Korea Biomedical Review reported that the 24 week results from Celltrion’s Ph III trials of CT-P42 (aflibercept) demonstrate equivalence and similarity to Regeneron’s Eylea®. CT-P42 met secondary endpoints of efficacy, safety, and immunogenicity when compared with Regeneron’s Eyela®. Celltrion intends to file an ABLA for CT-P42 in at least the US and Europe later in 2023.
We have previously reported on the Celltrion IPR challenges to Regeneron’s key aflibercept patents in the US.