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. Author manuscript; available in PMC: 2009 Sep 4.
Published in final edited form as: J Biopharm Stat. 2008;18(6):1063–1083. doi: 10.1080/10543400802369004

Table 1. Published KETO and MDZ Data Sets.

Sources dose
(mg)
sample size per subject
(time frame)
Size
(M/F)
meal
KETO
(Gascoigne 1981) 200 capsule 5(1 – 24h) 3(N/A) fasting
200 solution 5(1 – 24h) 3(N/A) fasting
100,200,400 tablet 8(0.5-48h) 12(N/A) meal
200 solution 8(0.5-48h) 12(N/A) meal
(Daneshmend 1981) 200, 400 tablet 14(0.5 – 48h) 28-44 6(6/0) meal
(Daneshmend 1983) 200 tablet, 7(0-24h) 10(0.5-8h) 8(8/0) fasting
(Daneshmend 1984) 200, 400, 600 13(0.5, 32h) 8(3/5) meal
800, tablet (20-31)
(Huang 1986) 200 solution suspension, tablet 12(0.5-48h) 24(24/0) fasting
200, 400, 800 solution. 12(0.5-48h) 12(24/0) fasting
(FDA 1999) 200 tablet 17(1/4-24h) 39(39/0) fasting
200 tablet 17(1/4-24) 23(24/0) meal
(FDA 1999) 200 tablet 15(1/3-48) 24(24/0) fasting
200 tablet 15(1/3-48) 17(17/0) meal

MDZ :
(Lee 2002) 2 IV 27(1/2-6h) 12(6/6) fasting
(Tsunoda 1999) 2 IV 12(1/4-8h) 9(6/3) fasting

In the original paper, MDZ was through IV fusion in a very short period to 2mg, we used the portion of data after fusion and assume IV bolus administration.