TABLE 5

Pharmacokinetic Parameters of ABT-806i and ABT-806

Cohort (ABT-806 dose group)ABT-806i (mg)ABT-806 (mg/kg)nTmax (hr)Cmax (μg/mL)Cmax/dose (μg/mL)/(mg/kg)T1/2 (d)*AUC (mg*h/mL)AUC/dose (mg*h/mL)/(mg/kg)CL (mL/h)
ABT-806i (week 1, day 1)
 13–5N/A60.41 ± 0.461.61 ± 0.5023.4 ± 5.26.0 ± 1.50.274 ± 0.0804.07 ± 1.1019.4 ± 6.6
 2 (18 mg/kg)3–5N/A60.11 ± 0.041.62 ± 0.3222.2 ± 4.75.6 ± 1.50.243 ± 0.0623.36 ± 1.0321.3 ± 6.1
 2 (24 mg/kg)3–5N/A60.15 ± 0.101.75 ± 0.3922.7 ± 5.45.3 ± 2.40.261 ± 0.1133.49 ± 1.9024.5 ± 15.9
 2 (18 and 24 mg/kg)3–5N/A120.13 ± 0.081.69 ± 0.3522.4 ± 4.85.4 ± 1.90.252 ± 0.0883.42 ± 1.4622.9 ± 11.6
ABT-806 + ABT-806i (week 6, day 1)
 2 (18 mg/kg)3–5N/A62.25 ± 0.49531 ± 13629.5 ± 7.614.5 ± 4.399.8 ± 27.95.54 + 1.5513.3 ± 4.6
 2 (24 mg/kg)3–5N/A62.16 ± 0.61742 ± 12830.9 ± 5.38.6 ± 2.3116.2 ± 38.64.84 ± 1.6114.8 ± 5.1
  • * Harmonic mean and pseudostandard deviation.

  • AUC for week 1, day 1 and AUCTAU for week 6, day 1.

  • Tmax = time to maximum concentration in serum; Cmax = maximum observed plasma concentration; t1/2 = terminal elimination half-life; AUC = area under the curve; CL = clearance; N/A = not applicable.