The first biosimilar with non-Hodgkin’s lymphoma (NHL) indications, Celltrion’s Truxima (rituximab-abbs), has passed the US Food and Drug Administration (FDA) approval process, becoming also the first Rituxan (rituximab) biosimilar authorised in the US.
Launch plans for Truxima remain unclear, for now. While the Korean firm and commercialisation partner Teva earlier this year announced...






