drugset / Trial / NCT07463521

A Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Ocular Myasthenia Gravis

NCT07463521 ↗

Phase 3 Recruiting 120 enrolled UCB Biopharma SRL
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of the study is to demonstrate the efficacy, safety and tolerability of rozanolixizumab compared with placebo in the treatment of adult study participants with Ocular Myasthenia Gravis.

Timeline

Start
2026-05-27
Primary completion
2028-12-01
Completion
2029-01-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Rozanolixizumab Monoclonal antibody — Subcutaneous