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A Study of 24 to 52 Weeks Treatment to Evaluate The Efficacy And Safety of Galvokimig in Study Participants With Moderate-to-Severe Chronic Obstructive Pulmonary Disease (COPD) With Chronic Bronchitis

NCT07725939

This study is recruiting at 7 US sites in 6 states, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of the study is to investigate the efficacy of galvokimig versus placebo in the time to the first acute exacerbation of chronic obstructive pulmonary disease (AECOPD) in study participants with moderate-to-severe COPD with chronic bronchitis.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Chronic Obstructive Pulmonary Disease With Chronic Bronchitis

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
40 to 80 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
UCB Biopharma SRL
Last updated on ClinicalTrials.gov
October 9, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Florida · 1

  • Copd01 50011 · Miami, FL

Georgia · 1

  • Copd01 50008 · Rincon, GA

Ohio · 1

  • Copd01 50003 · Columbus, OH

Pennsylvania · 1

  • Copd01 50002 · DuBois, PA

Texas · 2

  • Copd01 50001 · Boerne, TX
  • Copd01 50005 · Tomball, TX

Washington · 1

  • Copd01 50013 · Seattle, WA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.