drugset / Trial / NCT05878093
Dupilumab in Chinese Adult Participants With CRSwNP
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Dupilumab | Monoclonal antibody | 300 mg | Subcutaneous |
| Background | Budesonide | Small molecule | — | Intranasal |