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Table 2 Summary of preclinical PK parameters of imatinib (mean) after a single intravenous or oral dose in preclinical species. Data, mean values

From: Preclinical pharmacokinetic evaluation to facilitate repurposing of tyrosine kinase inhibitors nilotinib and imatinib as antiviral agents

PK parameter

C57BL/6 mice

Prairie dogs

IV Dose (mg/kg)

10

10

No. of animals

3a

5

T1/2 (h)

0.88

2.8 ± 1

MRT (h)

0.77

2.02 ± 0.24

CL (ml/hr./kg)

2212

821 ± 179

Vss (ml/kg)

1697

1666 ± 464

AUC0-inf (ng.hr./ml)

4522

12,558 ± 2189

Oral Dose (mg/kg)

10

30

No. of animals

3a

4

Tmax (h)

1

3 ± 1.15

Cmax (ng/ml)

1468

1677 ± 834

Apparent T1/2 (h)

0.84

2.2 ± 0.6

AUC0-inf (ng.hr./ml)

4852

8092 ± 3012

Bioavailability (%)

107

22

  1. aper time point