FSGS Clinical Trial - Acthar for Treatment of Post-transplant FSGS

Status Withdrawn

Clinical Trial Summary

This is an open label safety and feasibility trial using Acthar® in addition to center-specific standard therapy including plasma exchange, for treatment of post transplant recurrent FSGS and post transplant recurrent idiopathic membranous nephropathy. Subjects will receive Acthar® 40 units subcutaneously (SC) twice weekly for two weeks then 80 units SC twice weekly for 24 weeks.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02399462
Study type	Interventional
Source	University of North Carolina, Chapel Hill
Contact
Status	Withdrawn
Phase	Phase 4
Start date	March 2021
Completion date	July 31, 2021

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