drugset / Trial / NCT04213274
Study of the Efficacy and Safety of RPH-104 in Adult Subjects With Schnitzler Syndrome
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary goal of the study is to assess the efficacy and safety of RPH-104 in subjects with Schnitzler Syndrome using Schnitzler Disease Activity Score (SDAS), which includes the Physician's Global Assessment (PGA) and the local laboratory C-reactive protein (CRP) result
Timeline
- Start
- 2023-05
- Primary completion
- 2023-08
- Completion
- 2024-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Goflikicept | Monoclonal antibody | 80 mg | Subcutaneous |