Pemivibart
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Human |
| Target | Spike protein of SARS-CoV-2 |
| Clinical data | |
| Trade names | Pemgarda |
| Other names | VYD222 |
| AHFS/Drugs.com | Monograph |
| License data |
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| Routes of administration | Intravenous |
| ATC code |
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| Legal status | |
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Pemivibart, sold under the brand name Pemgarda, is a monoclonal antibody medication authorized for the pre-exposure prophylaxis (prevention) of COVID‑19. Pemivibart was developed by Invivyd.
The US Food and Drug Administration (FDA) issued an emergency use authorization for pemivibart in March 2024.