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. 2012 Nov 7;62(9):1340–1346. doi: 10.1136/gutjnl-2012-302553

Table 3.

Dosage and time schedule of pegIFN-α2a* treatment for HCV genotype 1b infected chimeric mice

Dose
Donor hepatocytes† No of chimeric mice Inoculum Test compound Level (μg/kg) Concentrtion (μg/ml) Volume (ml/kg) Frequency
A 3 Serum A Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10
B 4 Serum A Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10
C 3 Serum A Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10
D 3 Serum A Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10
A 2 Serum B Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10
C 2 Serum B Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10
A 2 Serum C Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10
C 2 Serum C Peg-IFN-α2a 30 3 10 Day 0, 3, 7, 10

*Pegasys; Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

†The IL28B genetic variation of the donor hepatocytes was indicated in table 2.

HCV, hepatitis C virus; peg-IFN-α, pegylated interferon α.