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Study of Efficacy and Safety of AMG 334 in Adult Episodic Migraine Patients — EMPOwER  

Episodic Migraine Clinical Trial

Official title:
A 12-week Double-blind, Randomized, Multi-center Study Comparing the Efficacy and Safety of Once Monthly Subcutaneous AMG 334 Against Placebo in Adult Episodic Migraine Patients (EMPOwER)

Clinical Trial Summary

This study is to evaluate the efficacy and safety of AMG334 in adult patients with episodic migraine

Clinical Trial Description

This study used a single-cohort, 3-treatment arm, randomized, double-blind study design in adult patients with episodic migraine. The subjects were randomized to receive either erenumab or placebo in a 2:3:3 ratio (erenumab 140 mg: erenumab 70 mg: placebo). A screening period of 2 weeks was used to assess initial eligibility, followed by a 4-week baseline period. After randomization/Day 1, visits occurred at four week intervals until Week 12, which was the End of Treatment. The final visit, Last Patient Last Visit was a Safety Follow-Up visit, which occurred 12 weeks later, at Week 24. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03333109
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date February 8, 2018
Completion date January 13, 2020
View Details
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