Table 2.
Summary of pharmacokinetic parameters of total radioactivity and unchanged rucaparib
| Parameter | Total radioactivity in blood and plasma, mean ± SD | Rucaparib concentration in plasma, mean ± SD | ||
|---|---|---|---|---|
| Plasma | Blood | Blood to plasma ratio | ||
| Cmax, ng Eq/mL or ng/mL | 880 ± 309 | 882 ± 355 | 1.00 ± 0.12 | 428 ± 154 |
| tmax, ha | 4 (0.933–8.00) | 4 (0.933–8.00) | – | 4 (0.933–8.00) |
| AUC0-t, ng Eq h/mL or ng h/mL | 24,100 ± 8580 | 18,100 ± 5460 | – | 8950 ± 3230 |
| AUC0-inf, ng Eq h/mL or ng h/mL | 30,000 ± 7810 | 25,500 ± 5510 | 0.781 ± 0.041 | 9340 ± 3480 |
| t1/2, h | 30.4 ± 8.89 | 28.3 ± 8.49 | – | 25.9 ± 10.1 |
| CL/F, L/h | 19.6 ± 4.83 | 22.6 ± 2.22 | – | 73.9 ± 45.5 |
| Vd/F, L | 814 ± 129 | 911 ± 246 | – | 2300 ± 490 |
atmax presented as median (range)
AUC0-inf area under the concentration-time curve from time zero to infinity, AUC0-t area under the concentration time curve from time zero to time of last measurable concentration, CL/F apparent clearance, Cmax maximum concentration, SD standard deviation, t1/2 terminal half-life, tmax time to maximum concentration, Vd/F apparent volume of distribution