AIRLEAF <sup>®</sup> –a study of verducatib as a new kind of treatment for bronchiectasis: a plain language summary

Plain Language Summary: What is this summary about? This plain language summary describes the key findings from a recent study of adults with a lung disease called bronchiectasis. What is bronchiectasis? Bronchiectasis is the third most common lung disease worldwide, and the number of people with the disease is growing. People with bronchiectasis have significantly reduced quality of life, and disease flare-ups in bronchiectasis (also known as exacerbations) are linked to an increased chance of the disease getting worse. What happened in the AIRLEAF<sup>®</sup> study? The AIRLEAF<sup>®</sup> study looked at a potential new bronchiectasis treatment called BI 1291583, which is now known as ‘verducatib’. In AIRLEAF<sup>®</sup>, 322 adults with bronchiectasis took part in the study. In order to be eligible to participate in the study, the adults who participated in AIRLEAF<sup>®</sup> had to have experienced at least two exacerbations that needed treatment with antibiotics in the year before they were enrolled in the study, or one exacerbation that needed treatment with antibiotics in the year before they were enrolled in the study as well as a high symptom burden. People were given either verducatib in one of three amounts (a low, medium, or high dose) or a placebo, taken as a pill (swallowed by mouth). A placebo looks like the study treatment but does not contain active ingredients. The study aimed to investigate the effectiveness and safety of verducatib when given to adults with bronchiectasis. The investigators also aimed to find out which dose of the study treatment would be most effective for people with bronchiectasis. What were the results? Researchers found that treatment with verducatib reduced the risk of people experiencing disease flare-ups, also known as exacerbations. People who took verducatib also had improved lung function, better quality of life, and spent less time on antibiotic treatment throughout the study period. The medium dose of verducatib was the most effective dose. Overall, the adverse events were similar between people who received verducatib and placebo. What do the results mean? The favorable results from the AIRLEAF<sup>®</sup> study mean that verducatib can be further investigated. A larger study called AIRTIVITY™, which is investigating the effectiveness and safety of verducatib in people with bronchiectasis, began in 2025. How to say (download PDF and double click sound icon to play sound)… Aeruginosa: ay-ruh-jih-noh-suh Bronchiectasis: bronk-ee-ek-tuh-sis Cathepsin: kuh-thep-sin Dipeptidyl peptidase: di-pep-tih-dul pep-tid-aze Protease: pro-tee-aze This is an abstract of the Plain Language Summary of Publication article. View the full Plain Language Summary PDF of this article to read the full-text Link to original article here Trial registration:ClinicalTrials.gov identifier: NCT05238675.

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Publication Details

Journal
Future Rare Diseases
Published
2025-12-08
DOI
https://doi.org/10.1080/23995270.2025.2580913
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
0.00

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article

AIRLEAF ® –a study of verducatib as a new kind of treatment for bronchiectasis: a plain language summary

Future Rare Diseases
Cystic Fibrosis Research Advances
article

AIRLEAF ® –a study of verducatib as a new kind of treatment for bronchiectasis: a plain language summary

article en

Abstract

Plain Language Summary: What is this summary about? This plain language summary describes the key findings from a recent study of adults with a lung disease called bronchiectasis. What is bronchiectasis? Bronchiectasis is the third most common lung disease worldwide, and the number of people with the disease is growing. People with bronchiectasis have significantly reduced quality of life, and disease flare-ups in bronchiectasis (also known as exacerbations) are linked to an increased chance of the disease getting worse. What happened in the AIRLEAF<sup>®</sup> study? The AIRLEAF<sup>®</sup> study looked at a potential new bronchiectasis treatment called BI 1291583, which is now known as ‘verducatib’. In AIRLEAF<sup>®</sup>, 322 adults with bronchiectasis took part in the study. In order to be eligible to participate in the study, the adults who participated in AIRLEAF<sup>®</sup> had to have experienced at least two exacerbations that needed treatment with antibiotics in the year before they were enrolled in the study, or one exacerbation that needed treatment with antibiotics in the year before they were enrolled in the study as well as a high symptom burden. People were given either verducatib in one of three amounts (a low, medium, or high dose) or a placebo, taken as a pill (swallowed by mouth). A placebo looks like the study treatment but does not contain active ingredients. The study aimed to investigate the effectiveness and safety of verducatib when given to adults with bronchiectasis. The investigators also aimed to find out which dose of the study treatment would be most effective for people with bronchiectasis. What were the results? Researchers found that treatment with verducatib reduced the risk of people experiencing disease flare-ups, also known as exacerbations. People who took verducatib also had improved lung function, better quality of life, and spent less time on antibiotic treatment throughout the study period. The medium dose of verducatib was the most effective dose. Overall, the adverse events were similar between people who received verducatib and placebo. What do the results mean? The favorable results from the AIRLEAF<sup>®</sup> study mean that verducatib can be further investigated. A larger study called AIRTIVITY™, which is investigating the effectiveness and safety of verducatib in people with bronchiectasis, began in 2025. How to say (download PDF and double click sound icon to play sound)… Aeruginosa: ay-ruh-jih-noh-suh Bronchiectasis: bronk-ee-ek-tuh-sis Cathepsin: kuh-thep-sin Dipeptidyl peptidase: di-pep-tih-dul pep-tid-aze Protease: pro-tee-aze This is an abstract of the Plain Language Summary of Publication article. View the full Plain Language Summary PDF of this article to read the full-text Link to original article here Trial registration:ClinicalTrials.gov identifier: NCT05238675.

Future Rare DiseasesVol. 5(1)
Goethe University Frankfurt (DE), Goethe-Institute United Kingdom (GB), University of California, Los Angeles (US), Nanyang Technological University (SG), University of Dundee (GB), Georgetown University (US), Keio University (JP), Georgetown University Medical Center (US), Cystic Fibrosis Foundation (US), Tan Tock Seng Hospital (SG), Boehringer Ingelheim (Taiwan) (TW), National Heart, Lung, and Blood Institute (US), Rappaport Family Institute for Research in the Medical Sciences (IL), German Centre for Cardiovascular Research (DE), German Center for Lung Research (DE), Boehringer Ingelheim (China) (CN), Boehringer Ingelheim (Australia) (AU), Charité - Universitätsmedizin Berlin (DE)
Pfizer, AstraZeneca, GlaxoSmithKline, Sanofi, Gilead Sciences, Chiesi Farmaceutici, CSL Behring, McGill University, Vertex Pharmaceuticals, Insmed, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Grifols, Genentech
Openalex Percentile: Top 31%
Cystic Fibrosis Research Advances
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