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Velaglucerase alfa

Generic Name
Velaglucerase alfa
Brand Names
Vpriv
Drug Type
Biotech
CAS Number
884604-91-5
Unique Ingredient Identifier
23HYE36B0I

Overview

Velaglucerase alfa is a gene-activated human recombinant glucocerebrosidase used for the treatment of Type 1 Gaucher disease, caused by a deficiency of the lysosomal enzyme glucocerebrosidase. Additionally, Velaglucerase alfa has also been investigated for use in Type 3 Gaucher disease.

Background

Velaglucerase alfa is a gene-activated human recombinant glucocerebrosidase used for the treatment of Type 1 Gaucher disease, caused by a deficiency of the lysosomal enzyme glucocerebrosidase. Additionally, Velaglucerase alfa has also been investigated for use in Type 3 Gaucher disease.

Indication

Velaglucerase alfa is a hydrolytic lysosomal glucocerebroside-specific enzyme indicated for long-term enzyme replacement therapy for pediatric and adult patients with type 1 Gaucher disease.

Associated Conditions

  • Gaucher Disease, Type 1

FDA Approved Products

VPRIV
Manufacturer:Takeda Pharmaceuticals America, Inc.
Route:INTRAVENOUS
Strength:2.5 mg in 1 mL
Approved: 2021/09/30
NDC:54092-701

Singapore Approved Products

VPRIV POWDER FOR SOLUTION FOR INFUSION 400 UNITS/VIAL
Manufacturer:Vetter Pharma-Fertigung GmbH & Co. KG (bulk production and primary packager), Cangene bioPharma LLC (bulk production and primary packager)
Form:INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Strength:10 mg/vial
Online:Yes
Approved: 2021/02/24
Approval:SIN16107P

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