Celltrion has achieved a global first after receiving a marketing authorization for a 100mg/ml biosimilar version of Humira (adalimumab). The European Commission’s pan-European approval follows a positive opinion for the CT-P17 candidate granted by the European Medicines Agency’s Committee for Medicinal Products for Human Use late last year. (Also see "Celltrion Wins Race For High-Concentration Adalimumab" - Generics Bulletin, 11 December, 2020.)
Yuflyma – which will be available as 40mg solution for injection in a pre-filled syringe and pre-filled pen – has...






