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nlrp3 inhibitor dfv890

Generic: NLRP3 Inhibitor DFV890

nlrp3 inhibitor dfv890: 4 clinical trials tracked.

nlrp3 inhibitor dfv890 evidence translation

What we can confirm

4 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about nlrp3 inhibitor dfv890, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 0 study sponsors

Related indications

Study sponsors

No additional listed-company sponsor is linked.

Clinical Trial Registry Records (4)

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)

NCT06097663Registry updated 2026-04-09·Phase 2
Completed

Primary endpoint: Ratio to Baseline Serum Levels of IL-6 for DFV890 Based on an Emax Model

InterventionalRandomizedquadruple31 enrolledStarted 2024-02Completion 2024-116 sites · Canada, Germany, United StatesNovartis Pharmaceuticals

A Randomized, Placebo-controlled, Parallel-group, Investigator- and Participant-blinded Phase 2a Study to Investigate the Efficacy, Safety, and Tolerability of DFV890 for Inflammatory Marker Reduction in Adult Participants With Coronary Heart Disease and Elevated hsCRP

NCT06031844Registry updated 2026-04-09·Phase 2
Completed

Primary endpoint: Ratio to Baseline Serum Levels of IL-6 for DFV890 Based on an Emax Model

InterventionalRandomizeddouble24 enrolledStarted 2023-10Completion 2024-127 sites · Canada, United StatesNovartis Pharmaceuticals

A Phase 1b, Open Label, Multi-center, Dose Optimization and Dose Expansion Study to Assess the Safety and Efficacy of DFV890 in Adult Patients With Myeloid Diseases

NCT05552469Registry updated 2026-09-10·Phase 1
Active, not recruiting

Primary endpoint: Incidence of Dose-limiting Toxicities (DLTs)

InterventionalRandomizedopen71 enrolledStarted 2023-05Completion 2027-0225 sites · France, Germany, Hong Kong, Italy…Novartis Pharmaceuticals

A Randomized, Two-arm, Placebo-controlled, Participant and Investigator-blinded Study Investigating the Efficacy, Safety and Tolerability of DFV890 in Patients With Symptomatic Knee Osteoarthritis

NCT04886258Registry updated 2026-03-31·Phase 2
Completed

Primary endpoint: Change From Baseline in Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain Subscale

InterventionalRandomizeddouble115 enrolledStarted 2021-09Completion 2024-1231 sites · Argentina, Czechia, Germany, Hungary…Novartis Pharmaceuticals