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. 2005 Mar 9;5:4. doi: 10.1186/1471-2210-5-4

Table 3.

Population pharmacokinetic parameter estimates for the typical individual after administration of cladribine as; an infusion, orally or subcutaneously. The relative standards errors are given in parentheses. The estimates of intersubject variability are given as coefficients of variation (%).

Parameter Population average Interindividual variability
Estimate (RSE%)1 Estimate % (RSE%)
Clearance (L/h) 39.3 (4.9) 54 (17)
V1 (L) 71.7 (13) 34 (62)
Q2 (L/h) 51.1 (6.8) 61 (17)
V2 (L) 475 (1.8) 70 (31)
Q3 (L/h) 105 (21) 61 (17)
V3 (L) 73.6 (13) 61 (17)
Oral Ka (h-1) 1.31 (14) 75 (50)
Oral F 0.353 (7.9) 4.1 (63)
Subcutaneous Ka (h-1) 2.48 (9,6) N.E.

Parameter Infusion (RSE %) Oral (RSE %) Subcutaneous (RSE %) IIV3 (RSE %)

Residual error2
Proportional 0.191 (8.2) 0.232(9.8) 0.162 (8.8) 24 (28)

1 Rellative standard error. given as %.

2 Residual error presented as population average of estimate and relative standard error in parentheses.

3 Interindividual variability in residual variability expressed as coefficient of variation

Abbreviations: CL, clearance from central compartment; V1, V2 and V3, central and peripheral volumes of distribution, Q2 and Q3, intercompartmental clearances; Ka, absorption rate constant (hour-1); F, bioavailability of drug; N.E., not estimated