The biosimilar will be available in both subcutaneous and intravenous formulations and has nearly all the same indications as ...
A recent study found that combined tocilizumab and glucocorticoid therapy for at least 6 months did not fully eliminate ...
Avtozma, the third biosimilar to Actemra, has received FDA approval for multiple inflammatory diseases and COVID-19, ...
The FDA's approval is grounded in an evidence totality and comprehensive data package, which includes outcomes from a study.
NYU Langone Health in New York City reportedly cancelled the appointments of two transgender children scheduled to receive ...
The FDA has approved a third biosimilar for tocilizumab, called Avtozma, the second such biosimilar to be available in both intravenous and subcutaneous formulations, according to a press release.
Jersey City, New Jersey Saturday, February 1, 2025, 16:00 Hrs [IST] ...
The biosimilar of IL-6 inhibitor tocilizumab, called Tyenne (formerly MSB11456), has been approved for the same indications as Roche’s brand, including rheumatoid arthritis, systemic juvenile ...
The FDA has approved Avtozma® (tocilizumab-anoh), a biosimilar to Actemra®, in both intravenous and subcutaneous formulations.
The new biosimilar, Celltrion’s Avtozma, was approved in both IV and subcutaneous forms to treat inflammatory conditions such as arthritis.
Findings showed tocilizumab-anoh had comparable efficacy, pharmacokinetics, safety, and immunogenicity with Actemra. The Food and Drug Administration (FDA) has approved Avtozma ® (tocilizumab ...
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