M281, an Anti-FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety across the Full Range of IgG Reduction in a First-In-Human Study.

CLINICAL PHARMACOLOGY & THERAPEUTICS(2019)

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摘要
M281 is a fully human, anti-neonatal Fc receptor (FcRn) antibody that inhibits FcRn-mediated immunoglobulin G (IgG) recycling to decrease pathogenic IgG while preserving IgG production. A randomized, double-blind, placebo-controlled, first-in-human study with 50 normal healthy volunteers was designed to probe safety and the physiological maximum for reduction of IgG. Intravenous infusion of single ascending doses up to 60 mg/kg induced dose-dependent serum IgG reductions, which were similar across all IgG subclasses. Multiple weekly doses of 15 or 30 mg/kg achieved mean IgG reductions of approximate to 85% from baseline and maintained IgG reductions >= 75% from baseline for up to 24 days. M281 was well tolerated, with no serious or severe adverse events (AEs), few moderate AEs, and a low incidence of infection-related AEs similar to placebo treatment. The tolerability and consistency of M281 pharmacokinetics and pharmacodynamics support further evaluation of M281 in diseases mediated by pathogenic IgG.
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关键词
Drug development,healthy subjects,hematology,immunology,mechanism-based pharmacokinetics-pharmacodynamics,monoclonal antibodies,phase I,safety,translational pharmacokinetics-pharmacodynamics
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