drugset / Trial / NCT01688739

Ascending Single Doses of Erenumab (AMG 334) in Healthy Adults and Migraine Patients

NCT01688739

Phase 1 Completed 61 enrolled Amgen
RandomizedSequentialQuadruple-blindPrevention

Summary

The primary purpose of this study is to determine whether erenumab is safe and well tolerated in healthy adults and migraine patients. As part of the secondary objectives, this study will be conducted to characterize the pharmacokinetic (PK) profile of erenumab after single subcutaneous (SC) or intravenous (IV) doses in healthy participants and migraine patients as well as to characterize the effect of erenumab on the capsaicin-induced increase in dermal blood flow after single SC or IV doses in healthy participants and migraine patients.

Timeline

Start
2012-03-13
Primary completion
2013-03-27
Completion
2013-03-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Erenumab Monoclonal antibody 1 mg Subcutaneous
Subject Erenumab Monoclonal antibody 7 mg Subcutaneous
Subject Erenumab Monoclonal antibody 21 mg Subcutaneous
Subject Erenumab Monoclonal antibody 70 mg Subcutaneous
Subject Erenumab Monoclonal antibody 140 mg Subcutaneous
Subject Erenumab Monoclonal antibody 210 mg Subcutaneous

Indications