Velaglucerase alfa

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Velaglucerase alfa
Clinical data
Legal status
  • (Prescription only)
Routes of
administration
Infusion
Pharmacokinetic data
Bioavailability N/A
Biological half-life Plasma: 5–12 minutes (absorbed by macrophages)
Identifiers
ATC code A16AB10
ChemSpider none
UNII 23HYE36B0I N
ChEMBL CHEMBL1201865 N
Chemical data
Formula C2532H3850N672O711S16
Molar mass 55.5 kDa (unglycosylated)
 NYesY (what is this?)  (verify)

Velaglucerase alfa (trade name VPRIV), 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.[1] It was approved for use by the U.S. Food and Drug Administration (FDA) on February 26, 2010.[2]

Competitive products[edit]

Imiglucerase is Genzyme's version of recombinant glucocerebrosidase. It is marketed globally under the trade name of Cerezyme.

In addition, Protalix and Pfizer are working to bring taliglucerase alpha to market in the U.S. The FDA is due to rule on its approvability in February 2011. The companies are expected also to file for marketing authorization in Europe and around the world.

References[edit]