A Prospective Observational Registry of Patients Treated With LUPKYNIS® (Voclosporin) in the US
NCT05337124 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 229
Last updated 2025-06-24
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).
Conditions
Interventions
- DRUG
-
LUPKYNIS
LUPKYNIS treatment per the approved US Prescribing Information
Sponsors & Collaborators
-
United BioSource, LLC
collaborator INDUSTRY -
Aurinia Pharmaceuticals Inc.
lead INDUSTRY
Principal Investigators
-
Aurinia Study Director · Aurinia Pharmaceuticals Inc.
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-04-05
- Primary Completion
- 2025-01-31
- Completion
- 2025-01-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
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