Angiopoietins as Potential Targets in Management of Retinal Disease

Arshad M Khanani,1,2 Matthew W Russell,3,4 Aamir A Aziz,1,2 Carl J Danzig,5,6 Christina Y Weng,7 David A Eichenbaum,8,9 Rishi P Singh3,4 1Sierra Eye Associates, Reno, NV, USA; 2The University of Nevada, Reno School of Medicine, Reno, NV, USA; 3Center for Ophthalmic Bioinformatics, Cole Eye Institute...

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Main Authors: Khanani AM, Russell MW, Aziz AA, Danzig CJ, Weng CY, Eichenbaum DA, Singh RP
Format: Article
Language:English
Published: Dove Medical Press 2021-09-01
Series:Clinical Ophthalmology
Subjects:
Online Access:https://www.dovepress.com/angiopoietins-as-potential-targets-in-management-of-retinal-disease-peer-reviewed-fulltext-article-OPTH
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author Khanani AM
Russell MW
Aziz AA
Danzig CJ
Weng CY
Eichenbaum DA
Singh RP
author_facet Khanani AM
Russell MW
Aziz AA
Danzig CJ
Weng CY
Eichenbaum DA
Singh RP
author_sort Khanani AM
collection DOAJ
description Arshad M Khanani,1,2 Matthew W Russell,3,4 Aamir A Aziz,1,2 Carl J Danzig,5,6 Christina Y Weng,7 David A Eichenbaum,8,9 Rishi P Singh3,4 1Sierra Eye Associates, Reno, NV, USA; 2The University of Nevada, Reno School of Medicine, Reno, NV, USA; 3Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA; 4Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH, USA; 5Rand Eye Institute, Deerfield, FLA, USA; 6Florida Atlantic University, Charles E. Schmidt College of Medicine, Boca Raton, FL, USA; 7Baylor College of Medicine, Houston, TX, USA; 8Retina Vitreous Associates of Florida, St Petersburg, FLA, USA; 9University of South Florida Morsani College of Medicine, Tampa, FLA, USACorrespondence: Arshad M Khanani 950 Ryland Street, Reno, NV, 89502, USATel +775 329-0286Fax +775-329-0849Email arshad.khanani@gmail.comAbstract: The Ang/Tie2 pathway complements VEGF-mediated activity in retinal vascular diseases such as DME, AMD, and RVO by decreasing vascular integrity, increasing neovascularization, and increasing inflammatory signaling. Faricimab is a bispecific antibody that has been developed as an inhibitor of both VEGF and Ang2 that has shown positive results in phase I, II and III trials. Recent Year 1 data from phase III clinical trials YOSEMITE, RHINE, TENAYA, and LUCERNE have confirmed the efficacy, safety, durability, and superiority of faricimab in patients with DME and nAMD. Faricimab, if approved, may significantly decrease treatment burden in patients with retinal vascular diseases to a greater extent than would current standard of care anti-VEGF injections.Keywords: Ang/Tie, faricimab, YOSEMITE, RHINE, TENAYA, LUCERNE
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spelling doaj.art-2dbb17760b0148fd9c76775d32c643de2022-12-21T22:59:50ZengDove Medical PressClinical Ophthalmology1177-54832021-09-01Volume 153747375568504Angiopoietins as Potential Targets in Management of Retinal DiseaseKhanani AMRussell MWAziz AADanzig CJWeng CYEichenbaum DASingh RPArshad M Khanani,1,2 Matthew W Russell,3,4 Aamir A Aziz,1,2 Carl J Danzig,5,6 Christina Y Weng,7 David A Eichenbaum,8,9 Rishi P Singh3,4 1Sierra Eye Associates, Reno, NV, USA; 2The University of Nevada, Reno School of Medicine, Reno, NV, USA; 3Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA; 4Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH, USA; 5Rand Eye Institute, Deerfield, FLA, USA; 6Florida Atlantic University, Charles E. Schmidt College of Medicine, Boca Raton, FL, USA; 7Baylor College of Medicine, Houston, TX, USA; 8Retina Vitreous Associates of Florida, St Petersburg, FLA, USA; 9University of South Florida Morsani College of Medicine, Tampa, FLA, USACorrespondence: Arshad M Khanani 950 Ryland Street, Reno, NV, 89502, USATel +775 329-0286Fax +775-329-0849Email arshad.khanani@gmail.comAbstract: The Ang/Tie2 pathway complements VEGF-mediated activity in retinal vascular diseases such as DME, AMD, and RVO by decreasing vascular integrity, increasing neovascularization, and increasing inflammatory signaling. Faricimab is a bispecific antibody that has been developed as an inhibitor of both VEGF and Ang2 that has shown positive results in phase I, II and III trials. Recent Year 1 data from phase III clinical trials YOSEMITE, RHINE, TENAYA, and LUCERNE have confirmed the efficacy, safety, durability, and superiority of faricimab in patients with DME and nAMD. Faricimab, if approved, may significantly decrease treatment burden in patients with retinal vascular diseases to a greater extent than would current standard of care anti-VEGF injections.Keywords: Ang/Tie, faricimab, YOSEMITE, RHINE, TENAYA, LUCERNEhttps://www.dovepress.com/angiopoietins-as-potential-targets-in-management-of-retinal-disease-peer-reviewed-fulltext-article-OPTHang/tiefaricimabyosemiterhinetenayalucerne
spellingShingle Khanani AM
Russell MW
Aziz AA
Danzig CJ
Weng CY
Eichenbaum DA
Singh RP
Angiopoietins as Potential Targets in Management of Retinal Disease
Clinical Ophthalmology
ang/tie
faricimab
yosemite
rhine
tenaya
lucerne
title Angiopoietins as Potential Targets in Management of Retinal Disease
title_full Angiopoietins as Potential Targets in Management of Retinal Disease
title_fullStr Angiopoietins as Potential Targets in Management of Retinal Disease
title_full_unstemmed Angiopoietins as Potential Targets in Management of Retinal Disease
title_short Angiopoietins as Potential Targets in Management of Retinal Disease
title_sort angiopoietins as potential targets in management of retinal disease
topic ang/tie
faricimab
yosemite
rhine
tenaya
lucerne
url https://www.dovepress.com/angiopoietins-as-potential-targets-in-management-of-retinal-disease-peer-reviewed-fulltext-article-OPTH
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AT danzigcj angiopoietinsaspotentialtargetsinmanagementofretinaldisease
AT wengcy angiopoietinsaspotentialtargetsinmanagementofretinaldisease
AT eichenbaumda angiopoietinsaspotentialtargetsinmanagementofretinaldisease
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