Iptacopan in Patients With ANCA Associated Vasculitis
Condition(s) studied
Investigational drug(s) / intervention(s)
Iptacopan: LNP023 administered orally
Placebo: Matching placebo administered orally
Rituximab: Standard of care
Study summary
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.
Eligibility
Primary outcome measure(s)
- Sustained remission through Week 48 defined as complete remission at Week 24 without major relapse up to Week 48. — At Week 48
To assess the effect of iptacopan in achieving sustained remission compared to standard of care (SOC)
Trial sites (42)
| 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.
On this site
📄 Rituxan (rituximab) drug profile →More Novartis Pharmaceuticals trials in Spain
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 Spain