USA-based AbbVie (NYSE: ABBV) and Regenxbio (Nasdaq: RGNX) recently presented data from a Phase II study of its lead diabetic retinopathy (DR) and neovascular age-related macular degeneration (nAMD) gene therapy candidate, RGX-314, at the American Society of Retinal Specialists (ASRS) annual meeting, which took place on July 13-16.
RGX-314 has the potential to address a key unmet need for drugs that reduce patient burden and compliance-related issues among diabetic macular edema (DME) patients, says data and analytics company GlobalData.
Currently, patients receiving anti-vascular endothelial growth factor (VEGF) therapy for DME are obliged to visit the hospital six to eight times a year on average. However, despite being an anti-VEGF therapy, similar to many other treatments for DME including the gold standard Bayer’s (BAYN: DE) Eylea (aflibercept), RGX-314 is unique among anti-VEGF treatments as it is a gene therapy, and therefore offered as a one-time treatment.
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