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NCT06559150 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Non-cystic Fibrosis Bronchiectasis, sponsored by Verona Pharma.

Recruiting
Registry status
Phase 2
Development phase
180
Enrollment target
20
Study locations

NCT06559150: Recruiting Phase 2 study of Non-cystic Fibrosis Bronchiectasis, sponsored by Verona Pharma.

NCT06559150 is a Phase 2 study of Non-cystic Fibrosis Bronchiectasis that is actively recruiting participants, run by Verona Pharma. The registered enrollment target is 180 participants, above the 66-participant average among 3 other Non-cystic Fibrosis Bronchiectasis trials with a reported enrollment target (173% higher). The trial reports 20 study locations across 16 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06559150, a Phase 2 study of Non-cystic Fibrosis Bronchiectasis, is actively recruiting participants, sponsored by Verona Pharma.

RECRUITING
Registry status
Phase 2
Development phase
180 participants
Enrollment target
20
Study locations

Study Summary

This study is a randomized, double-blind, placebo-controlled study designed to assess the efficacy and safety of ensifentrine inhalation suspension (3 mg) delivered twice daily via standard jet nebulizer over at least 24 weeks, compared to placebo, in subjects with non-cystic fibrosis bronchiectasis (NCFBE).

Interventions

  • DRUG Nebulized Ensifentrine Suspension; 3 mg
  • DRUG Nebulized Placebo Solution

Study Locations (20)

North Carolina

  • University of North Carolina - Chapel Hill
  • Accellacare of Wilmington - Wilmington
  • Southeastern Research Center - Winston-Salem

California

  • So Cal Institute for Respiratory Diseases, Inc. - Los Angeles
  • University of California Davis Medical Center - Sacramento

Georgia

  • Emory University at Saint Joseph Pulmonary Clinic - Atlanta
  • Augusta University - Augusta

Alabama

  • Kirklin Clinic of UAB Hospital - Birmingham

Colorado

  • National Jewish Health Main Campus - Denver

District of Columbia

  • MedStar Georgetown University Hospital - Washington D.C.

Florida

  • University of Miami - Miami

Indiana

  • ASHA Clinical Research - Hammond

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2024-09-11
Est. Completion 2026-09
Phase Phase 2
Verona Pharma

7 total trials

What NCT06559150 shows while recruiting

NCT06559150 is an interventional study that assigns participants to a tested intervention. The registered 180 participants enrollment target is mid-sized for trials with a published cap, above the 66-participant average among 3 other Non-cystic Fibrosis Bronchiectasis trials with a reported enrollment target (173% higher).

The record links to 1 condition, with Non-cystic Fibrosis Bronchiectasis appearing as the primary indexed condition, and to 2 interventions - of which Nebulized Ensifentrine Suspension; 3 mg is the first listed.

NCT06559150 names 20 study sites across 16 states, led by North Carolina, California, Georgia.

Frequently Asked Questions

What is clinical trial NCT06559150 about?

NCT06559150 is a clinical study titled "A Phase II Study of Ensifentrine in Non-Cystic Fibrosis Bronchiectasis". This study is a randomized, double-blind, placebo-controlled study designed to assess the efficacy and safety of ensifentrine inhalation suspension (3 mg) delivered twice daily via standard jet nebulizer over at least 24 weeks, compared to placebo, in subjects with non-cystic fibrosis bronchiectasis...

What is the current status of trial NCT06559150?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 180 participants. The study started on 2024-09-11. Estimated completion is 2026-09.

What conditions does trial NCT06559150 study?

This clinical trial studies the following conditions: Non-cystic Fibrosis Bronchiectasis.

What interventions are being tested in trial NCT06559150?

The interventions under investigation include: Nebulized Ensifentrine Suspension; 3 mg (DRUG), Nebulized Placebo Solution (DRUG).

Who is sponsoring clinical trial NCT06559150?

This trial is sponsored by Verona Pharma, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06559150 being conducted?

This trial has 20 study locations across Alabama, California, Colorado, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06559150, the US trial registry maintained by the National Library of Medicine. NCT06559150 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.