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

NCT07612878

This study is recruiting at 7 US sites in 5 states, according to its ClinicalTrials.gov record last updated .

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • COPD (Chronic Obstructive Pulmonary Disease)

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
40 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
Sanofi
Last updated on ClinicalTrials.gov
October 15, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Indiana · 1

  • IU Health Pulmonology & Critical Care Medicine · Indianapolis, IN

Kansas · 1

  • University of Kansas · Lawrence, KS

North Carolina · 1

  • Duke · Durham, NC

Ohio · 1

  • Ohio State University · Columbus, OH

Texas · 3

  • The Respire Institute · Houston, TX
  • Activian Clinical Research · Kingwood, TX
  • The Lung & Sleep Institute of North Texas · North Richland Hills, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.