drugset / Trial / NCT03957681

A Phase 3 Study of KHK4827 in Patients With Systemic Sclerosis

NCT03957681 ↗

Phase 3 Completed 100 enrolled Kyowa Kirin, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the efficacy and safety of KHK4827 in patients with systemic sclerosis who have moderate to severe skin thickening

Timeline

Start
2019-05-23
Primary completion
2020-10-16
Completion
2025-04-11

Outcome

Met primary endpoint

release “The primary endpoint of this study was the change from baseline in mRSS at Week 24. Significant decreases in mRSS were observed in brodalumab-treated arm” kyowakirin.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Brodalumab Monoclonal antibody 210 mg Subcutaneous

Indications