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
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