Table 3.
Summary of simulation results of PBPK modeling for effect of lusutrombopag with multiple dose of 3 mg or 6 mg on pharmacokinetics of midazolam
| Lusutrombopag dose | Parameter | Geometric mean (90% PI) | Ratio (with/alone)a | |
|---|---|---|---|---|
| Alone | With | |||
| 3 mg | Cmax (ng/mL) | 15.61 (6.36, 39.29) | 16.57 (6.87, 40.58) | 1.05 (1.02, 1.12) |
| AUC (ng h/mL) | 56.20 (16.46, 139.10) | 59.67 (17.78, 143.50) | 1.05 (1.02, 1.12) | |
| 6 mgb | Cmax (ng/mL) | 15.61 (6.36, 39.29) | 17.32 (7.36, 41.55) | 1.10 (1.04, 1.23) |
| AUC (ng h/mL) | 56.20 (16.46, 139.10) | 62.38 (19.01, 146.77) | 1.10 (1.04, 1.23) | |
PI, prediction interval
aMedian (90% PI)
bThe 6-mg dose was tested to achieve comparable exposure at the clinical dose of 3 mg once daily for 7 days in the target patients