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Taking peoplePhase 3

Testing BI 1291583 tablets for bronchiectasis in adults and teenagers

Tests whether BI 1291583 helps people with bronchiectasis who have flare-ups.

Key facts

Who runs it
Boehringer Ingelheim
Where
Astana and Karaganda, KazakhstanSee the 2 sitesAlso in 45 other countries, 469 sites
Trial code
Registry title
The AIRTIVITY™ Study: A Study to Find Out Whether BI 1291583 Helps People With Bronchiectasis
Status
Recruiting
Phase
Phase 3
People taking part
1,755 people, planned
Started
9 Jun 2025
Expected to end
20 Dec 2027
Type of study
Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
Treatments tested
  • BI 1291583
  • Placebo matching BI 1291583
Record updated
12 November 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for people aged 12 or older with bronchiectasis, a lung disease with widened airways, who have had flare-ups that needed antibiotics.

Age
12 years or older. Adolescents must weigh at least 35 kg (77 lb) at Visit 1.
Sex
All sexes can join.
Disease stage
Bronchiectasis seen on a CT scan and confirmed by a radiologist. Past scans must not be older than five years. In the 12 months before Visit 1, at least 2 flare-ups needing antibiotics. Or at least 1 flare-up plus an SGRQ Symptoms score of >40 (adults only), or high symptom burden in the doctor's view (adolescents only). Adults must be able to cough up sputum for a Pseudomonas aeruginosa test.
Earlier treatment
People must not have had a dipeptidyl peptidase-1 (DPP1) (Cathepsin C (CatC)) inhibitor before. People who only got placebo in such studies can join. People on long-term antibiotics or CFTR-MT must have had at least one flare-up since starting it.

Main reasons for not taking part

  • New immune system weakness (immunodeficiency) diagnosed within 1 year before randomisation
  • Allergic bronchopulmonary aspergillosis, tuberculosis or non-tuberculosis mycobacterial infection that is being treated or needs treatment
  • Cancer now or within 5 years before screening, except some treated in situ skin or cervix cancers
  • Moderate or severe liver disease (Child-Pugh B or C), or eGFR <30 mL/min at Visit 1
  • Major surgery within 6 weeks before randomisation or planned during the trial

The registry criteria, word for word

Show all 17 criteriaShow less

Who can take part

  • Male or female participants. Woman of childbearing potential (WOCBP) must be ready and able to use highly effective methods of birth control per International Council of Harmonisation (ICH) M3 (R2) that result in a low failure rate of less than 1 % per year when used consistently and correctly. A list of contraception methods meeting these criteria is provided in the participant information
  • Signed and dated written informed consent and assent, if applicable, prior to admission to the study, in accordance with GCP and local legislation
  • Age of participants when signing the informed consent/assent ≥12 years; -- Adolescents need to weigh at least 35 kg at Visit 1
  • Clinical history consistent with bronchiectasis (e.g. cough, chronic sputum production, recurrent respiratory infections) and investigator confirmed diagnosis of bronchiectasis by CT scan where bronchiectasis has been documented by a radiologist; Participants whose past CT scan image records are not available will undergo a chest CT scan during Screening. Historical scans must not be older than five years
  • Adult participants should be able to produce sputum for Pseudomonas aeruginosa assessment during the screening period
  • History of documented pulmonary exacerbations (assessed and recorded by the investigator) requiring antibiotic treatment. In the 12 months before Visit 1, participants must have had either:; at least 2 exacerbations, or; at least 1 exacerbation and an St. George's Respiratory Questionnaire (SGRQ) Symptoms score of >40 at screening Visit 1 (adults only); at least 1 exacerbation and high symptom burden according to the investigator's judgement (adolescents only) For participants on oral or inhaled antibiotics as chronic treatment for bronchiectasis and participants on Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapy (CFTR-MT), at least one exacerbation must have occurred since initiation of antibiotics or CFTR-MT

Who cannot take part

  • Any clinically relevant (at the discretion of the investigator) acute respiratory infection or ongoing pulmonary exacerbation at screening visit or during the screening unless recovered in the opinion of the investigator prior to Visit 2
  • Major surgery (major according to the investigator's assessment) performed within 6 weeks prior to randomisation or scheduled during trial period
  • Previous treatment with a dipeptidyl peptidase-1 (DPP1) (Cathepsin C (CatC)) inhibitor. (Note: Participants that were randomised and only received placebo in studies with DPP1 (CatC) inhibitor are allowed.) Further exclusion criteria apply
  • Any new or newly diagnosed condition of primary or secondary immunodeficiency within 1 year before randomisation
  • Allergic bronchopulmonary aspergillosis being treated or requiring treatment
  • Tuberculosis or non-tuberculosis mycobacterial infection being treated or requiring treatment
  • Any relevant pulmonary, gastrointestinal, hepatic, renal, cardiovascular, metabolic, immunological, hormonal, or other disorder that, in the opinion of the investigator, may put the participant at risk by participating in the study
  • Any documented active or suspected malignancy or history of malignancy within 5 years prior to screening, except appropriately treated in situ non-melanoma skin cancers or in situ carcinoma of uterine cervix
  • Evidence or medical history of moderate or severe liver disease (Child-Pugh score B or C hepatic impairment)
  • Any findings in the medical examination and/or laboratory value assessed at Screening Visit 1 or during screening period, that in the opinion of the investigator may put the participant at risk by participating in the trial
  • estimated Glomerular Filtration Rate (eGFR) according to Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula (adults) or Chronic Kidney Disease Under 25 (CKiD-U25) (adolescents) <30 mL/min at Visit 1

Where in Kazakhstan

Also in 45 other countries, 469 sites

  • Multidisciplinary City Hospital №1 of the Akimat of AstanaAstana, KazakhstanContact: Boehringer IngelheimNo longer taking part
  • Regional Clinical Hospital of the Health Department of the Karaganda RegionKaraganda, KazakhstanContact: Boehringer IngelheimNo longer taking part

About the trial

What the trial wants to find out

This study is open to adults and adolescents aged 12 to under 18 with bronchiectasis. People can participate in this study if they produce sputum and have had flare-ups (also called exacerbations).

Read full original descriptionShow less

The purpose of this study is to find out whether a medicine called BI 1291583 helps people with bronchiectasis. Participants are put into 2 groups randomly, which means by chance. One group takes BI 1291583 tablets and the other group takes placebo tablets. A placebo tablet looks like the BI 1291583 tablet but does not contain any medicine. Participants take 1 tablet once a day for up to 1 year and 6 months.

Participants are in the study for up to 1 year and 8 months. During this time, participants visit the study site up to 10 times and get about 13 phone calls from the site staff. Participants regularly complete a diary on a smartphone about their bronchiectasis symptoms and study doctors regularly check for any changes. The study doctors document when participants experience flare-ups. The number of flare-ups is compared between the participants who receive BI 1291583 and those who receive the placebo. The study doctors also regularly check participants' health and take note of any unwanted effects.

The 2 groups in the trial

  • Treatment armTreatment being tested

    Treatment: BI 1291583

  • Placebo armPlacebo, for comparison

    Treatment: Placebo matching BI 1291583

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
Official title
A Phase III, Randomised, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of BI 1291583 2.5 mg Administered Once Daily for up to 76 Weeks in Patients With Bronchiectasis (The AIRTIVITY™ Study)
Plain-language title
Testing BI 1291583 tablets for bronchiectasis in adults and teenagersGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 14 November 2026.
Publications
Record updated
12 November 2026