# Brensocatib—Another Therapeutic “Window of Opportunity” for Patients with Bronchiectasis

**Authors:** Florin-Dumitru Mihălțan, Ruxandra Ulmeanu, Ancuța-Alina Constantin

PMC · DOI: 10.3390/jcm15031257 · Journal of Clinical Medicine · 2026-02-04

## TL;DR

Brensocatib is a new drug that reduces inflammation in bronchiectasis by targeting neutrophil proteases, improving patient outcomes and reducing exacerbations.

## Contribution

Brensocatib is the first FDA-approved therapy targeting DPP-1 to treat non-cystic fibrosis bronchiectasis.

## Key findings

- Brensocatib significantly reduces exacerbation frequency and prolongs time to first exacerbation.
- The drug lowers sputum neutrophil protease activity with a favorable safety profile.
- Benefits were observed across multiple patient subgroups and alongside standard treatments.

## Abstract

Introduction: Bronchiectasis is a chronic, heterogeneous airway disease characterised by irreversible bronchial dilatation, recurrent infections, and persistent inflammation, leading to progressive lung damage, frequent exacerbations, and impaired quality of life. Neutrophil-driven inflammation, largely mediated by excessive activity of neutrophil serine proteases such as neutrophil elastase, represents a central pathogenic mechanism and an important therapeutic target. Methods: Brensocatib, a first-in-class, selective, and reversible inhibitor of dipeptidyl peptidase-1 (DPP-1), prevents the activation of neutrophil serine proteases during neutrophil maturation in the bone marrow. By reducing downstream protease activity, brensocatib modulates aberrant neutrophilic inflammation without broadly suppressing immune function. Results: Clinical studies, including the Phase-2 WILLOW trial and the Phase-3 ASPEN trial, have demonstrated that brensocatib significantly reduces exacerbation frequency, prolongs time to first exacerbation, and lowers sputum neutrophil protease activity, with a favourable safety profile. Importantly, these benefits were observed across multiple patient subgroups and in addition to standard-of-care therapies. Conclusions: As the first FDA-approved (12 August 2025) mechanism-based therapy for non–cystic fibrosis bronchiectasis, brensocatib represents a paradigm shift toward targeted, precision treatment of neutrophil-mediated airway disease. Its clinical efficacy, biomarker-driven rationale, and potential to reduce antibiotic dependence highlight brensocatib as a cornerstone therapy in bronchiectasis management and a promising strategy for other neutrophil-driven inflammatory conditions.

## Linked entities

- **Chemicals:** brensocatib (PubChem CID 118253852)
- **Diseases:** bronchiectasis (MONDO:0004822), cystic fibrosis (MONDO:0009061)

## Full-text entities

- **Genes:** ELANE (elastase, neutrophil expressed) [NCBI Gene 1991] {aka ELA2, GE, HLE, HNE, NE, PMN-E}, CTSC (cathepsin C) [NCBI Gene 1075] {aka CPPI, DPP-I, DPP1, DPPI, HMS, JP}
- **Diseases:** infections (MESH:D007239), bronchial dilatation (MESH:D001982), Bronchiectasis (MESH:D001987), lung damage (MESH:D008171), inflammation (MESH:D007249), airway disease (MESH:D029424)
- **Chemicals:** Brensocatib (MESH:C000619932)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

86 references — full list in the complete paper: https://tomesphere.com/paper/PMC12898296/full.md

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Source: https://tomesphere.com/paper/PMC12898296