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Completed Phase 3 Interventional Results available

Safety and Tolerability of Conversion From Oral, Injectable, or Infusion Disease Modifying Therapies to Dose-titrated Oral Siponimod (Mayzent) in Advancing RMS Patients

ClinicalTrials.gov ID: NCT03623243

Public ClinicalTrials.gov record NCT03623243. 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 19, 2026, 11:27 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

Exploring the Safety and Tolerability of Conversion From Oral, Injectable, or Infusion Disease Modifying Therapies to Dose-titrated Oral Siponimod (Mayzent) in Patients With Advancing Forms of Relapsing Multiple Sclerosis: A 6-month Open Label, Multi- Center Phase IIIb Study

Brief summary

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

To assess safety and tolerability of patients converting from approved Relapsing Multiple Sclerosis (RMS) Disease Modifying Therapies (DMTs) to siponimod.

Study identification

NCT ID
NCT03623243
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
185 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
Feb 14, 2019 (Actual)
Primary completion
Jul 6, 2022 (Actual)
Completion
Jul 6, 2022 (Actual)
Last update posted
Jun 20, 2024

2019 – 2022

United States locations

U.S. sites
54
U.S. states
23
U.S. cities
52
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35209 —
Novartis Investigative Site Cullman Alabama 35058 —
Alabama Neurology Associates Homewood Alabama 35209 —
Novartis Investigative Site Tucson Arizona 85718 —
Novartis Investigative Site Fresno California 93710 —
Novartis Investigative Site Fullerton California 92835 —
Novartis Investigative Site Irvine California 92617 —
Novartis Investigative Site Colorado Springs Colorado 80907 —
Novartis Investigative Site Denver Colorado 80209 —
Novartis Investigative Site Fort Collins Colorado 80528 —
Novartis Investigative Site Boca Raton Florida 33487 —
Novartis Investigative Site Bradenton Florida 34205 —
MS & Neuromuscular Center of Excellence Clearwater Florida 33761 —
Novartis Investigative Site Maitland Florida 32751 —
Novartis Investigative Site Miami Florida 33136 —
Novartis Investigative Site Ocala Florida 34471 —
Novartis Investigative Site Oldsmar Florida 34677 —
Novartis Investigative Site Orlando Florida 32806 —
Novartis Investigative Site Ormond Beach Florida 32174 —
Novartis Investigative Site Sarasota Florida 34243 —
Novartis Investigative Site Sunrise Florida 33351 —
Novartis Investigative Site Tampa Florida 33612 —
Novartis Investigative Site Vero Beach Florida 32960 —
Novartis Investigative Site Flossmoor Illinois 60422 —
Novartis Investigative Site Indianapolis Indiana 46256 —
Novartis Investigative Site Lexington Kentucky 40503 —
Novartis Investigative Site Lexington Kentucky 40509 —
Novartis Investigative Site Lexington Kentucky 40513 —
Novartis Investigative Site Rockville Maryland 20854 —
Novartis Investigative Site Clinton Township Michigan 48035 —
Novartis Investigative Site St Louis Missouri 63110 —
Novartis Investigative Site Las Vegas Nevada 89128 —
Novartis Investigative Site Hackensack New Jersey 07601 —
Novartis Investigative Site Asheville North Carolina 28806 —
Novartis Investigative Site Greensboro North Carolina 27405 —
Novartis Investigative Site Raleigh North Carolina 27607 —
Novartis Investigative Site Cincinnati Ohio 45219 —
Novartis Investigative Site Cleveland Ohio 44106-5028 —
Novartis Investigative Site Oklahoma City Oklahoma 73104 —
Abington Neurological Associates, Ltd Abington Pennsylvania 19001 —
Novartis Investigative Site Philadelphia Pennsylvania 19141 —
Novartis Investigative Site Willow Grove Pennsylvania 19090 —
Novartis Investigative Site Greer South Carolina 29650 —
Novartis Investigative Site Old Point Station South Carolina 29707 —
Novartis Investigative Site Cordova Tennessee 38018 —
Novartis Investigative Site Johnson City Tennessee 37604 —
Novartis Investigative Site Round Rock Texas 78681 —
Novartis Investigative Site San Antonio Texas 78258 —
Novartis Investigative Site Falls Church Virginia 22043 —
Novartis Investigative Site Kirkland Washington 98034 —
Novartis Investigative Site Seattle Washington 98122 —
Novartis Investigative Site Spokane Washington 99202 —
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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03623243, 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 20, 2024 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03623243 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →