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

Publications

Drugs

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

Indications