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Completed Phase 3 Interventional Results available

Efficacy and Safety of Ofatumumab Compared to Teriflunomide in Patients With Relapsing Multiple Sclerosis.

ClinicalTrials.gov ID: NCT02792231

Public ClinicalTrials.gov record NCT02792231. 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 22, 2026, 4:37 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 Randomized, Double-blind, Double-dummy, Parallel-group Study Comparing the Efficacy and Safety of Ofatumumab Versus Teriflunomide in Patients With Relapsing Multiple Sclerosis.

Brief summary

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

To compare the efficacy and safety of ofatumumab administered subcutaneously (sc) every 4 weeks versus teriflunomide administered orally once daily in patients with relapsing multiple sclerosis

Study identification

NCT ID
NCT02792231
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
955 participants

Conditions and interventions

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
Aug 26, 2016 (Actual)
Primary completion
Jul 10, 2019 (Actual)
Completion
Oct 22, 2020 (Actual)
Last update posted
Nov 22, 2021

2016 – 2020

United States locations

U.S. sites
59
U.S. states
23
U.S. cities
54
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35233-0271 —
Novartis Investigative Site Cullman Alabama 35058 —
Novartis Investigative Site Tucson Arizona 85704 —
Novartis Investigative Site Aurora Colorado 80045 —
Novartis Investigative Site Basalt Colorado 81621 —
Novartis Investigative Site Boulder Colorado 80301 —
Novartis Investigative Site Centennial Colorado 80112 —
Novartis Investigative Site Colorado Springs Colorado 80907 —
Novartis Investigative Site Denver Colorado 80210 —
Novartis Investigative Site Fort Collins Colorado 80528 —
Novartis Investigative Site Fort Collins Colorado 907-280528 —
Novartis Investigative Site Fairfield Connecticut 06824 —
Novartis Investigative Site Newark Delaware 19713 —
Novartis Investigative Site Bradenton Florida 34205 —
Novartis Investigative Site Gainesville Florida 32611 —
Novartis Investigative Site Maitland Florida 32751 —
Novartis Investigative Site Ocala Florida 34471 —
Novartis Investigative Site Oldsmar Florida 34677 —
Novartis Investigative Site Ormond Beach Florida 32174 —
Novartis Investigative Site Palm Coast Florida 32164 —
Novartis Investigative Site Sarasota Florida 34243 —
Novartis Investigative Site St. Petersburg Florida 33713 —
Novartis Investigative Site Tallahassee Florida 32312 —
Novartis Investigative Site Tampa Florida 33603 —
Novartis Investigative Site Tampa Florida 33609 —
Novartis Investigative Site Tampa Florida 33612 —
Novartis Investigative Site Suwanee Georgia 30024 —
Novartis Investigative Site Anderson Indiana 46011 —
Novartis Investigative Site Indianapolis Indiana 46256 —
Novartis Investigative Site Wellesley Massachusetts 02481 —
Novartis Investigative Site Detroit Michigan 48202 —
Novartis Investigative Site Golden Valley Minnesota 55422 —
Novartis Investigative Site Billings Montana 59101 —
Novartis Investigative Site Great Falls Montana 59405 —
Novartis Investigative Site Albuquerque New Mexico 87131-0001 —
Novartis Investigative Site Asheville North Carolina 28806 —
Novartis Investigative Site Charlotte North Carolina 28202 —
Novartis Investigative Site Greensboro North Carolina 27405 —
Novartis Investigative Site Akron Ohio 44320 —
Novartis Investigative Site Columbus Ohio 43214 —
Novartis Investigative Site Columbus Ohio 43221 —
Novartis Investigative Site Westerville Ohio 43081 —
Novartis Investigative Site Portland Oregon 97225 —
Novartis Investigative Site Pittsburgh Pennsylvania 15212 —
Novartis Investigative Site Willow Grove Pennsylvania 19090 —
Novartis Investigative Site Greer South Carolina 29650 —
Novartis Investigative Site Cordova Tennessee 38018 —
Novartis Investigative Site Knoxville Tennessee 37922 —
Novartis Investigative Site Nashville Tennessee 37205 —
Novartis Investigative Site Greenville Texas 75401 —
Novartis Investigative Site Lubbock Texas 79410 —
Novartis Investigative Site Sherman Texas 75092 —
Novartis Investigative Site Orem Utah 84058 —
Novartis Investigative Site Salt Lake City Utah 84103 —
Novartis Investigative Site Salt Lake City Utah 84132 —
Novartis Investigative Site Kirkland Washington 98034 —
Novartis Investigative Site Seattle Washington 98122 —
Novartis Investigative Site Tacoma Washington 98405 —
Novartis Investigative Site Waukesha Wisconsin 53188 —

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 119 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02792231, 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 Nov 22, 2021 · Synced Oct 22, 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 NCT02792231 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →