drugset / Trial / NCT03971422

A Study to Test Efficacy and Safety of Rozanolixizumab in Adult Patients With Generalized Myasthenia Gravis

NCT03971422 ↗

Phase 3 Completed 200 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the MycarinGstudy is to demonstrate the clinical efficacy and to assess safety and tolerability of rozanolixizumab in patients with generalized myasthenia gravis (MG).

Timeline

Start
2019-06-03
Primary completion
2021-08-31
Completion
2021-10-26

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Rozanolixizumab ~7 mg/kg; p <0.001; LS Mean Difference -2.586 (95% CI -4.091 to -1.249) NCT03971422 ↗

release “Positive topline results from UCB MycarinG study investigating the efficacy and safety of rozanolixizumab in patients with generalized myasthenia gravis (gMG) Study met primary” ucb.com ↗

release “The trial met its primary endpoint, demonstrating a statistically significant and clinically meaningful change from baseline” ucb.com ↗

release “pivotal Phase 3 MycarinG study in gMG, 2 which demonstrated that treatment with rozanolixizumab resulted in statistically significant” ucb.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Rozanolixizumab Monoclonal antibody 7 mg/kg Subcutaneous
Subject Rozanolixizumab Monoclonal antibody 10 mg/kg Subcutaneous