drugset / Trial / NCT05514873

An Open-label Study to Evaluate the Safety, Tolerability, and Efficacy of Subcutaneous Zilucoplan in Participants With Generalized Myasthenia Gravis Who Were Previously Receiving Intravenous Complement Component 5 Inhibitors

NCT05514873

Phase 3 Completed 26 enrolled UCB Biopharma SRL
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the safety and tolerability of switching from intravenous (IV) complement component 5 (C5) inhibitors to subcutaneous (SC) Zilucoplan in study participants with generalized myasthenia gravis (gMG)

Timeline

Start
2022-10-31
Primary completion
2024-03-13
Completion
2024-10-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Zilucoplan Peptide 0.3 mg/kg Subcutaneous