Skip to content
Study details
Enrolling now

Efficacy, Safety and Tolerability of Lunsekimig in Adults with COPD

Sanofi
NCT IDNCT07190222ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

942

Study length

about 4.4 years

Ages

40–80

Locations

51 sites in AZ, CA, CO +20

What this study is about

This trial is testing a treatment called lunsekimig compared to a placebo (inactive pill) in adults who have poorly controlled COPD. The goal is to see if lunsekimig helps improve symptoms and how safe it is.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Lunsekimig
  • 2.Take Placebo

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Secondary: Change from baseline in post-Bronchodilator Forced Expiratory Volume in 1 second (post-BD FEV1), Change from baseline in pre-Bronchodilator Forced Expiratory Volume in 1 second (pre-BD FEV1), Change from baseline in the Chronic airways assessment Test (CAAT) score, Change from baseline in the E-RS:COPD total score, Change from baseline in the SGRQ-C total score, Incidence of participants with TEAEs, including AESIs, and SAEs

Body systems

Respiratory