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. 2018 Oct 3;18:3–14. doi: 10.1016/j.molmet.2018.09.009

Table 2.

Pharmacokinetics of LY3298176.

LY3298176
0.25 mg
N = 6
LY3298176
0.5 mg
N = 12
LY3298176
1.0 mg
N = 5
LY3298176
2.5 mg
N = 6
LY3298176
5.0 mg
N = 5
LY3298176
8.0 mg
N = 7
SAD cohorts SC Route
Cmax, ng/mL 26.0 (29) 57.7 (37) 108 (14) 231 (40) 397 (23) 874 (19)
Tmax, ha 48 (48,48) 48 (24, 96) 24 (8, 48) 24 (24, 96) 24 (24, 72) 48 (24, 72)
AUC0-inf, ng.h/mL 5760 (22) 12000 (24) 22600 (14) 53200 (36) 90500 (15) 169000 (8)
T1/2, hb 116 (94.6, 132) 124 (94.4, 163) 106 (92.9, 117) 120 (102, 137) 123 (99.9, 147) 111 (99.6, 121)
CL/F, L/h 0.0434 (22) 0.0416 (24) 0.0443 (14) 0.0470 (36) 0.0553 (15) 0.0472 (8)
Vz/F, L 7.26 (23) 7.46 (28) 6.76 (18) 8.15 (35) 9.80 (7) 7.55 (4)

Data are Geometric Mean (coefficient of variability CV %), unless otherwise noted. aMedian (minimum, maximum), bGeometric mean (minimum, maximum), Abbreviations: SAD = single ascending dose, Cmax = maximum observed drug concentration, Tmax = time of Cmax, AUC0-inf = area under the concentration time curve from time 0 extrapolate to infinity, CL/F = apparent total body clearance of drug following subcutaneous administration, Vz/F = apparent volume of distribution of drug during terminal phase following subcutaneous administration, N = number of subjects, T1/2 = half-life associated with the terminal rate constant in non-compartmental analysis.