INCHEON, Korea – February 12, 2026 – Samsung Bioepis Co., Ltd. has signed a settlement and license agreement with Regeneron concerning the commercialization of OPUVIZ™ (aflibercept-yszy), a biosimilar to Eylea1 2 mg (aflibercept), in the United States (US), following an earlier settlement covering Europe and the Rest of the World (RoW).2 This agreement enables Samsung Bioepis to launch OPUVIZ 2 mg in the US from January 2027. The other terms of the agreement remain confidential.
“With these two consecutive agreements, we are delighted to resolve all pending patent-related matters relating to our aflibercept biosimilar across the world. We are well-positioned to successfully launch our aflibercept biosimilar 2 mg in approved markets, by working closely with healthcare systems, payers, and providers worldwide,” said Linda Choi MacDonald, Executive Vice President and Global Head of Commercial, at Samsung Bioepis. “Together with ranibizumab, our ophthalmology portfolio will continue to increase accessibility and affordability of biologic medicines for patients living with retinal diseases across the world.”
Samsung Bioepis’ OPUVIZ 2 mg (aflibercept-yszy) was approved by the U.S. Food and Drug Administration (FDA) in May 2024.