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. 2019 Jun 27;38(3):765–775. doi: 10.1007/s10637-019-00815-2

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