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RECRUITING
NCT04480853
PHASE4

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

Sponsor: Novartis Pharmaceuticals

View on ClinicalTrials.gov

Summary

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.

Official title: A 12-month, Prospective, Multi-center Post-authorization Commitment (PAC) Study Monitoring Safety in Adult Patients With Relapsing-remitting Multiple Sclerosis Newly Initiated on Gilenya (Fingolimod) in Taiwan (SPRING)

Key Details

Gender

All

Age Range

20 Years - 100 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2020-10-12

Completion Date

2027-09-30

Last Updated

2026-04-06

Healthy Volunteers

No

Interventions

DRUG

Fingolimod

Fingolimod 0.5 mg QD, oral

Locations (6)

Novartis Investigative Site

Kaohsiung City, Taiwan

Novartis Investigative Site

Taichung, Taiwan

Novartis Investigative Site

Tainan, Taiwan

Novartis Investigative Site

Taipei, Taiwan

Novartis Investigative Site

Taipei, Taiwan

Novartis Investigative Site

Taoyuan District, Taiwan