drugset / Trial / NCT06868290

Phase 2 Study Evaluating Rapcabtagene Autoleucel in Participants With Severe Active GPA or MPA

NCT06868290

Phase 2 Recruiting 126 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of rapcabtagene autoleucel versus comparator in participants with severe active Granulomatosis with Polyangiitis (GPA) or Microscopic Polyangiitis (MPA)

Timeline

Start
2025-03-13
Primary completion
2029-06-07
Completion
2030-05-24

Drugs

EvaluationDrugModalityDoseRoute
Subject rapcabtagene autoleucel Cell therapy