A Study of Brenipatide (LY3537031) in Adult Participants With Moderate-to-Severe Chronic Obstructive Pulmonary Disease (COPD)

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age40-75
SponsorEli Lilly and Company

About this trial

The main purpose of this study is to assess if different dose levels of Brenipatide are safe and work the way they are intended to work in participants with moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD), when compared with placebo. The study will last approximately one year.

Eligibility criteria

Qualifiers

Current or former smokers with a smoking history of greater than or equal to (≥) 10 pack-years

Moderate-to-severe COPD (post-Bronchodilator (BD) Forced Expiratory Volume in 1 Second (FEV₁)/forced vital capacity (FVC) less than (<) 70 percent (%)

Modified Medical Research Council Dyspnea Scale (mMRC-DS) grade ≥2

Exacerbation history of ≥2 moderate or ≥1 severe exacerbations within the year prior to inclusion.

Disqualifiers

Have a known pre-existing, clinically important lung condition other than COPD.

Have a current or recent acute, active infection before screening and up to randomization.

Trial design

Treatments tested in this trial

  • Brenipatide
  • Placebo
  • Standard of Care

Treatment groups

606 Participants
are divided into 3 treatment groups

Sponsors and collaborators