Overview

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

Status:
Completed
Trial end date:
2015-03-31
Target enrollment:
Participant gender:
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.
Phase:
Phase 2
Details
Lead Sponsor:
Teva Branded Pharmaceutical Products R&D, Inc.
Collaborator:
NCGS, Inc.
Treatments:
Antibodies, Monoclonal