Burosumab
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody | 
| Source | Human | 
| Target | FGF 23 | 
| Clinical data | |
| Pronunciation | bur OH sue mab | 
| Trade names | Crysvita | 
| Other names | KRN-23, KRN23, burosumab-twza | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a618034 | 
| License data | |
| Pregnancy category | 
 | 
| Routes of administration | Subcutaneous | 
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Elimination half-life | 16.4 days | 
| Identifiers | |
| CAS Number | |
| DrugBank | |
| ChemSpider | 
 | 
| UNII | |
| KEGG | |
| Chemical and physical data | |
| Formula | C6388H9904N1700O2006S46 | 
| Molar mass | 144090.15 g·mol−1 | 
Burosumab, sold under the brand name Crysvita, is a human monoclonal antibody medication approved 2018 for the treatment of X-linked hypophosphatemia and tumor-induced osteomalacia.