Phase III trials show promise for AMD, DR
The neovascular, or "wet," form of AMD is much less prevalent but is responsible for ~90% of the severe vision loss associated with AMD.3 The most promising results to date have come from drugs that inhibit the activity of vascular endothelial growth factor (VEGF), a critical pro-angiogeni...
Saved in:
Published in | Ophthalmology Times Vol. 33; no. 22; p. 14 |
---|---|
Main Authors | , , |
Format | Trade Publication Article |
Language | English |
Published |
Monmouth Junction
MultiMedia Healthcare Inc
15.11.2008
|
Subjects | |
Online Access | Get full text |
ISSN | 0193-032X 2150-7333 |
Cover
Summary: | The neovascular, or "wet," form of AMD is much less prevalent but is responsible for ~90% of the severe vision loss associated with AMD.3 The most promising results to date have come from drugs that inhibit the activity of vascular endothelial growth factor (VEGF), a critical pro-angiogenic signaling molecule.4 As of this writing, two anti-VEGF drugs have been approved by the FDA for this indication: pegaptanib (Macugen, OSI EyeTech) was approved in December 2004, and ranibizumab (Lucentis, Genentech) was approved in June 2006. Ranibizumab, a fragment of an anti-VEGF monoclonal antibody, has been most effective in clinical trials.5 It is the first treatment for wet AMD that has been shown to improve vision in clinical trials (five to 10 letters on the Early Treatment Diabetic Retinopathy Study [ETDRS] chart); existing therapies such as pegaptanib and photodynamic therapy (PDT) with verteporfin (Visudyne, Novartis) merely slow the rate of vision loss. |
---|---|
ISSN: | 0193-032X 2150-7333 |