On 15 April 2024, Fresenius Kabi announced its US launch of Tyenne® (tocilizumab-aazg), biosimilar to Roche’s Actemra® (tocilizumab) in both intravenous and subcutaneous formulations. These formulations were FDA approved on 5 March 2024. Tyenne is the third biosimilar product Fresenius Kabi has launched in the US.
Fresenius Kabi launched Tyenne® in Europe as the first to market biosimilar in November 2023 in both IV and subcutaneous formulations.