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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-6587432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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