Biosimilars in Ophthalmology: Financial Implications and Beyond

Ashish Sharma, Nilesh Kumar, N. Parachuri, A. Loewenstein, F. Bandello, B. Kuppermann
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Abstract

Anti-vascular endothelial growth factors (anti-VEGF) have transformed retinal disease management. However, the benefit of anti-VEGF therapy is still limited by the high cost of treatment, specifically in areas where patients are not well covered with insurance and need to pay out of their pocket. Off-label bevacizumab usage has been associated with the risk of infection due to a lack of compounding pharmacies in such areas. In India, the entry of ranibizumab biosimilars has made a significant change and improved access to anti-VEGF therapy for many patients. Recent ranibizumab biosimilar approvals by the European Medicines Agency and the US Food and Drug Administration have brought this therapy to the forefront and have the potential to save the nation’s healthcare spending on these drugs. However, it is yet to be seen how biosimilar anti-VEGF therapy will fit into the crowded space of anti-VEGF therapy globally.
生物仿制药在眼科:财务影响和超越
抗血管内皮生长因子(anti-VEGF)已经改变了视网膜疾病的治疗。然而,抗vegf治疗的好处仍然受到高昂治疗费用的限制,特别是在患者没有很好地覆盖保险并且需要自掏腰包的地区。由于这些地区缺乏复方药房,说明书外贝伐单抗的使用与感染风险有关。在印度,雷尼珠单抗生物仿制药的进入为许多患者带来了重大变化,并改善了抗vegf治疗的可及性。最近,欧洲药品管理局和美国食品和药物管理局批准了雷尼单抗生物类似药,将这种疗法带到了最前沿,并有可能节省国家在这些药物上的医疗保健支出。然而,生物类似药抗vegf治疗如何适应全球抗vegf治疗的拥挤空间还有待观察。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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