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. Author manuscript; available in PMC: 2022 Apr 1.
Published in final edited form as: J Pharm Sci. 2021 Feb 5;110(4):1572–1582. doi: 10.1016/j.xphs.2021.02.003

Table 3.

Percentage of charge variants/ glycans for each biosimilar relative to Humira® given as a range (average). Each biosimilar is compared to a reference Humira® (left of biosimilar column) that was tested simultaneously during analysis.

Charge variants/glycans Humira® Amgevita Humira® Imraldi Humira® Hyrimoz
% basic 19.7–29.3 (24.5) 10.8–16.5 (13.7) 17.5–30.2 (23.9) 8.6–10.9 (9.8) >20.3 12.9–17.7 (15.3)
% acidic 13.1–18.2 (15.7) 17.6–21.7 (19.7) 11.9–18.7 (15.3) 22.6–25.6 (24.1) 9.2–13.9 (11.6) 6.8–10.7 (8.8)
% afucosylated 7.5–13.3 (10.4) 6.7–10.8 (8.8) 1.6–2.3 (2.0) 2.0–3.6 (2.8) 0.5–0.9 (0.7) 2.4–3.2 (2.8)
% sialylated 0.1–0.3 (0.2) 0.5–1.2 (0.9) 0.0–0.6 (0.3) 2.1–3.5 (2.8) <LOQ 0.3–0.5 (0.4)
% galactosylated 16.5–23.0 (19.8) 19.9–39.2 (29.6) 18.3–21.4 (19.9) 19.3–28.3 (23.8) 14.7–23.1 (37.8) 23.7–37.4 (30.6)
% high mannose 5.6–10.6 (8.1) 5.0–8.5 (6.8) 4.4–9.3 (6.9) 5.3–9.9 (7.6) 3.9–6.6 (5.3) 0.9–1.3 (1.1)
% C terminal lysine n/a n/a 5.7–9.6 (7.7) 1.3–3.1 (2.2) 13.3–18.7 (16.0) 3.1–6.0 (4.6)