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Clinical Trial ● Currently Recruiting Phase II NCT06868290

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

Phase 2 Study Evaluating Rapcabtagene Autoleucel in Participants With Severe Active GPA or MPA — Recruiting • Phase II • Cardiology / Cardiovascular • NCT06868290.

📅 20 May 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT06868290
Sponsor
Novartis Pharmaceuticals
Start
2025-03-13
ClinicaliQ Trial Snapshot
  • Phase 2 Study Evaluating Rapcabtagene Autoleucel in Participants With Severe Active GPA or MPA — Recruiting • Phase II • Cardiology / Cardiovascular • NCT06868290.
  • Treatment being tested: Rapcabtagene autoleucel, a CAR-T cell therapy, is being evaluated against a comparator treatment in patients with severe active GPA or MPA—rare systemic vasculitides that cause significant organ damage and mortality if untreated.
  • Patient eligibility overview: The trial targets patients with documented severe active Granulomatosis with Polyangiitis or Microscopic Polyangiitis; specific inclusion/exclusion criteria would typically address disease activity markers, organ involvement, prior treatment history, and performance status.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

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)

Eligibility Snapshot
  • Key inclusion criteria: 1. Men and women, aged ≥18 and ≤ 75 years with a diagnosis of GPA or MPA according to the American College of Rheumatology/ European League Against Rheumatism 2022 (ACR/EULAR 2022) classification criteria 2. Positive test for ANCA-autoantibodies 3. GPA and MPA participants with severe active disease Key

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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