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

No results posted yet for this study

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05337124 on ClinicalTrials.gov