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Phase II Study Assessing Safety and Efficacy of APL-2 in Glomerulopathies

Lupus Nephritis Clinical Trial

Official title:
A Phase 2 Study to Evaluate the Safety and Biologic Activity of APL- 2 in Patients With IgA Nephropathy, Lupus Nephritis, Primary Membranous Nephropathy, or C3 Glomerulopathy (C3 Glomerulonephritis and Dense Deposit Disease)

Clinical Trial Summary

This is a Phase II trial assessing the safety and preliminary efficacy of daily APL-2 subcutaneous infusion administered for 16 weeks with a 6 month safety follow up, in patients with glomerulopathies

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03453619
Study type Interventional
Source Apellis Pharmaceuticals, Inc.
Contact
Status Active, not recruiting
Phase Phase 2
Start date January 22, 2018
Completion date December 2023
View Details
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