Taliglucerase alfa is the recombinant active form of the human lysosomal enzyme, β-glucocerebrosidase. It was approved in 2012 and is marketed under the name Elelyso for use in patients with type 1 Gaucher's disease.
For the treatment of adult Type 1 Gaucher disease.
Shaare Zedek Medical Center, Jerusalem, Israel
All India Institute of Medical Sciences, New Delhi, India
Gazi University, Ankara, Turkey
O&O Alpan LLC, Fairfax, Virginia, United States
Shaare Zedek Medical Center, Jerusalem, Israel
Shaare Zedek Medical Center, Jerusalem, Israel
Rambam Medical Center, Haifa, Israel
Shaare Zedek Medical Center, Jerusalem, Israel
Morningside Medi-Clinic, Morningside, South Africa
Instituto Privado de Hematologia E Investigacion Clinica (I.P.H.I.C), Barrio Asuncion, Paraguay
Instituto Privado de Hematologia E Investigacion Clinica (I.P.H.I.C), Barrio Sajonia Asunción, Paraguay
Shaare Zedek Medical Center, Jerusalem, Israel
Morningside Medi-Clinic, Morningside, South Africa
Sha'are Zedek Medical Center, Jerusalem, Israel
University Research Foundation for Lysosomal Storage Diseases, Inc., Coral Springs, Florida, United States
University of Colorado Denver, Aurora, Colorado, United States
Shaare Zedek Medical Center, Jerusalem, Israel
Royal Free Hospital, London, United Kingdom
Lysosomal Disorders Service, Addenbrookes Hospital NHS Trust, Cambridge, United Kingdom
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