Amgen will look to kick off March by launching its Bkemv (eculizumab-aeeb) US Food and Drug Administration-approved biosimilar to AstraZeneca’s Soliris (eculizumab) – the first biosimilar to the paroxysmal nocturnal haemoglobinuria (PNH) and atypical haemolytic uraemic syndrome (aHUS) treatment set to reach the US, via its 2020 settlement with the originator.
The California-based biotech will enjoy a non-exclusive, royalty-free, license under US patents and patent applications related to eculizumab and various aspects of the eculizumab product by AstraZeneca’s Alexion
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