Evidence map›Paper›PMID 41809869›Full record

ArticleERJ open research2026

Design and rationale of the AIR-NET trial: a randomised, open-label, multifactorial, multicentre, adaptive platform trial using a range of repurposed anti-inflammatory treatments to improve outcomes in patients with bronchiectasis within the EMBARC clinical research network.

Merete B Long, Jaa Ming New, Jamie Stobo, Margaret Band, Fiona McLaren-Neil, Rebecca Hull, Amy Gilmour, Holly Lind, Eve McIntosh, Rachel Galloway and 11 more

Abstract read
In one paragraph

Article in ERJ open research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Merete B LongDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Jaa Ming NewDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.ORCID https://orcid.org/0000-0002-1692-8204
Jamie StoboDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.ORCID https://orcid.org/0000-0003-4829-7440
Margaret BandTayside Clinical Trials Unit, University of Dundee, Dundee, UK.
Fiona McLaren-NeilTayside Clinical Trials Unit, University of Dundee, Dundee, UK.
Rebecca HullDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Amy GilmourDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Holly LindDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Eve McIntoshDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Rachel GallowayDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Zsofia EkeDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Bridget HarrisEMBARC/ELF Bronchiectasis Patient Advisory Group, Sheffield, UK.
Aran SinganayagamDepartment of Infectious Disease and National Heart and Lung Institute, Imperial College London, London, UK.
Anand ShahCentre of Bacterial Resistance Biology, Department of Infection, Imperial College London, London, UK.ORCID https://orcid.org/0000-0001-5257-520X
Jeffrey HuangDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.
Tom WilkinsonClinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Michael R LoebingerRoyal Brompton Hospital, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Charles S HaworthCambridge Centre for Lung Infection, Royal Papworth Hospital, Cambridge, UK.
Sanjay H ChotirmallLee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.ORCID https://orcid.org/0000-0003-0417-7607
Anthony De SoyzaPopulation and Health Science Institute, Newcastle University, Heaton, UK.ORCID https://orcid.org/0000-0002-8566-0344
James D ChalmersDivision of Respiratory Medicine and Gastroenterology, University of Dundee, Dundee, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neutrophilic airway inflammation is associated with disease severity and exacerbation frequency in bronchiectasis. Neutrophil protease inhibition significantly reduced exacerbation rates in phase II and III trials in bronchiectasis, highlighting this disease feature as an important therapeutic target. Additional neutrophil targeting therapeutics are needed to reduce the burden of the disease. Herein, we describe the protocol for the AIR-NET trial, the first randomised, open-label, multifactorial, multicentre, adaptive platform trial for people with bronchiectasis, run Methods and analysis: Participants with bronchiectasis confirmed by computed tomography, daily sputum production and evidence of active airway neutrophilic inflammation (based on a positive lateral flow test for neutrophil elastase (NE) activity), across 10 sites in the UK, will be randomised to one of several repurposed drugs with published evidence of effects on neutrophilic inflammation and acceptable safety profile (oral dose: disulfiram 400 mg once daily; dipyridamole 200 mg twice daily; doxycycline 100 mg once daily; n=42 per arm) or usual care, according to arm-specific eligibility criteria, and treated for 28 days. New arms will be added to the trial through an adaptive design. The primary end-point is change from baseline in sputum NE activity (a validated biomarker and surrogate of exacerbation risk) at day 28. Key secondary end-points include time-to-first exacerbation, quality of life questionnaires, neutrophil function and safety. Summary: AIR-NET will establish a multi-centre network with integrated clinical and translational capabilities for the investigation of therapies in bronchiectasis aiming to identify key anti-inflammatory mechanisms and effective re-purposed treatments.

Identifiers

PMID41809869
PMCPMC12969703

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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.