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Completed Phase 3 Interventional Results available

Exploring the Efficacy and Safety of Siponimod in Patients With Secondary Progressive Multiple Sclerosis (EXPAND)

ClinicalTrials.gov ID: NCT01665144

Public ClinicalTrials.gov record NCT01665144. 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 25, 2026, 9:21 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 Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled Variable Treatment Duration Study Evaluating the Efficacy and Safety of Siponimod (BAF312) in Patients With Secondary Progressive Multiple Sclerosis Followed by Extended Treatment With Open-label BAF312.

Brief summary

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

Evaluate the safety and efficacy of Siponimod (BAF312) versus placebo in a variable treatment duration in patients with secondary progressive multiple sclerosis (Core Part) followed by extended treatment with open-label BAF312 to obtain data on long-term safety, tolerability and efficacy (Extension Part).

Study identification

NCT ID
NCT01665144
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
1,651 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 60 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
Dec 20, 2012 (Actual)
Primary completion
Apr 29, 2016 (Actual)
Completion
Mar 31, 2023 (Actual)
Last update posted
Jun 5, 2024

2012 – 2023

United States locations

U.S. sites
52
U.S. states
25
U.S. cities
48
Facility City State ZIP Site status
Novartis Investigative Site Phoenix Arizona 85032 —
Novartis Investigative Site Berkeley California 94705 —
Novartis Investigative Site Los Angeles California 90033 —
Novartis Investigative Site Oceanside California 92056 —
Novartis Investigative Site Sacramento California 95817 —
Novartis Investigative Site Aurora Colorado 80045 —
Novartis Investigative Site Basalt Colorado 81621 —
Novartis Investigative Site Boulder Colorado 80301 —
Novartis Investigative Site Colorado Springs Colorado 80907 —
Novartis Investigative Site Englewood Colorado 80113 —
Novartis Investigative Site Fairfield Connecticut 06824 —
Novartis Investigative Site Delray Beach Florida 33445 —
Novartis Investigative Site Hollywood Florida 33024 —
Novartis Investigative Site Jacksonville Florida 32209 —
Novartis Investigative Site Maitland Florida 32751 —
Novartis Investigative Site Ormond Beach Florida 32174 —
Novartis Investigative Site Port Charlotte Florida 33952 —
Novartis Investigative Site Tampa Florida 33609 —
Novartis Investigative Site Tampa Florida 33612 —
Novartis Investigative Site Vero Beach Florida 32960 —
Novartis Investigative Site Chicago Illinois 60612 —
Novartis Investigative Site Evanston Illinois 60201 —
Novartis Investigative Site Flossmoor Illinois 60422 —
Novartis Investigative Site Lenexa Kansas 66212 —
Novartis Investigative Site Baltimore Maryland 21287 —
Novartis Investigative Site Ann Arbor Michigan 48109 —
Novartis Investigative Site Detroit Michigan 48201 —
Novartis Investigative Site Detroit Michigan 48202 2689 —
Novartis Investigative Site Plymouth Minnesota 55446 —
Novartis Investigative Site St Louis Missouri 63131 —
Novartis Investigative Site Las Vegas Nevada 89106 —
Novartis Investigative Site Lebanon New Hampshire 03756 —
Novartis Investigative Site Freehold New Jersey 07728 —
Novartis Investigative Site Albuquerque New Mexico 87131-0001 —
Novartis Investigative Site New York New York 10017 —
Novartis Investigative Site New York New York 10029 —
Novartis Investigative Site Patchogue New York 11772 —
Novartis Investigative Site Stony Brook New York 11794 —
Novartis Investigative Site Charlotte North Carolina 28207 —
Novartis Investigative Site Akron Ohio 44320 —
Novartis Investigative Site Dayton Ohio 45408 —
Novartis Investigative Site Portland Oregon 97225 —
Novartis Investigative Site Springfield Oregon 97477 —
Novartis Investigative Site Philadelphia Pennsylvania 19104 —
Novartis Investigative Site Providence Rhode Island 02905 —
Novartis Investigative Site Dallas Texas 75216 —
Novartis Investigative Site Lubbock Texas 79410 —
Novartis Investigative Site San Antonio Texas 78258 —
Novartis Investigative Site Burlington Vermont 05401 —
Novartis Investigative Site Seattle Washington 98101 —
Novartis Investigative Site Seattle Washington 98122 —
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 238 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01665144, 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 Jun 5, 2024 · Synced Oct 25, 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 NCT01665144 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →