Safety and Efficacy Study of Fingolimod in Taiwanese Adults (≥ 20years) With Relapsing Remitting Multiple Sclerosis

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age20-100
SponsorNovartis Pharmaceuticals

About this trial

The purpose of the study is to describe the safety profile of fingolimod in the Taiwanese multiple sclerosis population. This study aims to collect the safety data in patients newly initiated on fingolimod for one year.

Eligibility criteria

Qualifiers

None

Disqualifiers

Patients with the diagnosis of neuromyelitis optica.

Patients who are being treated with any investigational drug at the time of study entry.

In the last 6 months experienced myocardial infarction, unstable angina, stroke, transient ischemic attack, decompensated heart failure requiring hospitalization or Class III/IV heart failure

A history or presence of Mobitz Type II second-degree or third-degree atrioventricular block or sick sinus syndrome, unless patient has a functioning pacemaker

Trial design

Treatments tested in this trial

  • Fingolimod

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators