A mechanistic PK/PD model to enable dose selection of the potent anti‐tryptase antibody (MTPS9579A) in patients with moderate‐to‐severe asthma

Bibliographic Details
Title: A mechanistic PK/PD model to enable dose selection of the potent anti‐tryptase antibody (MTPS9579A) in patients with moderate‐to‐severe asthma
Authors: Sharon M. Rymut, Lindsay M. Henderson, Victor Poon, Tracy L. Staton, Fang Cai, Siddharth Sukumaran, Horace Rhee, Ryan Owen, Saroja Ramanujan, Kenta Yoshida
Source: Clinical and Translational Science, Vol 16, Iss 4, Pp 694-703 (2023)
Publisher Information: Wiley, 2023.
Publication Year: 2023
Collection: LCC:Therapeutics. Pharmacology
LCC:Public aspects of medicine
Subject Terms: Therapeutics. Pharmacology, RM1-950, Public aspects of medicine, RA1-1270
More Details: Abstract Tryptase, a protease implicated in asthma pathology, is secreted from mast cells upon activation during an inflammatory allergic response. MTPS9579A is a novel monoclonal antibody that inhibits tryptase activity by irreversibly dissociating the active tetramer into inactive monomers. This study assessed the relationship between MTPS9579A concentrations in healthy subjects and tryptase levels in serum and nasal mucosal lining fluid from healthy subjects and patients with moderate‐to‐severe asthma. These data were used to develop a mechanistic pharmacokinetic/pharmacodynamic (PK/PD) model that quantitatively inter‐relates MTPS9579A exposure and inhibition of active tryptase in the airway of patients with asthma. From initial estimates of airway tryptase levels and drug partitioning, the PK/PD model predicted almost complete neutralization of active tryptase in the airway of patients with asthma with MTPS9579A doses of 900 mg and greater, administered intravenously (i.v.) once every 4 weeks (q4w). Suppression of active tryptase during an asthma exacerbation event was also evaluated using the model by simulating the administration of MTPS9579A during a 100‐fold increase in tryptase secretion in the local tissue. The PK/PD model predicted that 1800 mg MTPS9579A i.v. q4w results in 95.7% suppression of active tryptase at the steady‐state trough concentration. Understanding how the exposure‐response relationship of MTPS9579A in healthy subjects translates to patients with asthma is critical for future clinical studies assessing tryptase inhibition in the airway of patients with moderate‐to‐severe asthma.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1752-8062
1752-8054
Relation: https://doaj.org/toc/1752-8054; https://doaj.org/toc/1752-8062
DOI: 10.1111/cts.13483
Access URL: https://doaj.org/article/9f61ef52477747f58a911a9bf124e120
Accession Number: edsdoj.9f61ef52477747f58a911a9bf124e120
Database: Directory of Open Access Journals
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More Details
ISSN:17528062
17528054
DOI:10.1111/cts.13483
Published in:Clinical and Translational Science
Language:English