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NCT04645589

Evaluating the Safety of Myfortic (Mycophenolate Sodium) in Patients With Lupus Nephritis

Sponsor: Novartis Pharmaceuticals

View on ClinicalTrials.gov

Summary

This is an open-label, prospective, single-arm, observational study in patients with Lupus nephritis (LN) who newly (i.e.,for the first time) received treatment of Enteric-coated Mycophenolate Sodium (EC-MPS).

Official title: Evaluating the Safety of Myfortic (Mycophenolate Sodium) in Patients With Lupus Nephritis: a 12 Month, Single-arm, Observational Study in Taiwan Population

Key Details

Gender

All

Age Range

20 Years - 75 Years

Study Type

OBSERVATIONAL

Enrollment

69

Start Date

2021-03-16

Completion Date

2025-08-13

Last Updated

2026-06-26

Healthy Volunteers

No

Conditions

Interventions

DRUG

Myfortic

There is no treatment allocation. Patients administered Myfortic by prescription that have started before inclusion of the patient into the study were enrolled.

Locations (6)

Novartis Investigative Site

Kaohsiung City, Taiwan

Novartis Investigative Site

Keelung, Taiwan

Novartis Investigative Site

Taichung, Taiwan

Novartis Investigative Site

Taipei, Taiwan

Novartis Investigative Site

Taipei, Taiwan

Novartis Investigative Site

Taoyuan, Taiwan