Key Insights

Highlights

Success Rate

91% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

4.4%

2 terminated out of 45 trials

Success Rate

90.9%

+4.4% vs benchmark

Late-Stage Pipeline

18%

8 trials in Phase 3/4

Results Transparency

40%

8 of 20 completed with results

Key Signals

8 with results91% success

Data Visualizations

Phase Distribution

37Total
Not Applicable (9)
P 1 (7)
P 2 (13)
P 3 (4)
P 4 (4)

Trial Status

Completed20
Recruiting14
Not Yet Recruiting4
Unknown3
Terminated2
Active Not Recruiting1

Trial Success Rate

90.9%

Benchmark: 86.6%

Based on 20 completed trials

Clinical Trials (45)

Showing 20 of 20 trials
NCT07720375Phase 2RecruitingPrimary

A Study of 24 to 52 Weeks Treatment to Evaluate The Efficacy And Safety of Galvokimig in Adult Study Participants With Non-Cystic Fibrosis Bronchiectasis

NCT06559150Phase 2RecruitingPrimary

A Phase II Study of Ensifentrine in Non-Cystic Fibrosis Bronchiectasis

NCT06603246Phase 1RecruitingPrimary

A Study to Test the Safety and Effects of Inhaled GDC-6988 in Participants With Muco-obstructive Disease

NCT07547436Phase 2SuspendedPrimary

A Study to Access Activity and Safety With SAR445399 Compared With Placebo in Participants Aged 18 to 80 Years of Age With Non-Cystic Fibrosis Bronchiectasis

NCT07709494Phase 1Recruiting

A Phase 1a/1b Study to Investigate the Safety, Tolerability, Microbiological Response, and Pharmacokinetics of Inhaled Rev-56 in Adult Healthy Volunteers and Adult Non-cystic Fibrosis Bronchiectasis (NCFB) Patients With Chronic P. Aeruginosa

NCT07245407RecruitingPrimary

A Translational Study for Phenotyping and Endotyping Chinese Patients With NCFBE

NCT06487273Not ApplicableRecruitingPrimary

Long-term Evaluation of the SIMEOX Device at Home in Non-cystic Fibrosis Bronchiectasis

NCT07616375Phase 3RecruitingPrimary

A Study to Assess the Safety of HSK31858 in Participants With Non-Cystic Fibrosis Bronchiectasis

NCT07608328Phase 4Not Yet RecruitingPrimary

Azithromycin to Modify Bronchiectasis Exacerbation Risk

NCT07599969Recruiting

Bronchiectasis Phenotype Identification Model

NCT07599839Recruiting

BASE: Bronchiectasis Severity and Exacerbation Risk Study

NCT06663176Phase 1Active Not RecruitingPrimary

Nebulised RESP30X Nitric Oxide Formulations in NCFB Patients With Pseudomonas Aeruginosa (Pa)

NCT05743946Phase 4CompletedPrimary

Trikafta for Patients With Non-cystic Fibrosis Bronchiectasis

NCT07289464Phase 1RecruitingPrimary

A Clinical Study of RSS0343 in Healthy Subjects

NCT05860803Not ApplicableRecruitingPrimary

Breathing Training and Exercise Capacity in Non-CFB

NCT05616221Phase 2CompletedPrimary

Study to Evaluate the Safety, Phage Kinetics, and Efficacy of Inhaled AP-PA02 in Subjects With Non-Cystic Fibrosis Bronchiectasis and Chronic Pulmonary Pseudomonas Aeruginosa Infection

NCT04594369Phase 3CompletedPrimary

A Study to Assess the Efficacy, Safety, and Tolerability of Brensocatib in Participants With Non-Cystic Fibrosis Bronchiectasis

NCT07048262Phase 2RecruitingPrimary

Dose Range Finding, Efficacy, and Safety Study of Nebulized CSL787 in Adults With Non-cystic Fibrosis Bronchiectasis (NCFB)

NCT05344508UnknownPrimary

An Expanded Access Study to Assess Brensocatib for Participants With Non-Cystic Fibrosis Bronchiectasis

NCT06242795Phase 4Recruiting

Hypertonic Saline in NCFB

Scroll to load more

Research Network

Activity Timeline