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Not yet recruiting Phase 3 Interventional

A Study to Learn How Well People With Bronchiectasis Tolerate Continued Treatment With Verducatib After Earlier Studies (AIRTIVITY®-ON)

ClinicalTrials.gov ID: NCT07915219

Public ClinicalTrials.gov record NCT07915219. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 6, 2026, 7:10 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Roll-over Study Evaluating the Long-term Safety and Efficacy of an Oral Dose of Verducatib q.d. in Patients With Bronchiectasis (AIRTIVITY®-ON)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is for adults and adolescents who are at least 12 years old and have bronchiectasis. People can participate if they completed a previous study with the study medicine called verducatib. The purpose of this study is to find out how well verducatib is tolerated when people with bronchiectasis take it for a long time. The study also looks at breathing problems, how often lung flare-ups happen, and how quickly lung function changes. This is a roll-over study for participants who completed a previous study with verducatib: AIRTIVITY® (1397-0014) or CLAIRLEAF® (1397-0017). All participants receive verducatib. Participants take verducatib as tablets once a day at home. They may continue their usual treatment for bronchiectasis during the study. Participants can stay in the study for up to 1 year and 9 months. Treatment with verducatib can continue for up to 1 year and 6 months. About 6 study visits are done at the study site and about 4 are done by phone. At all visits, the doctors check participants' health and collect information on any health problems that occur during the study. The doctors also look at lung flare-ups and measure lung function over time.

Study identification

NCT ID
NCT07915219
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
1,500 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 11, 2027 (Estimated)
Primary completion
Jul 31, 2029 (Estimated)
Completion
Sep 10, 2029 (Estimated)
Last update posted
Nov 4, 2026

2027 – 2029

United States locations

U.S. sites
48
U.S. states
21
U.S. cities
43
Facility City State ZIP Site status
University of Arizona Tucson Arizona 85724 —
Newport Native MD, Inc Newport Beach California 92663 —
Paradigm Clinical Research - Redding Redding California 96001 —
University of California Davis Sacramento California 95817 —
National Jewish Health Denver Colorado 80206 —
Meris Clinical Research-Brandon-69466 Brandon Florida 33511 —
University of Florida College of Medicine Jacksonville Florida 32209 —
Mayo Clinic - Florida Jacksonville Florida 32224 —
Essence MD Research Naples Florida 34102 —
Vantage Clinical Trials - Tampa Tampa Florida 33614 —
Cleveland Clinic Florida Weston Florida 33331 —
Augusta University Augusta Georgia 30912 —
University of Kansas Medical Center Kansas City Kansas 66160 —
University of Michigan Ann Arbor Michigan 48109 —
Mayo Clinic, Rochester Rochester Minnesota 55905 —
HealthPartners Specialty Center 401 Building Saint Paul Minnesota 55130 —
Washington University School of Medicine St Louis Missouri 63110 —
University of Nebraska Medical Center Omaha Nebraska 68198-5910 —
New York Medical College - Hawthorne Hawthorne New York 10532 —
Northwell Health New Hyde Park New York 11040 —
New York University Langone Medical Center New York New York 10017 —
Icahn School of Medicine at Mount Sinai New York New York 10029 —
New York Presbyterian Hospital -Columbia University New York New York 10032 —
Stern Research Partners, LLC Huntersville North Carolina 28078 —
Pinehurst Medical Clinic, Inc. - East Pinehurst North Carolina 28374 —
University of Cincinnati Cincinnati Ohio 45267 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
Clinical Research Associates of Central PA DuBois Pennsylvania 15801 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Jefferson Health Honickman Center Philadelphia Pennsylvania 19107 —
Medical University of South Carolina Charleston South Carolina 29425 —
Clinical Research of Rock Hill Rock Hill South Carolina 29732 —
Horizon Clinical Research Group Cypress Texas 77429 —
Baylor University Medical Center Dallas Texas 75246 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
El Paso Pulmonary Association El Paso Texas 79902 —
University of Texas Medical Branch at Galveston Galveston Texas 77555 —
Baylor College of Medicine Houston Texas 77030 —
Metroplex Pulmonary & Sleep Center McKinney Texas 75069 —
IMA Clinical Research San Antonio San Antonio Texas 78229 —
University of Texas Health Science Center at Tyler Tyler Texas 75708 —
Intermountain Healthcare Murray Utah 84107-4107 —
University of Vermont Colchester Vermont 05446 —
Inova Fairfax Medical Campus Falls Church Virginia 22042 —
Virginia Commonwealth University Health Systems Richmond Virginia 23219 —
University of Washington Seattle Washington 98195 —
Providence Medical Research Center Spokane Washington 99204 —
University of Wisconsin Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 335 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07915219, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 4, 2026 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07915219 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →