Evidence map›Paper›PMID 39872387›Full record

ArticleERJ open research2025

Brensocatib in patients with bronchiectasis: subgroup analyses from the WILLOW trial.

James D Chalmers, Michael R Loebinger, Ariel Teper, Pamela J McShane, Carlos Fernandez, Sebastian Fucile, Charles S Haworth, Melanie Lauterio, Roald van der Laan, Vivian H Shih and 1 more

Abstract read
In one paragraph

Article in ERJ open research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Inflammatory Phenotypes of Bronchiectasis.Journal of personalized medicine · 2025
    Review
  8. Review
  9. 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

11 authors.

James D ChalmersDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Michael R LoebingerRoyal Brompton Hospital and National Heart and Lung Institute, Imperial College, London, UK.
Ariel TeperInsmed Incorporated, Bridgewater, NJ, USA.
Pamela J McShaneUniversity of Texas Health Science Center at Tyler, Tyler, TX, USA.
Carlos FernandezInsmed Incorporated, Bridgewater, NJ, USA.
Sebastian FucileInsmed Incorporated, Bridgewater, NJ, USA.
Charles S HaworthRoyal Papworth Hospital and University of Cambridge, Cambridge, UK.
Melanie LauterioInsmed Incorporated, Bridgewater, NJ, USA.
Roald van der LaanInsmed B.V., Utrecht, The Netherlands.
Vivian H ShihInsmed Incorporated, Bridgewater, NJ, USA.
Mark L MeterskyUniversity of Connecticut School of Medicine, Farmington, CT, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Bronchiectasis is a chronic inflammatory airway disease. Brensocatib, an oral, reversible inhibitor of dipeptidyl peptidase 1 (DPP1), reduces pulmonary inflammation by preventing the activation of neutrophil serine proteases. In the phase II WILLOW trial, brensocatib prolonged time to first exacerbation in patients with bronchiectasis. In this Methods: Adults with bronchiectasis treated with brensocatib (10 or 25 mg) or placebo once daily were analysed by baseline Bronchiectasis Severity Index (BSI) score (≤4 (mild), 5-8 (moderate), or ≥9 (severe)), exacerbation history (2 or ≥3 in the previous year), blood eosinophil count (<300 cells per µL or ≥300 cells per µL), long-term macrolide use (≥6 months; no or yes) and Results: Treatment with brensocatib Discussion: Patients treated with brensocatib had a numerically longer time to first exacerbation and reduced annualised rate of exacerbation

Identifiers

PMID39872387
PMCPMC11770772

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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.