MAS825
Sponsors
Novartis Pharma AG, Novartis Pharmaceuticals, The Hospital for Sick Children
Conditions
Atherosclerotic cardiovascular diseaseAutoinflammatory diseases including NLRC4-Gain of Function (GOF) also known as AIFEC (autoinflammation with infantile enterocolitis)COVID-19 Pneumonia, Impaired Respiratory FunctionClonal Hematopoiesis of Indeterminate Potential (CHIP)Coronary Heart DiseaseHealthy VolunteersHidradenitis SuppurativaNLRC4-GOF, AIFEC (Autoinflammation With Infantile Enterocolitis), XIAP Deficiency, CDC42 Mutations
Phase 1
Phase 2
Study of Efficacy and Safety of Investigational Treatments in Patients With Moderate to Severe Hidradenitis Suppurativa
Active, not recruitingNCT03827798
Start: 2019-02-27End: 2026-12-11Updated: 2026-02-06
Study of Efficacy and Safety of MAS825 in Patients With COVID-19
CompletedNCT04382651
Start: 2020-06-11End: 2021-04-21Updated: 2022-08-10
Study to Evaluate the Efficacy, Safety and Tolerability of MAS825 in Patients With Monogenic IL-18 Driven Autoinflammatory Diseases, Including NLRC4-GOF, XIAP Deficiency, or CDC42 Mutations
Active, not recruitingNCT04641442
Start: 2020-12-18End: 2032-04-07Updated: 2026-03-03
A Study to Investigate the Efficacy, Safety, and Tolerability of DFV890 and MAS825 for Inflammatory Marker Reduction in Adult Participants With Coronary Heart Disease and Clonal Hematopoiesis of Indeterminate Potential (CHIP)
CompletedNCT06097663
Start: 2024-02-15End: 2024-11-04Updated: 2026-03-27
A randomized, placebo-controlled, parallel-group, investigator- and participant-blinded Phase 2a study to investigate the efficacy, safety, and tolerability of DFV890 and MAS825 for inflammatory marker reduction in an adult population with coronary heart disease and Clonal Hematopoiesis of Indeterminate Potential (CHIP)
CompletedCTIS2023-506741-34-00
Start: 2024-02-16End: 2024-11-04Target: 16Updated: 2024-10-25
A three-period multicenter study, with a randomized-withdrawal, double-blinded, placebo-controlled design to evaluate the clinical efficacy, safety and tolerability of MAS825 in patients with monogenic IL-18 driven autoinflammatory diseases, including NLRC4-GOF, XIAP deficiency, or CDC42 mutations.
Active, not recruitingCTIS2023-504419-34-00
Start: 2021-04-29Target: 7Updated: 2025-11-07
A Phase II Trial to Evaluate the Clinical Efficacy, Safety and Tolerability of MAS825 in Pediatric and Adult Participants With Still's Disease
RecruitingNCT07203001
Start: 2025-11-03End: 2029-05-24Target: 20Updated: 2026-03-30
An open-label phase II trial to evaluate the clinical efficacy, safety and tolerability of MAS825 in pediatric and adult participants with Still’s disease
RecruitingCTIS2024-520208-25-00
Start: 2026-01-15Target: 15Updated: 2026-01-26