Iptacopan: LNP023 administered orally
Placebo: Matching placebo administered orally
Rituximab: Standard of care
The purpose of this study is to evaluate the efficacy and safety of iptacopan compared to standard of care (SOC) to induce and maintain remission in study participants with active granulomatosis with polyangiitis (GPA) or microscopic polyangiitis (MPA), when used in combination with rituximab (RTX) induction. The trial will also assess the impact of iptacopan on disease relapses, evolution of renal function and proteinuria, GC side effects, patients' immune status, and QoL.
| Facility | City | Region | Status |
|---|---|---|---|
| Arizona Arthritis and Rheumatology Research PLLC | Mesa | Arizona | |
| Mayo Clinic Rochester | Rochester | Minnesota | |
| Novartis Investigative Site | CABA | Buenos Aires | |
| Novartis Investigative Site | La Plata | Buenos Aires | |
| Novartis Investigative Site | CABA | Argentina | |
| Novartis Investigative Site | Concord | New South Wales | |
| Novartis Investigative Site | Clayton | Victoria | |
| Novartis Investigative Site | Innsbruck | Tyrol | |
| Novartis Investigative Site | Graz | Austria | |
| Novartis Investigative Site | Vienna | Austria | |
| Novartis Investigative Site | Leuven | Vlaams Brabant | |
| Novartis Investigative Site | Roeselare | West-Vlaanderen | |
| Novartis Investigative Site | London | Ontario | |
| Novartis Investigative Site | Fleurimont | Quebec | |
| Novartis Investigative Site | Montreal | Quebec | |
| Novartis Investigative Site | Montreal | Quebec | |
| Novartis Investigative Site | Québec | Quebec | |
| Novartis Investigative Site | Shijiazhuang | Hebei | |
| Novartis Investigative Site | Zhengzhou | Henan | |
| Novartis Investigative Site | Beijing | China | |
| Novartis Investigative Site | Prague | Czechia | |
| Novartis Investigative Site | Aarhus N | Denmark | |
| Novartis Investigative Site | Herlev | Denmark | |
| Novartis Investigative Site | Angers | France | |
| Novartis Investigative Site | Brest | France | |
| Novartis Investigative Site | Dijon | France | |
| Novartis Investigative Site | Marseille | France | |
| Novartis Investigative Site | Paris | France | |
| Novartis Investigative Site | Toulouse | France | |
| Novartis Investigative Site | Kirchheim unter Teck | Baden-Wurttemberg | |
| Novartis Investigative Site | Munich | Bavaria | |
| Novartis Investigative Site | Ludwigshafen | Germany | |
| Novartis Investigative Site | Berlin | Germany | |
| Novartis Investigative Site | Mainz | Germany | |
| Novartis Investigative Site | Budapest | Hungary | |
| Novartis Investigative Site | Szeged | Hungary | |
| Novartis Investigative Site | Plasencia | Caceres | |
| Novartis Investigative Site | Pamplona | Navarre | |
| Novartis Investigative Site | Madrid | Spain | |
| Novartis Investigative Site | Istanbul | Pendik |
+ 2 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06388941 on ClinicalTrials.gov ↗ ← All trials in the UK