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Study details
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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Lunsekimig
  • 2.Take Placebo
PhasePhase 3

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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