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.
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.
Lanzhou University Second Hospital, Lanzhou, Gansu, China
The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China
Beijing Children's Hospital, Capital Medical University, Beijing, Beijing, China
Rabin Medical Center, Petah Tikva, Israel
Hospital Quironsalud Zaragoza, Zaragoza, Spain
Rambam Health Care Campus, Haifa, Israel
Baylor Research Institute, Dallas, Texas, United States
Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan
The Jikei University School of Medicine, Minato-ku, Tokyo, Japan
Chiba Children's Hospital, Chiba, Japan
Children's Hospitals and Clinics of Minnesota, Minneapolis, Minnesota, United States
Sinai Hospital of Baltimore, Baltimore, Maryland, United States
North Shore Hematology/Oncology - Manhasset, Manhasset, New York, United States
Shaare Zedek Medical Center, Jerusalem, Israel
Maria Sklodowska Curie Children's Hospital, Bucharest, Romania
Mother and Child Health Care Institute of Serbia, Belgrade, Serbia
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