TY - JOUR
T1 - AIRLEAF®–a study of verducatib as a new kind of treatment for bronchiectasis
T2 - a plain language summary
AU - Chalmers, James D.
AU - Shteinberg, Michal
AU - Mall, Marcus A.
AU - O’Donnell, Anne E.
AU - Watz, Henrik
AU - Gupta, Abhya
AU - Frahm, Edith
AU - Eleftheraki, Anastasia
AU - Rauch, Johanna
AU - Chotirmall, Sanjay H.
AU - Armstrong, April W.
AU - Eickholz, Peter
AU - Hasegawa, Naoki
AU - Sauter, Wiebke
AU - McShane, Pamela J.
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2025/12/8
Y1 - 2025/12/8
N2 - 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® study? The AIRLEAF® study looked at a potential new bronchiectasis treatment called BI 1291583, which is now known as ‘verducatib’. In AIRLEAF®, 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® 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® 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.
AB - 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® study? The AIRLEAF® study looked at a potential new bronchiectasis treatment called BI 1291583, which is now known as ‘verducatib’. In AIRLEAF®, 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® 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® 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.
KW - Disease mechanisms
KW - Pathophysiology
KW - Respiratory disorders
KW - Treatments
KW - Trial/study design
UR - https://www.scopus.com/pages/publications/105024222907
U2 - 10.1080/23995270.2025.2580913
DO - 10.1080/23995270.2025.2580913
M3 - Article
AN - SCOPUS:105024222907
VL - 5
JO - Future Rare Diseases
JF - Future Rare Diseases
IS - 1
M1 - 2580913
ER -