drugset / Trial / NCT03623243

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

NCT03623243

Phase 3 Completed 185 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

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

Timeline

Start
2019-02-14
Primary completion
2022-07-06
Completion
2022-07-06

Drugs

EvaluationDrugModalityDoseRoute
Subject BAF312 Unknown 2 mg Oral

Indications