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. 2013 May 22;8(5):e63818. doi: 10.1371/journal.pone.0063818

Table 5. Summary of pharmacokinetic parameters.

BMS-936558Dose (mg/kg) N Cmax (µg/mL)g. mean (% CV) Tmax (hours) median (min-max) AUC0-T (µg·h/mL)g. mean (% CV) AUCINF (µg·h/mL)g. mean (% CV) T½ (days) mean (SD)
0.03a 3 1.41 (17) 3.25 (1.8–6.3) 4.20 (151) NR NR
0.1 5 3.52 (129) 0.63 (0.5–3.0) 113 (99) NR NR
0.3 5 6.86 (21) 1.03 (1.0–3.0) 1597 (35) NR NR
1 5 26.8 (13) 1.27 (1.0–4.0) 7377 (17) 8537 (19) 20.6 (2.81)
3 5 80.4 (14) 1.50 (1.3–3.0) 26,189 (17) 28,799 (19) 23.2 (4.69)
10 20 195 (20) 1.75 (1.0–48.0) 74,378 (17) 81,022 (20) 23.7 (4.41)
a

Two subjects in the 0.03 mg/kg dose cohort had serum drug concentrations below the assay lower limit of quantitation for all time points and were excluded from pharmacokinetic statistical analyses.

NR = Not reported; the AUCINF extrapolated area was >20% of the total area resulting in undue potential for error.