drugset / Trial / NCT04530110

A Study to Test if Fremanezumab is Effective in Preventing Migraine in Children and Adolescents

NCT04530110

Phase 3 Completed 506 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of the study is to evaluate the long-term safety and tolerability of subcutaneous fremanezumab in the preventive treatment of migraine in pediatric participants 6 to 17 years of age (inclusive at enrollment in the pivotal study). Secondary objectives are to evaluate the efficacy of subcutaneous fremanezumab in pediatric participants with migraine and to evaluate the immunogenicity of fremanezumab and the impact of ADAs on clinical outcomes in pediatric participants exposed to fremanezumab. The total duration of the study is planned to be up to 84 months.

Timeline

Start
2020-09-16
Primary completion
2025-08-15
Completion
2025-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Fremanezumab Monoclonal antibody Subcutaneous

Indications