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Celltrion Reports the MAA Submission to the MFDS Korea for CT-P47 (biosimilar, tocilizumab) to Treat Various Indications  

Shots:  

  • The submission was based on the results from the P-III clinical trials evaluating the equivalence & similarity of CT-P47 vs Actemra (tocilizumab) in patients (n=471) with rheumatoid arthritis (RA)  
  • Moreover, based on these results the company also expects to accelerate its marketing authorization application across Canada & other countries. The company expects to receive approval by the year 2025 
  • Actemra is an interleukin inhibitor that functions by reducing inflammation through the inhibition of IL-6 protein  

Ref: Celltrion  | Image: Celltrion | Press Release

Related News:- Alvotech and Teva’s Simlandi (Biosimilar, Humira) Receives the US FDA’s Approval for the Treatment of Multiple Indications 

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