Summary

Eligibility
for people ages 18-70 (full criteria)
Location
at UCLA
Dates
study started
completion around
Principal Investigator
by Mrinalini Sarkar, MD (ucla)

Description

Summary

The purpose of this study is to evaluate the efficacy and safety of IV antifrolumab in adult patients with Active Proliferative Lupus Nephritis

Official Title

A Multicentre Randomized Double-Blind Placebo Controlled Phase 3 Study to Evaluate the Efficacy and Safety of Anifrolumab in Adult Patients With Active Proliferative Lupus Nephritis

Details

This is a Phase 3, multicenter, multinational, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of anifrolumab versus placebo as added to SOC (consisting of MMF and glucocorticoids) in adults with active proliferative Class III or Class IV LN (both with or without concomitant Class V). The total study duration may be up to approximately 116 weeks, including the Screening and Follow-up. Approximately 360 participants will be randomized in a 1:1 ratio to receive anifrolumab or matching placebo throughout during the Treatment Period.

Keywords

Lupus Nephritis, Lupus Nephritis, anifrolumab, Systemic Lupus Erythematosus, intravenous, Nephritis, Anifrolumab

Eligibility

Locations

  • Research Site accepting new patients
    Los Angeles California 90095 United States
  • Research Site accepting new patients
    La Jolla California 92037 United States
  • Research Site accepting new patients
    Orange California 92868 United States
  • Research Site accepting new patients
    La Palma California 90623 United States

Lead Scientist at University of California Health

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
AstraZeneca
ID
NCT05138133
Phase
Phase 3 Lupus Research Study
Study Type
Interventional
Participants
Expecting 360 study participants
Last Updated