Skip to main content
. Author manuscript; available in PMC: 2013 Nov 1.
Published in final edited form as: J Clin Pharmacol. 2011 Dec 14;52(11):1654–1664. doi: 10.1177/0091270011429567

Table III.

Comparison between optimal LSS and reference design for estimating AUCa0-τ after IV MMF dosing

Sampling time (hr) Root mean sMSEb % (AUC0-τ) Mean relative bias (rbias)% (AUC0-τ) Pearson r Percent of subjects with rbias% > 10%
Q 12 hr MMF dosing
Reference design Pre-dose, 1, 2, 4, 6, 8, 10 17.62 9.19 0.97 1.7%
 5-sample LSS 2, 2.5, 3, 5, 6 17.37 9.03 0.97 1.5%
 4-sample LSS 2, 2.5, 3, 6 18.50 9.78 0.97 1.2%
 3-sample LSS 2, 2.5, 5 20.56 10.8 0.97 3.2%

Q 8 hr MMF dosing
Reference design Pre-dose, 1, 2, 4, 6, 8 18.37 10.0 0.97 1.7%
 5-sample LSS 2, 2.5, 3, 4, 6 17.36 9.29 0.97 1.5%
 4-sample LSS 2, 2.5, 3, 5 18.18 9.59 0.97 1.3%
 3-sample LSS 2, 2.5, 5 20.30 11.0 0.98 2.5%
a

AUC0-τ where τ is dosing frequency, so AUC0-12hr for IV MMF dosed Q12 hrs and AUC0-8hr for IV MMF dosed Q8hrs;

b

sMSE: scaled mean square error.