# NOT RUN {
library(PopED)
############# START #################
## Create PopED database
## (warfarin model for optimization)
#####################################
## Warfarin example from software comparison in:
## Nyberg et al., "Methods and software tools for design evaluation
## for population pharmacokinetics-pharmacodynamics studies",
## Br. J. Clin. Pharm., 2014.
## Optimization using an additive + proportional reidual error
## to avoid sample times at very low concentrations (time 0 or very late samples).
## find the parameters that are needed to define from the structural model
ff.PK.1.comp.oral.sd.CL
## -- parameter definition function
## -- names match parameters in function ff
sfg <- function(x,a,bpop,b,bocc){
parameters=c(CL=bpop[1]*exp(b[1]),
V=bpop[2]*exp(b[2]),
KA=bpop[3]*exp(b[3]),
Favail=bpop[4],
DOSE=a[1])
return(parameters)
}
## -- Define initial design and design space
poped.db <- create.poped.database(ff_file="ff.PK.1.comp.oral.sd.CL",
fg_file="sfg",
fError_file="feps.add.prop",
bpop=c(CL=0.15, V=8, KA=1.0, Favail=1),
notfixed_bpop=c(1,1,1,0),
d=c(CL=0.07, V=0.02, KA=0.6),
sigma=c(0.01,0.25),
groupsize=32,
xt=c( 0.5,1,2,6,24,36,72,120),
minxt=0.01,
maxxt=120,
a=70,
mina=0.01,
maxa=100)
############# END ###################
## Create PopED database
## (warfarin model for optimization)
#####################################
# very sparse grid to evaluate (4 points for each design valiable)
output <- a_line_search(poped.db, opt_xt=TRUE, opt_a=TRUE, ls_step_size=4)
# }
# NOT RUN {
# longer run time
output <- a_line_search(poped.db,opt_xt=TRUE)
# output to a text file
output <- a_line_search(poped.db,opt_xt=TRUE,out_file="tmp.txt")
# }
# NOT RUN {
# }
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