drugset / Trial / NCT07215949

Zilucoplan for Severe gMG Exacerbations

NCT07215949

Phase 3 Recruiting 15 enrolled Miriam Freimer UCB Pharma · collab
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicenter, interventional phase 3b study in participants with AChR+ gMG and severe exacerbation that require hospitalization. Patients will receive subcutaneous zilucoplan injections daily for 12 weeks. Participation in the study will last for approximately 18 weeks.

Timeline

Start
2026-01-20
Primary completion
2027-12-01
Completion
2028-04-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Zilucoplan Peptide Subcutaneous