drugset / Trial / NCT03303079
Efficacy and Safety of Subcutaneous Administration of TEV-48125 for the Preventive Treatment of Chronic Migraine
RandomizedParallel-groupQuadruple-blindTreatment
Summary
To evaluate the efficacy and safety of subcutaneous (SC) administration of TEV-48125 \[monthly TEV-48125 225 mg (loading dose only: 675 mg) and TEV-48125 675 mg once over a period of 3 months\] compared with placebo for preventive treatment in Chronic Migraine patients
Timeline
- Start
- 2017-12-19
- Primary completion
- 2019-11-30
- Completion
- 2019-11-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fremanezumab | Monoclonal antibody | 225 mg | Subcutaneous |
| Subject | Fremanezumab | Monoclonal antibody | 675 mg | Subcutaneous |