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Clinical Trials in the UK / NCT06388941
Active, not recruiting Phase 2

Iptacopan in Patients With ANCA Associated Vasculitis

NCT06388941 · tracked via the Priya Life Science UK tracker
Sponsor
Novartis Pharmaceuticals
Phase
Phase 2
Started
2024-08-05
Last updated
2026-08-20

Condition(s) studied

Anti-Neutrophil Cytoplasm Antibodies (ANCA) Associated Vasculitis

Investigational drug(s) / intervention(s)

IptacopanPlaceboRituximab

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

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Newly diagnosed or relapsed GPA and MPA (according to the 2022 ACR/EULAR classification criteria for GPA and MPA) requiring treatment with RTX and GC as per investigator's judgement. * BVAS assessment with ≥1 major item, or ≥3 minor items, or ≥2 renal items at Screening. * Positive antibody test for anti-proteinase 3 (PR3) or anti-myeloperoxidase (MPO) antibodies at Screening or with history of documented evidence of a positive antibody test. Exclusion Criteria: * Other systemic disease which constitutes the primary illness, including but not limited to: eosinophilic granulomatosis with polyangiitis (EGPA), moderate to severe systemic lupus erythematosus, IgA vasculitis (Purpura Schönlein-Henoch), rheumatoid vasculitis, Sjögren's syndrome, anti-glomerular basement membrane (GBM) disease, cryoglobulinemic vasculitis, autoimmune hemolytic anemia, autoimmune lymphoproliferative syndrome or mixed connective tissue disease. * Alveolar hemorrhage requiring invasive pulmonary ventilation support at Screening. * Severe kidney disease defined as estimated glomerular filtration rate (eGFR) \<15 mL/minute/1.73m2, or kidney failure defined as receiving renal replacement therapy such as hemo(dia)filtration, hemo-/peritoneal dialysis, or having received a kidney transplant. * Received plasma exchange/-pheresis within 12 weeks prior to Screening.

Primary outcome measure(s)

Trial sites (42)

FacilityCityRegionStatus
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 the UK

Official registry record

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