drugset / Trial / NCT06764160

Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Eculizumab in Chinese Adults With gMG

NCT06764160

Phase 3 Completed 15 enrolled Alexion Pharmaceuticals, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is an open-label, single-arm, multi-center study to evaluate the efficacy, safety, PK, PD, and immunogenicity of eculizumab in Chinese participants with refractory gMG. Approximately 15 participants will be enrolled in the study.

Timeline

Start
2025-01-06
Primary completion
2025-12-29
Completion
2025-12-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Eculizumab Monoclonal antibody Intravenous