RecruitingNCT07612878

The Study of Chronic Obstructive Pulmonary Disease (COPD) Participants Treated With Dupilumab (STRIDE) Registry


Sponsor

Sanofi

Enrollment

350 participants

Start Date

Aug 6, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

The STRIDE Registry will evaluate the real-world effectiveness and safety of dupilumab in participants with COPD. The primary objective is to describe characteristics of participants newly initiated with dupilumab for COPD. Secondary objectives are to determine whether treatment with dupilumab reduces moderate and/or severe COPD exacerbations; to determine the impact of treatment on lung function in COPD participants; to determine whether treatment with dupilumab improves the quality of life in COPD participants; and to describe safety of dupilumab among COPD participants. The external control cohort will include participants with COPD from the National Patient-Centered Clinical Research Network (PCORnet) consortium who are not being treated with dupilumab. In addition, chest images will be collected and banked for future research projects and consented participants will perform home spirometry.


Eligibility

Min Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Cohort 1: Dupilumab and Cohort 2: usual care only for people with copd, chronic obstructive pulmonary disease. The study is currently recruiting participants at 3 locations. People eligible for this study include aged 40 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGCohort 1: Dupilumab

medicine already approved by the FDA

OTHERCohort 2: usual care only

Usual care that patients receive


Locations(3)

IU Health Pulmonology & Critical Care Medicine

Indianapolis, Indiana, United States

Duke

Durham, North Carolina, United States

The Lung & Sleep Institute of North Texas

North Richland Hills, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07612878


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