drugset / Trial / NCT03347188

A Study to Test if Fremanezumab Reduces Headache in Participants With Posttraumatic Headache (PTH)

NCT03347188

Phase 2 Completed 87 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the safety and efficacy of fremanezumab in adult participants aged 18 to 70 years, inclusive, for the prevention of PTH. The study will include a double-blind (DB) treatment period (12 weeks) and an open-label (OL) treatment period (12 weeks).

Timeline

Start
2017-12-18
Primary completion
2020-03-13
Completion
2020-06-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Fremanezumab Monoclonal antibody 675 mg Subcutaneous