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. 2025 Sep 3;42(11):5529–5546. doi: 10.1007/s12325-025-03335-z

Table 3.

Statistical analysis of mirikizumab pharmacokinetic parameters after subcutaneous injection of mirikizumab 300 mg administered by prefilled syringe or autoinjector (Study AMBX)

Parameter Device Geometric mean (geometric %CV)a Geometric LSM Ratio of geometric LSM (AI:PFS) (90% CI)
Cmax (μg/mL) PFS 20.0 (44) 20.3 1.17 (1.07–1.27)
Autoinjector 23.5 (40) 23.7
AUC0–∞ (μg·day/mL) PFS 359 (44) 363 1.15 (1.06–1.24)
Autoinjector 412 (39) 415
AUC0–tlast (μg·day/mL) PFS 355 (44) 359 1.16 (1.07–1.25)
Autoinjector 411 (38) 415
tmax (day), median (min, max) PFS 4.02 (1.88–9.86)
Autoinjector 4.02 (1.91–10.33)
t1/2 (day), geometric mean (min, max) PFS 11.0 (5.75–19.0)
Autoinjector 11.3 (6.20–17.5)
CL/F (L/day) PFS 0.836 (44)
Autoinjector 0.728 (39)
Vz/F (L) PFS 13.3 (38)
Autoinjector 11.9 (31)

AI autoinjector, AUC0–∞ area under the concentration versus time curve from time zero to infinity, AUC0–tlast area under the concentration versus time from time zero to time t, where t is the last time point with a measurable concentration, CI confidence interval, CL/F apparent total body clearance of drug calculated after extravascular administration, Cmax maximum observed drug concentration, CV coefficient of variation, LSM least squares mean, max maximum, min minimum, PFS prefilled syringe, t1/2 half-life associated with the terminal rate constant in noncompartmental analysis, tmax time of maximum observed drug concentration, Vz/F apparent volume of distribution during the terminal phase after extravascular administration

aExcept where noted