drugset / Trial / NCT05878093

Dupilumab in Chinese Adult Participants With CRSwNP

NCT05878093

Phase 3 Completed 63 enrolled Sanofi
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a parallel group, Phase 3, 2-arm study for treatment. The purpose of this study is to evaluate dupilumab subcutaneous (SC) injections compared to placebo in Chinese adult participants with CRSwNP, on a background therapy with intranasal corticosteroids (budesonide nasal spray). Study details include: * The study duration will be up to 40 weeks. * The treatment duration will be up to 24 weeks. * The number of visits will be 7.

Timeline

Start
2023-05-16
Primary completion
2024-09-06
Completion
2024-11-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous
Background Budesonide Small molecule Intranasal