An Open Label Randomized Phase IV Study of the Safety and Efficacy of ACTHAR GEL in Patients with Membranous (Class V) Lupus Nephritis
A study for patients with Lupus Nephritis using ACTHAR GEL
Sponsor: Questcor Pharmaceuticals, Inc.
Enrolling: Male and Female Patients
IRB Number: AAAM4152
U.S. Govt. ID: NCT01926054
Contact: Wooin Ahn: 212-305-0320 / wa2197@cumc.columbia.edu
Additional Study Information: The purpose of this study is to determine if Acthar gel is a safe and effective therapy for patients with membranous (Class V) lupus nephritis. Class V lupus nephritis is associated with the development of chronic kidney disease and end-stage renal (kidney) disease, and there is no clear therapy for treatment. Currently used therapies arent completely effective in causing a decrease in symptoms of Class V lupus nephritis. In this study the safety of two different doses of Acthar gel and its ability to decrease the symptoms of Class V lupus nephritis will be assessed with the goal of determining whether Acthar gel is an effective and safe treatment for Class V lupus nephritis.
This study is closed
Investigator
Wooin Ahn, MD
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For more information, please contact:
Wooin Ahn
wa2197@cumc.columbia.edu
212-305-0320