drugset / Trial / NCT02025556

A Multicenter Assessment of LBR-101 in High Frequency Episodic Migraine

NCT02025556 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether monthly subcutaneous administration of LBR-101 (fremanezumab) is safe and provides migraine prevention in subjects with high frequency episodic migraine.

Timeline

Start
2014-01-31
Primary completion
2015-01-31
Completion
2015-03-31

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Low Dose; p < .0001; Mean Difference (Final Values) -2.81 (95% CI -4.07 to -1.55); Mixed Models Analysis NCT02025556 ↗

release “both doses of TEV-48125 met primary and secondary endpoints achieving significant reductions in mean monthly migraine days” tevapharm.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Fremanezumab Monoclonal antibody 225 mg Subcutaneous
Subject Fremanezumab Monoclonal antibody 675 mg Subcutaneous

Indications