TY - JOUR
T1 - Systemic safety of bevacizumab versus ranibizumab for neovascular age-related macular degeneration
AU - Moja, Lorenzo
AU - Lucenteforte, Ersilia
AU - Kwag, Koren H
AU - Bertele, Vittorio
AU - Campomori, Annalisa
AU - Chakravarthy, Usha
AU - D'Amico, Roberto
AU - Dickersin, Kay
AU - Kodjikian, Laurent
AU - Lindsley, Kristina
AU - Loke, Yoon
AU - Maguire, Maureen
AU - Martin, Daniel F
AU - Mugelli, Alessandro
AU - Mühlbauer, Bernd
AU - Püntmann, Isabel
AU - Reeves, Barnaby
AU - Rogers, Chris
AU - Schmucker, Christine
AU - Subramanian, Manju L
AU - Virgili, Gianni
PY - 2014
Y1 - 2014
N2 - Neovascular age-related macular degeneration (AMD) is the leading cause of legal blindness in elderly populations of industrialised countries. Bevacizumab (Avastin®) and ranibizumab (Lucentis®) are targeted biological drugs (a monoclonal antibody) that inhibit vascular endothelial growth factor, an angiogenic cytokine that promotes vascular leakage and growth, thereby preventing its pathological angiogenesis. Ranibizumab is approved for intravitreal use to treat neovascular AMD, while bevacizumab is approved for intravenous use as a cancer therapy. However, due to the biological similarity of the two drugs, bevacizumab is widely used off-label to treat neovascular AMD.
AB - Neovascular age-related macular degeneration (AMD) is the leading cause of legal blindness in elderly populations of industrialised countries. Bevacizumab (Avastin®) and ranibizumab (Lucentis®) are targeted biological drugs (a monoclonal antibody) that inhibit vascular endothelial growth factor, an angiogenic cytokine that promotes vascular leakage and growth, thereby preventing its pathological angiogenesis. Ranibizumab is approved for intravitreal use to treat neovascular AMD, while bevacizumab is approved for intravenous use as a cancer therapy. However, due to the biological similarity of the two drugs, bevacizumab is widely used off-label to treat neovascular AMD.
U2 - 10.1002/14651858.CD011230.pub2
DO - 10.1002/14651858.CD011230.pub2
M3 - Article
C2 - 25220133
VL - 9
JO - Cochrane Database of Systematic Reviews
JF - Cochrane Database of Systematic Reviews
SN - 1361-6137
M1 - CD011230
ER -