Eptinezumab
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized |
| Target | CALCA, CALCB |
| Clinical data | |
| Trade names | Vyepti |
| Other names | ALD403, eptinezumab-jjmr |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a620022 |
| License data |
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| Pregnancy category |
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| Routes of administration | Intravenous |
| Drug class | Calcitonin gene-related peptide antagonist |
| ATC code | |
| Legal status | |
| Legal status | |
| Identifiers | |
| CAS Number | |
| DrugBank | |
| ChemSpider |
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| UNII | |
| KEGG | |
| Chemical and physical data | |
| Formula | C6352H9838N1694O1992S46 |
| Molar mass | 143283.20 g·mol−1 |
Eptinezumab, sold under the brand name Vyepti, is a medication used for the preventive treatment of migraine in adults. It is a monoclonal antibody that targets calcitonin gene-related peptides (CGRP) alpha and beta. It is administered by intravenous infusion.
Eptinezumab was approved for medical use in the United States in February 2020, and in the European Union in January 2022.