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. 2020 Feb 3;12(2):121. doi: 10.3390/pharmaceutics12020121

Table 4.

Plasma pharmacokinetic parameters of ABN401 in beagle dogs following intravenous (IV) and oral (PO) administration of 1, 5, and 10 mg/kg body weight (mean ± SD).

Dose (mg/kg) T1/2 (h) Cmax (ng/mL) Tmax (h) AUClast (h.ng/mL) AUCinf (h.ng/mL) MRTlast (h) BA (%)
IV, 1 1.9 ± 0.7 308.1 ± 270.8 0.083 266.3 ± 104.7 286.8 ± 107.7 1.5 ± 0.7 NA
PO, 1 9.4 ± 3.2 8.0 ± 3.8 1.3 ± 0.6 75.4 ± 42.0 96.2 ± 40.7 7.6 ± 2.5 28.3 ± 15.8
PO, 5 7.6 ± 4.5 50.8 ± 12.4 1.5 ± 0.7 408.7 ± 23.0 455.8 ± 28.5 8.6 ± 2.7 30.7 ± 1.7
PO, 5 * 4.9 ± 0.9 60.3 ± 29.1 2.0 ± 0.0 408.8 ± 201.3 425.4 ± 217.8 6.4 ± 0.7 30.7 ± 15.1
PO, 10 7.7 ± 5.8 52.5 ± 13.5 2.0 ± 0.0 302.2 ± 72.0 424.4 ± 186.2 6.3 ± 3.4 11.3 ± 2.7

* without microcrystalline cellulose (MCC), NA: not applicable