
Biocon Ltd. has announced the commercial launch of Yesafili (aflibercept-jbvf), a biosimilar to Regeneron's Eylea 2 mg, in the United States, as per the exchange filings.
The product is an FDA-approved interchangeable biosimilar, allowing pharmacy-level substitution in accordance with state laws.
According to the company, Yesafili was commercially launched in the United States on August 3, 2026. The product is a biosimilar aflibercept and is targeted at the international market.
Biocon said Yesafili is an FDA-approved interchangeable biosimilar to Eylea 2 mg. The vascular endothelial growth factor (VEGF) inhibitor is indicated for the treatment of ophthalmology conditions, including wet age-related macular degeneration (AMD), diabetic macular edema (DME), diabetic retinopathy (DR) and macular edema following retinal vein occlusion (RVO).
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As of August 03, 2026, at 11:10 AM, Biocon share price was trading at ₹426.75 per share, reflecting a surge of 0.25% from the previous trading session.
Biocon has commercially launched Yesafili, its biosimilar aflibercept, in the United States. The FDA-approved interchangeable biosimilar expands the company's ophthalmology portfolio and is indicated for the treatment of multiple retinal eye disorders.
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Published on: Aug 3, 2026, 1:21 PM IST

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