Hi,
I have concentration data from 4 clinical trials and one of those might have
a lag time. A nonlinear model was used to fit the data.
So I need to incorporate lag time into the differential equations. Does
anybody know how to do this?
Many thanks in advance.
Best,
Kehua
Dear NONMEM users,
I did case deletion diagnostic on my model and foud that there might be some
individuals deviate the population. Then I want to try extracting the
individual likehoods to find out those individuals.
Could anybody give me some guidence to do this? Many thanks in advance.
Best
Dear NONMEM users,
I am trying to install NONMEM 7 and G95 on a server.
There is problem when testing the compiler, Pdx-pop says:
>Testing GNU g95 Fortran
>>>ld: cannot open output file C:\gmtest.exe: Permission denied
Looks like I do not have the right. Can I avoid the 'C:\' disk? If so,
Dear NMusers,
I am trying the joint modeling of disease progress and dropout model. NONMEM
did not indicate any error, but it looks like did not run it and there is no
results.
I am following Chuanpu Hu and Mak E. Sale's method. Our disease progress
model isy= base + (slope * time). Please fi
Dear NMusers,
We are trying to do VPC based on a joint disease progress and dropout model.
But we did not get any results from the simulation. Does anybody have any
suggestions?
Thanks a lot.
Kehua
The control stream are below,
$SUBS ADVAN6 TOL=6
$MODEL COMP=(CUMHAZ)
COMP=(HZLAST)
$PK
NDIF
> ELSE ; after event so convert to missing
> DVX=0
> DVIX=DVID
> MDVX=1
> ENDIF
>ENDIF
>
>
> $TABLE ID TRT TIME DVX DVIX MDVX
> NOAPPEND ONEHEADER NOPRINT FILE=joint.fit
>
> First subject in data.csv
>#ID TR
Hi,
We have a data file with 250,000 simulated patients, and we want to estimate
a parameter in NONMEM using a different set of 50 patients at a time (5,000
replicates, but not bootstrapping). Is there an easy way that anybody knows
to automatically repeat the parameter estimation while substitut
Hi,
I am trying to include the protein binding in my model and to estimate the
unbound plasma concentration, using the total plasma concentration. The drug
was taken orally.
It seems that I can write the differential equations as below. A(2) and
A(3) represent the unbound and bound amount, respec
Dear NONMEM users,
I am working on a model in asthma patients and trying to build a model of
FEV1, which is the evaluation of lung function.
I have 500,000 genotyping data. First, I screened the genotyping data by
running GWAS to find out the potential genotyping data, which gave me about
60 g
Dear NONMEM users,
I am trying to build a model to describe the drug toxicity on neuropathy.
Since I am having dose and toxicity data, the K-PD model was applied in our
model. The distribution of baseline is heavily left skewed. So I am also
trying included the Box-cox transformation to get a accu
either.)
$DES
DADT(1)=-KDE*A(1)
VIR=A(1)*KDE
IRG=VIR
COEF=1-(IRG*EMAX/(EDK50+IRG))
DADT(2)=KIN-KOUT*COEF*A(2)
$ERROR
IPRED=F
IRES=DV-IPRED
IF (F.EQ.0) FX=1
W=F+FX
IWRES=IRES/W
Y = F + ERR(1)+F*ERR(2)
-- Forwarded message --
From: kehua wu
Date: Mon, Aug 12, 2013
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