Table 5.

Relevant pharmacokinetic parameters of depsipeptide


Parameter

Current study

Sandor et al39 
Dose, mg/m2  13   17.8  
AUC, μM · h   6.02 ± 2.93   4.20 ± 2.48* 
Cmax, μM   1.39 ± 0.69   1.02 ± 0.56* 
Cl, L/h/m2  4.81 ± 2.02   10.5 ± 6.4  
Vss, L/m2  3.29 ± 0.94   37.1 ± 47.8  
Uex, % dose   1.18 ± 0.72   Not given  
T1/2, α, h (range)   0.25 (0.1-0.6)   0.42 ± 0.25  
T1/2, β, h (range)   3.67 (2.3-6.5)   8.1 ± 6.0  
MRT
 
0.82 ± 0.37
 
NR
 

Parameter

Current study

Sandor et al39 
Dose, mg/m2  13   17.8  
AUC, μM · h   6.02 ± 2.93   4.20 ± 2.48* 
Cmax, μM   1.39 ± 0.69   1.02 ± 0.56* 
Cl, L/h/m2  4.81 ± 2.02   10.5 ± 6.4  
Vss, L/m2  3.29 ± 0.94   37.1 ± 47.8  
Uex, % dose   1.18 ± 0.72   Not given  
T1/2, α, h (range)   0.25 (0.1-0.6)   0.42 ± 0.25  
T1/2, β, h (range)   3.67 (2.3-6.5)   8.1 ± 6.0  
MRT
 
0.82 ± 0.37
 
NR
 

Data are shown as mean ± SD. For the current study, n = 20; for Sandor et al39 , n = 13. AUC indicates area under the curve; Cmax, maximum clearance; Vss, volume at steady state; Uex, excreted in urine; T1/2, half-life; MRT, mean retention time; NR indicates not reported.

*

Recalculated from Sandor et al.39 

Estimated from a noncompartment method.

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