FDA approves Samsung Bioepis’ Epysqli (eculizumab-aagh) as a biosimilar to Soliris (eculizumab)

Samsung Bioepis

22 July 2024 - Epysqli is approved for the treatment of patients with paroxysmal nocturnal haemoglobinuria and atypical haemolytic uremic syndrome.

Samsung Bioepis announced today that the US FDA has approved the biologics license application for Epysqli (eculizumab-aagh) as a biosimilar to Soliris (eculizumab).

Read Samsung Bioepis press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Outcome , Medicine , US , Biosimilar