Iryna Drozd
The US FDA has authorized Regeneron Prescribed drugs’ (NASDAQ:REGN) high-dose (“HD”) model of its blockbuster remedy Eylea (aflibercept).
The brand new formulation permits sufferers to obtain therapy much less often. HD Eylea is dosed each 4 weeks for the primary 3 months, then each 8 to 16 weeks in moist age-related macular degeneration and diabetic macular edema and each 8 to 12 weeks for diabetic retinopathy.
Whereas the usual Eylea dose is 2 mg, HD Eylea is 8 mg.
Approval was based mostly on the outcomes of the ULSAR and PHOTON research which in contrast HD to straightforward Eylea. HD Eylea met the first endpoint, demonstrating non-inferiority and clinically equal imaginative and prescient positive factors to straightforward Eylea at 48 weeks.
Bayer (OTCPK:BAYZF) (OTCPK:BAYRY) has advertising and marketing rights for HD Eylea exterior the US. The drug is beneath evaluation in Japan and by the European Medicines Company.
The FDA issued a Full Response Letter for HD Eylea in June on account of points at a third-party contract producer.
HD Eylea is seen as competing with Roche’s (OTCQX:RHHBY) Vabysmo (faricimab), with the dosing of the latter as sometimes as each 4 months.
Vabyso introduced in CHF 957M (~$1.1B) within the first half of 2023. Eylea had income of ~$2.9B over the identical interval, although that was a 4% decline from the year-ago interval.
