Despite holding US Food and Drug Administration approval, Biocon looks set to be barred from launching its Yesafili (aflibercept-jbvf) biosimilar to Regeneron’s near $6bn Eylea low-dose 2mg formulation until June 2027 after the originator was granted a permanent injunction.
Judge Thomas Kleeh, presiding over sprawling biosimilar Eylea litigation in the US District Court for the Northern District of West...






