey 07103 —
Novartis Investigative Site Teaneck New Jersey 07666 —
Novartis Investigative Site Albuquerque New Mexico 87131 —
Novartis Investigative Site Albany New York 12208 —
Novartis Investigative Site Amherst New York 14226 —
Novartis Investigative Site Buffalo New York 14203 —
Novartis Investigative Site Patchogue New York 11772 —
Novartis Investigative Site Rochester New York 14642 —
Novartis Investigative Site Stony Brook New York 11794 —
Novartis Investigative Site Syracuse New York 13210 —
Novartis Investigative Site Chapel Hill North Carolina 27599-9500 —
Novartis Investigative Site Charlotte North Carolina 28204 —
Novartis Investigative Site Winston-Salem North Carolina 27157 —
Novartis Investigative Site Akron Ohio 44320 —
Novartis Investigative Site Bellevue Ohio 44811 —
Novartis Investigative Site Columbus Ohio 43210 —
Novartis Investigative Site Columbus Ohio 43221 —
Novartis Investigative Site Dayton Ohio 45408 —
Novartis Investigative Site Toledo Ohio 43614 —
Novartis Investigative Site Oklahoma City Oklahoma 73104 —
Novartis Investigative Site Oklahoma City Oklahoma 73112 —
Novartis Investigative Site Tulsa Oklahoma 74137 —
Novartis Investigative Site Portland Oregon 97225 —
Novartis Investigative Site Philadelphia Pennsylvania 19141 —
Novartis Investigative Site Spartanburg South Carolina 29302 —
Novartis Investigative Site Cordova Tennessee 38018 —
Novartis Investigative Site Knoxville Tennessee 37934 —
Novartis Investigative Site Nashville Tennessee 37204 —
Novartis Investigative Site Nashville Tennessee 37205 —
Novartis Investigative Site Dallas Texas 75214 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site Round Rock Texas 78681 —
Novartis Investigative Site San Antonio Texas 78258 —
Novartis Investigative Site Sherman Texas 75092 —
Novartis Investigative Site Salt Lake City Utah 84103 —
Novartis Investigative Site Alexandria Virginia 22310 —
Novartis Investigative Site Charlottesville Virginia 22903 —
Novartis Investigative Site Norfolk Virginia 23507 —
Novartis Investigative Site Richmond Virginia 23226 —
Novartis Investigative Site Roanoke Virginia 24018 —
Novartis Investigative Site Issaquah Washington 98029 —
Novartis Investigative Site Seattle Washington 98101 —
Novartis Investigative Site Seattle Washington 98122-4379 —
Novartis Investigative Site Milwaukee Wisconsin 53215 —

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 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01633112, 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 May 28, 2019 · Synced Oct 27, 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 NCT01633112 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →