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
- Registry ID
- CMAS825D12201
- Source registry
- HEALTH_CANADA
- Status
- Ongoing
- Study type
- INTERVENTIONAL
- Sponsor
- NOVARTIS PHARMACEUTICALS CANADA INC
- Start date
- 2024-03-13
- Last update
- 2022-08-25
Conditions
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