Brand Name | Status | Last Update |
---|---|---|
vpriv | Biologic Licensing Application | 2024-07-17 |
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
gaucher disease | Orphanet_355 | D005776 | E75.22 |
Code | Description |
---|---|
J3385 | Injection, velaglucerase alfa, 100 units |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Gaucher disease | D005776 | Orphanet_355 | E75.22 | 2 | 4 | 11 | 5 | 8 | 26 |
Disease | D004194 | EFO_0000408 | R69 | — | — | — | 1 | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Magnetic resonance imaging | D008279 | — | — | — | — | — | — | 1 | 1 |
Drug common name | Velaglucerase alfa |
INN | velaglucerase alfa |
Description | Velaglucerase alfa, sold under the brand name Vpriv and manufactured by Shire plc, is a hydrolytic lysosomal glucocerebroside-specific enzyme, which is a recombinant form of glucocerebrosidase indicated as a long-term enzyme replacement therapy for those suffering of Gaucher disease Type 1. It has an identical amino acid sequence to the naturally occurring enzyme. It was approved for use by the U.S. Food and Drug Administration (FDA) on February 26, 2010.
|
Classification | Enzyme |
Drug class | enzymes |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
PDB | 2WKL |
CAS-ID | — |
RxCUI | — |
ChEMBL ID | CHEMBL1201865 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB06720 |
UNII ID | 23HYE36B0I (ChemIDplus, GSRS) |