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M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study

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 designe...

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Autores principales: Ling, Leona E., Hillson, Jan L., Tiessen, Renger G., Bosje, Tjerk, van Iersel, Mattheus Paulus, Nix, Darrell J., Markowitz, Lynn, Cilfone, Nicholas A., Duffner, Jay, Streisand, James B., Manning, Anthony M., Arroyo, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587432/
https://www.ncbi.nlm.nih.gov/pubmed/30402880
http://dx.doi.org/10.1002/cpt.1276
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author Ling, Leona E.
Hillson, Jan L.
Tiessen, Renger G.
Bosje, Tjerk
van Iersel, Mattheus Paulus
Nix, Darrell J.
Markowitz, Lynn
Cilfone, Nicholas A.
Duffner, Jay
Streisand, James B.
Manning, Anthony M.
Arroyo, Santiago
author_facet Ling, Leona E.
Hillson, Jan L.
Tiessen, Renger G.
Bosje, Tjerk
van Iersel, Mattheus Paulus
Nix, Darrell J.
Markowitz, Lynn
Cilfone, Nicholas A.
Duffner, Jay
Streisand, James B.
Manning, Anthony M.
Arroyo, Santiago
author_sort Ling, Leona E.
collection PubMed
description 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 ≈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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spelling pubmed-65874322019-07-02 M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study Ling, Leona E. Hillson, Jan L. Tiessen, Renger G. Bosje, Tjerk van Iersel, Mattheus Paulus Nix, Darrell J. Markowitz, Lynn Cilfone, Nicholas A. Duffner, Jay Streisand, James B. Manning, Anthony M. Arroyo, Santiago Clin Pharmacol Ther Research 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 ≈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. John Wiley and Sons Inc. 2018-12-04 2019-04 /pmc/articles/PMC6587432/ /pubmed/30402880 http://dx.doi.org/10.1002/cpt.1276 Text en © 2018 The Authors Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research
Ling, Leona E.
Hillson, Jan L.
Tiessen, Renger G.
Bosje, Tjerk
van Iersel, Mattheus Paulus
Nix, Darrell J.
Markowitz, Lynn
Cilfone, Nicholas A.
Duffner, Jay
Streisand, James B.
Manning, Anthony M.
Arroyo, Santiago
M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study
title M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study
title_full M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study
title_fullStr M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study
title_full_unstemmed M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study
title_short M281, an Anti‐FcRn Antibody: Pharmacodynamics, Pharmacokinetics, and Safety Across the Full Range of IgG Reduction in a First‐in‐Human Study
title_sort m281, an anti‐fcrn antibody: pharmacodynamics, pharmacokinetics, and safety across the full range of igg reduction in a first‐in‐human study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587432/
https://www.ncbi.nlm.nih.gov/pubmed/30402880
http://dx.doi.org/10.1002/cpt.1276
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