Table 2.
Analysis of variance of primary pharmacokinetic variables of fasudil
| Parameter | n | LS mean | LS mean ratio (oral/IV treatment) | ||
|---|---|---|---|---|---|
| treatment A (oral) | treatment B (IV) | Point estimate (%, 90% CI) | Intra-subject CV (%) |
||
| AUC0–tz (μg × h/L) | 14 | 0.29 | 55.58 | 0.52 (0.31–0.87) | 70.46 |
| Cmax (μg/L) | 14 | 1.41 | 100.65 | 1.41 (0.92–2.17) | 56.92 |
AUC0–tz area under the concentration time curve from zero up to the last measured concentration, Cmax highest measured concentration determined in the measuring interval, CI confidence interval, CV coefficient of variation, LS, least square, n number of evaluable subjects included in the model. Results are based on a linear mixed-effects model with sequence, period, and treatment as fixed effects and subject nested within sequence as a random effect