drugset / Trial / NCT06015737

A Phase III Study to Investigate the Efficacy and Safety of Anifrolumab in Adults With Chronic and/or Subacute Cutaneous Lupus Erythematosus

NCT06015737

Phase 3 Active not recruiting 306 enrolled AstraZeneca Parexel · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

This study aims to evaluate the efficacy and safety of subcutaneous (SC) anifrolumab versus placebo in adult participants with chronic and/or subacute cutaneous lupus erythematosus (CLE).

Timeline

Start
2024-06-29
Primary completion
2026-12-11
Completion
2027-08-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Anifrolumab Monoclonal antibody Subcutaneous