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A Prospective Observational Registry of Patients Treated With LUPKYNIS® (Voclosporin) in the US — ENLIGHT-LN  

Lupus Nephritis Clinical Trial

Official title:
A Prospective Observational Registry of Patients Treated With LUPKYNIS® (Voclosporin) in the US

Clinical Trial Summary

This registry is an observational study designed to assess the utilization and effectiveness of LUPKYNIS in adult patients with lupus nephritis (LN) in the United States (US).

Clinical Trial Description

This registry is an observational study designed to assess the utilization and effectiveness of LUPKYNIS in patients with lupus nephritis (LN) in the United States (US). This registry is intended to benefit and support interests of patients, clinicians, regulatory bodies, payers, and industry by obtaining longitudinal data on LUPKYNIS. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05337124
Study type Observational [Patient Registry]
Source Aurinia Pharmaceuticals Inc.
Contact Aurinia Study Director
Phone 1-480-720-0394
Email clinicaltrials@auriniapharma.com
Status Recruiting
Phase
Start date March 25, 2022
Completion date June 1, 2030
View Details
See also
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