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. Author manuscript; available in PMC: 2007 Sep 25.
Published in final edited form as: J Pharmacokinet Pharmacodyn. 2007 Jan 9;34(2):229–249. doi: 10.1007/s10928-006-9043-z

Table II.

Estimated population pharmacokinetic parameters of saquinavir with the two final models

Model 4 Model 6
Estimate SE (CV %) Estimate SE (CV %)
exp(μCL/F) in L/h 1.26 0.19 (15%) 1.25 0.18 (15%)
βBMI_CL/F* 0.11 0.04 (33%) (p-value = 0.0024)
βDIARRHEA_CL/F* −0.98 0.33 (33%) (p-value = 0.0027)
exp(μV/F) in L 0.86 0.22 (26%) 0,96 0.24 (25%)
exp(μka) in h−1 0.58 0.05 (9%) 0.61 0,05 (8%)
exp(μTlag) in h 1.13 0.12 (11%) 1.12 0.12 (12%)
ω CL/F2 1.41 0.30 (22%) 1.38 0.29 (21%)
ωV/F2 2.43 0.65 (27%) 2.45 0.60 (24%)
ωka2 0.22 0.07 (29%) 0.17 0.05 (28%)
ωTlag2 0.51 0.13 (25%) 0.53 0.12 (23%)
σ2 in (ng/ml)2 85.3 12.5 (15%) 85.7 12.8 (15%)
*

Effect on log(CL/F)