Evidence map›Paper›PMID 34581002›Full record

Trial reportClinical and translational science2022

Dose-dependent inactivation of airway tryptase with a novel dissociating anti-tryptase antibody (MTPS9579A) in healthy participants: A randomized trial.

Sharon M Rymut, Siddharth Sukumaran, Gizette Sperinde, Meire Bremer, Joshua Galanter, Kenta Yoshida, Jordan Smith, Prajna Banerjee, Viyia Sverkos, Fang Cai and 6 more

Open access · goldAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Clinical and translational science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Review
  3. Emerging Therapies for Anaphylaxis.Immunology and allergy clinics of North America · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Target Therapies for Systemic Mastocytosis: An Update.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 3 countries.

Sharon M RymutDepartment of Clinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.
Siddharth SukumaranDepartment of Preclinical and Translational PKPD, Genentech, Inc., South San Francisco, California, USA.
Gizette SperindeDepartment of BioAnalytical Sciences, Genentech, Inc., South San Francisco, California, USA.
Meire BremerDepartment of Ophthalmology, Metabolism, Neurology, and Immunology Biomarker Development (OMNI-BD), Genentech, Inc., South San Francisco, California, USA.
Joshua GalanterDepartment of Safety Science, Genentech, Inc., South San Francisco, California, USA.
Kenta YoshidaDepartment of Clinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.
Jordan SmithDepartment of Biostatistics, F. Hoffmann-La Roche, Mississauga, Ontario, Canada.
Prajna BanerjeeOncology Biomarker Development, Genentech, Inc., South San Francisco, California, USA.
Viyia SverkosDepartment of BioAnalytical Sciences, Genentech, Inc., South San Francisco, California, USA.
Fang CaiDepartment of Ophthalmology, Metabolism, Neurology, and Immunology Biomarker Development (OMNI-BD), Genentech, Inc., South San Francisco, California, USA.
Verena SteffenDepartment of Biostatistics, Genentech, Inc., South San Francisco, California, USA.
Lindsay M HendersonDepartment of Clinical Pharmacology, Genentech, Inc., South San Francisco, California, USA.
Horace RheeEarly Clinical Development, Ophthalmology, Metabolism, Neurology, and Immunology (OMNI), Genentech, Inc., South San Francisco, California, USA.
Paula N BelloniEarly Clinical Development, Ophthalmology, Metabolism, Neurology, and Immunology (OMNI), Genentech, Inc., South San Francisco, California, USA.
Joseph H LinEarly Clinical Development, Ophthalmology, Metabolism, Neurology, and Immunology (OMNI), Genentech, Inc., South San Francisco, California, USA.
Tracy L StatonDepartment of Ophthalmology, Metabolism, Neurology, and Immunology Biomarker Development (OMNI-BD), Genentech, Inc., South San Francisco, California, USA.
Gene Therapy Laboratory · FRBiostatistical Consulting (United States) · USKaiser Permanente South San Francisco Medical Center · USRoche (Canada) · CA

Funding

Genentech, Inc.
6 · The paper itself

Abstract

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 (PKs), and systemic and airway pharmacodynamics (PDs) of MTPS9579A were assessed in healthy participants. In this phase I single-center, randomized, observer-blinded, and placebo-controlled study, single and multiple ascending doses of MTPS9579A were administered subcutaneously (s.c.) or intravenously (i.v.) in healthy participants. In addition to monitoring safety and tolerability, the concentrations of MTPS9579A, total tryptase, and active tryptase were quantified. This study included 106 healthy participants (82 on active treatment). Overall, MTPS9579A was well-tolerated with no serious or severe adverse events. Serum MTPS9579A showed a dose-proportional increase in maximum serum concentration (C

Indexed as

AsthmaArea Under CurveDose-Response Relationship, DrugDouble-Blind MethodHealthy VolunteersHumansTryptasesTryptases

Identifiers

PMID34581002
PMCPMC8841439
OpenAlexW3204108340

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.