drugset / Trial / NCT05986162

Safety and Preliminary Clinical Activity of Itolizumab in Dermatomyositis

NCT05986162

Phase 1 Unknown 44 enrolled Biotech Pharmaceutical Co., Ltd.
RandomizedSequentialOpen-labelTreatment

Summary

To evaluate the safety, tolerability, PK, PD, and preliminary clinical activity of Itolizumab in subjects with Dermatomyositis.

Timeline

Start
2023-12-30
Primary completion
2025-05-03
Completion
2025-06-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Itolizumab Monoclonal antibody 25 mg Intravenous
Subject Itolizumab Monoclonal antibody 50 mg Intravenous
Subject Itolizumab Monoclonal antibody 100 mg Intravenous

Indications