Celltrion Presents One Year Results of Yuflyma (biosimilar, adalimumab) in P-III CT-P17 3.1 Trial for Rheumatoid Arthritis at EULAR 2021

Shots:

• The P-III CT-P17 3.1 trial involves assessing Yuflyma (adalimumab, 40mg, high-concentration formulation, low-volume and citrate-free, q2w, up to 24 wks.) vs reference adalimumab in a ratio (1:1) in 648 patients with active RA
• The one year data demonstrated comparable efficacy of Yuflyma to reference adalimumab in terms of ACR20/50/70 response rates in patients receiving maintenance therapy and who switched from reference adalimumab to CT-P17 @26wks. up to 52wks., ADA and NAb results were also similar in three treatment groups
• Additionally, EC has granted marketing authorization for Remsima SC (infliximab) to be used without IV infusion for RA patients

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