Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD) Characterized by an Eosinophilic Phenotype

A Phase 3 study evaluating lunsekimig versus placebo in adults with inadequately controlled COPD characterized by an eosinophilic phenotype.

Phase 3Phase
recruitingStatus
NCT07190209ClinicalTrials.gov

About the study

This Phase 3 study is evaluating lunsekimig, an investigational biologic, compared with placebo in adults with inadequately controlled COPD whose disease is characterized by an eosinophilic phenotype — a subtype linked to higher blood eosinophil counts. Participants attend study visits at our Madison Heights office over approximately one year.

Who can participate

You may be eligible if you:

  • Are between 40 and 80 years old
  • Have a diagnosis of COPD that remains inadequately controlled on current therapy
  • Have bloodwork suggesting an eosinophilic phenotype
  • Are willing to attend on-site visits over 52 weeks

A research coordinator will confirm eligibility at a screening visit.

What to expect

  • An initial screening visit including spirometry, bloodwork, and eligibility review
  • Regular follow-up visits with breathing tests and study drug administration
  • Compensation for time and travel at each visit
◈ This study is enrolling now

Think you might qualify?

A coordinator can tell you in one short phone call — or send us your details and we'll call you.