drugset / Trial / NCT03303105

Long-term Safety and Tolerability of Subcutaneous Administration of TEV-48125 for the Preventive Treatment of Migraine

NCT03303105

Phase 3 Completed 50 enrolled Otsuka Pharmaceutical Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the long-term safety and tolerability of subcutaneous (SC) administration of TEV-48125 (at 225 mg once monthly \[except for a loading dose of 675 mg for CM patients\] or at 675 mg every 3 months) for the preventive treatment of Chronic Migraine and Episodic Migraine patients

Timeline

Start
2017-12-07
Primary completion
2020-06-16
Completion
2020-06-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Fremanezumab Monoclonal antibody 225 mg Subcutaneous
Subject Fremanezumab Monoclonal antibody 675 mg Subcutaneous

Indications