drugset / Trial / NCT04213274

Study of the Efficacy and Safety of RPH-104 in Adult Subjects With Schnitzler Syndrome

NCT04213274

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

EvaluationDrugModalityDoseRoute
Subject Goflikicept Monoclonal antibody 80 mg Subcutaneous

Indications