Last updated on December 2018

A Study to Evaluate the Efficacy and Safety of TEV-48125 (Fremanezumab) for the Prevention of Episodic Cluster Headache (ECH)


Brief description of study

This is a 13-week, multicenter, randomized, double-blind, double-dummy, placebo-controlled, parallel-group study to compare the efficacy and safety of 2 dose regimens of TEV-48125 (Fremanezumab) versus placebo in adult patients for the prevention of ECH.

Clinical Study Identifier: NCT02945046

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Teva U.S. Medical Information

Teva Investigational Site 13840
Tampa, FL United States
1.75miles
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Recruitment Status: Open


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