drugset / Trial / NCT03052751

Study to Test the Safety, Tolerability and Efficacy of UCB7665 in Subjects With Moderate to Severe Myasthenia Gravis

NCT03052751 ↗

Phase 2 Completed 43 enrolled UCB Biopharma S.P.R.L.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate the clinical efficacy of UCB7665 as a chronic-intermittent treatment in subjects with generalized myasthenia gravis (MG) who are classified as moderate to severe.

Timeline

Start
2017-05-15
Primary completion
2018-05-31
Completion
2018-08-06

Outcome

Missed primary endpoint

paper QMG (LS mean -1.8 vs -1.2, difference -0.7, 95% upper confidence limit [UCL] 0.8; p = 0.221; not statistically significant) PMID 33219142 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Rozanolixizumab Monoclonal antibody 4 mg/kg —
Subject Rozanolixizumab Monoclonal antibody 7 mg/kg —