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Late Breaking Abstract - Dose-dependent inactivation of airway tryptase with a novel dissociating anti-Tryptase antibody (MTPS9579A) in healthy volunteers

Tracy Staton, Siddharth Sukumaran, Sharon Rymut, Gizette Sperinde, Meire Bremer, Verena Steffen, Prajna Banerjee, Fang Cai, Jordan Smith, Horace Rhee, Paula Belloni, Joseph Lin
European Respiratory Journal 2019 54: PA3707; DOI: 10.1183/13993003.congress-2019.PA3707
Tracy Staton
1Genentech, South San Francisco, United States of America
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  • For correspondence: statont@gene.com
Siddharth Sukumaran
1Genentech, South San Francisco, United States of America
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Sharon Rymut
1Genentech, South San Francisco, United States of America
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Gizette Sperinde
1Genentech, South San Francisco, United States of America
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Meire Bremer
1Genentech, South San Francisco, United States of America
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Verena Steffen
1Genentech, South San Francisco, United States of America
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Prajna Banerjee
1Genentech, South San Francisco, United States of America
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Fang Cai
1Genentech, South San Francisco, United States of America
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Jordan Smith
1Genentech, South San Francisco, United States of America
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Horace Rhee
1Genentech, South San Francisco, United States of America
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Paula Belloni
1Genentech, South San Francisco, United States of America
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Joseph Lin
1Genentech, South San Francisco, United States of America
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Abstract

Background: Tryptase is the most abundant secretory granule protein in human lung mast cells and plays an important role in asthma pathogenesis. MTPS9579A is a novel monoclonal antibody that selectively inhibits tryptase activity by dissociating active tetramers into inactive monomers. The safety, tolerability, pharmacokinetics (PK), and airway pharmacodynamics (PD) of MTPS9579A were assessed in healthy volunteers.

Methods: The Phase I studies were single-center, randomized, observer-blinded, and placebo-controlled. Single and multiple ascending doses of MTPS9579A were administered subcutaneously (SC) or intravenously (IV) in healthy volunteers. An activity based probe immunoassay was developed and used to specifically measure active tryptase in nasosorption (non-invasive sampling of nasal mucosal lining fluid).

Results: This study included 106 healthy volunteers (82 on active). Overall, MTPS9579A was well tolerated with adverse events being predominantly mild or moderate. There were no serious adverse events reported. MTPS9579A showed dose-proportional increase in Cmax values and a half-life of 30-34 days. Rapid and dose dependent reduction in nasosorption active tryptase was observed post-dose, confirming activity of MTPS9579A in the airway.

Conclusions: A novel immunoassay was used to demonstrate for the first time that an investigative antibody therapeutic (MTPS9579A) can inhibit tryptase activity in the upper airway. A favorable safety and tolerability profile supports further assessment of MTPS9579A in asthma. PKPD relationship may help inform future trials.

  • Asthma
  • Biomarkers
  • Pharmacology

Footnotes

Cite this article as: European Respiratory Journal 2019; 54: Suppl. 63, PA3707.

This is an ERS International Congress abstract. No full-text version is available. Further material to accompany this abstract may be available at www.ers-education.org (ERS member access only).

  • Copyright ©the authors 2019
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Late Breaking Abstract - Dose-dependent inactivation of airway tryptase with a novel dissociating anti-Tryptase antibody (MTPS9579A) in healthy volunteers
Tracy Staton, Siddharth Sukumaran, Sharon Rymut, Gizette Sperinde, Meire Bremer, Verena Steffen, Prajna Banerjee, Fang Cai, Jordan Smith, Horace Rhee, Paula Belloni, Joseph Lin
European Respiratory Journal Sep 2019, 54 (suppl 63) PA3707; DOI: 10.1183/13993003.congress-2019.PA3707

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Late Breaking Abstract - Dose-dependent inactivation of airway tryptase with a novel dissociating anti-Tryptase antibody (MTPS9579A) in healthy volunteers
Tracy Staton, Siddharth Sukumaran, Sharon Rymut, Gizette Sperinde, Meire Bremer, Verena Steffen, Prajna Banerjee, Fang Cai, Jordan Smith, Horace Rhee, Paula Belloni, Joseph Lin
European Respiratory Journal Sep 2019, 54 (suppl 63) PA3707; DOI: 10.1183/13993003.congress-2019.PA3707
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