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Clinical Trial Summary

Primary Objective: To assess the effect of dupilumab on sleep Secondary Objectives: - To evaluate the effect of dupilumab on additional patient reported sleep outcomes - To evaluate the effect of dupilumab on objective sleep assessment - To evaluate the effect of dupilumab on asthma symptoms - To evaluate the effect of dupilumab on lung function - To evaluate the safety of dupilumab


Clinical Trial Description

Study duration per participant will be approximately 16 weeks and up to 29 weeks including up to 5 weeks screening period, a 12-week treatment period and up to 12 weeks post-treatment follow-up period or until the participant switches to commercialized dupilumab (or other biologic product), whichever comes first. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04502862
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date August 10, 2020
Completion date November 10, 2023

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