Skip to main content
. 2013 Jan 30;8(1):e54522. doi: 10.1371/journal.pone.0054522

Table 1. Pharmacokinetic parameters for belinostat after 30 min i.v. infusion in Phase I trial.

Substance Parameter* 600 mg/m2 900 mg/m2 1200 mg/m2 1400 mg/m2
Belinostat No. of Patients 3 3 6 5
Cmax, µmol/L 88.2±8.5 98.5±29.7 153.5±50.4 174.4±48.3
Tmax, h 0.33±0.14 0.42±0.14 0.64±0.10 0.40±0.14
AUC0–24 h, h× µmol/L 61.3±1.2 70.0±17.3 112.6±37.1 149.0±46.2
T1/2, h 3.54±0.34 4.07±0.39 4.14±0.42 3.54±0.50
CL, L/h 52.6±3.8 70.5±17.9 54.6±15.8 53.0±16.2
Vz, L 268.3±26.6 409.2±76.7 304.9±185.6 279.1±120.8
Belinostat-G AUC0–24 h, h× µmol/L 286.5±36.6 302.1±54.8 514.1±41.4 575.1±154.0
Relative Exposure Bel-G/Bel AUC ratio 4.79±0.46 4.22±0.15 4.82±1.80 4.13±0.68

Abbreviation: Cmax, maximum concentration; Tmax, time to maximum concentration; AUC0–24 h, area under the curve from 0 to 24 h; T1/2, half-life at the elimination phase; CL, clearance; Vz, volume of distribution. *Mean ± SD; AUC ratio was calculated based on AUC0–24 h of Bel-G (belinostat-G) over AUC0–24 h of Bel (belinostat).