A randomized, double blind, placebo-controlled study comparing the efficacy of dupilumab to standard of care (SOC) treatment following hospitalization for a COPD exacerbation

Registry ID
2025-524392-23-00
Source registry
CTIS
Status
Authorised
Phase
PHASE4
Study type
INTERVENTIONAL
Sponsor
Regeneron Pharmaceuticals Inc.
Enrollment
120
Last update
2026-08-14

Conditions

Primary outcomes

Time to first all-cause event (all-cause event may include non-elective hospital readmission, Emergency Department (ED)/urgent care visit, or death), Number of moderate or severe COPD exacerbations

Locations

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