BioBlast w/e 03 Nov 23
Merck announced that the US FDA has approved Keytruda® (pembrolizumab) for the treatment of patients with locally advanced unresectable or metastatic…
Source: lexology.com
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BioBlast w/e 23 Oct 23
Celltrion announced that the FDA has approved its subcutaneous formulation of Zymfentra® (infliximab -dyyb), biosimilar to Janssen’s Remicade®, as…
Source: lexology.com
BioBlast w/e 22 Sep 23
Prestige Biologics, a contract development and manufacturing organization (CDMO), announced it has signed a non-binding MOU with Aurigene…
Source: lexology.com