Overview

Safety, Efficacy, Pharmacokinetics, Pharmacodynamics of ACZ885 in Patients With NALP3 Mutations and Clinical Symptoms

Status:
Completed
Trial end date:
2008-07-01
Target enrollment:
Participant gender:
Summary
This study will investigate the clinical efficacy, safety, pharmacokinetics (PK) and pharmacodynamics (PD) of ACZ885, administered intravenously and subcutaneously to patients with NALP3 mutations whose clinical symptoms are either untreated or insufficiently treated and require medical intervention.
Phase:
Phase 2
Details
Lead Sponsor:
Novartis Pharmaceuticals