drugset / Trial / NCT02621931

Comparing Efficacy and Safety of 2 Dose Regimens of Subcutaneous Administration of TEV-48125 Versus Placebo for the Preventive Treatment of Chronic Migraine

NCT02621931 ↗

Phase 3 Completed 1130 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study is being conducted to evaluate two doses of TEV-48125 in adult patients with chronic migraine

Timeline

Start
2016-03-22
Primary completion
2017-04-11
Completion
2017-04-11

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Fremanezumab 675 mg/Placebo/Placebo; p <0.0001; LSM difference from placebo -1.8 (95% CI -2.46 to -1.15) NCT02621931 ↗

registry analysis (superiority test); Placebo vs Fremanezumab 675/225/225 mg; p <0.0001; LSM difference from placebo -2.1 (95% CI -2.76 to -1.45) NCT02621931 ↗

release “Chronic migraine study met all primary and secondary endpoints in both monthly and quarterly dosing regimens” tevapharm.com ↗

Publications

Drugs

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

Indications