COMPLETED

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

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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).

Official Title

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

Quick Facts

Study Start:2022-04-05
Study Completion:2025-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05337124

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Lupus nephritis (LN) confirmed by biopsy
  2. * Initiating or have initiated treatment with commercial LUPKYNIS as per US approved Prescribing Information (PI)
  3. * Written informed consent
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Principal Investigator

Aurinia Study Director
STUDY_DIRECTOR
Aurinia Pharmaceuticals Inc.

Study Locations (Sites)

Site 00-05
South Gate, California, 90280
United States

Collaborators and Investigators

Sponsor: Aurinia Pharmaceuticals Inc.

  • Aurinia Study Director, STUDY_DIRECTOR, Aurinia Pharmaceuticals Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-04-05
Study Completion Date2025-01-31

Study Record Updates

Study Start Date2022-04-05
Study Completion Date2025-01-31

Terms related to this study

Additional Relevant MeSH Terms

  • Lupus Nephritis