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Evaluating the Safety of Myfortic (Mycophenolate Sodium) in Patients With Lupus Nephritis
Sponsor: Novartis Pharmaceuticals
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
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