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Clinical Trial Summary

This was a Phase 4, open-label, single-arm, multicenter study to evaluate the efficacy and safety of dupilumab subcutaneous (SC) injection monotherapy in Japanese participants aged 18 or older with CRSwNP that is not adequately controlled with existing therapies. Duration of study period (per participant): - Screening Period (2 to 4 weeks) - Intervention Period (up to 52 weeks±3 days)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05049122
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date October 22, 2021
Completion date July 5, 2023

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