subtracted dose: one with
EVID=2 to get A-value, and another with EVID=1 to get dose to compartment 4
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
On 9/1/2010
I do not think the code below is correct either for Robert's case or for
enterohepatic recycling
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
On 9/1/2010
to the A(1) at time=6.9 (previous event record)
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
On 9/1/2010 5:02 PM, Mark Sale - Next Level Solutions wrote
=THETA^2
In theta-form, the problem has two identical solution
THETA()=SQRT(OMEGA)andTHETA()= -SQRT(OMEGA)
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
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is
exactly the problem in your particular case?
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
On 8/28/2010 8:55 PM, Corrigan, Brian (Clin Pharm) wrote:
Folks
Ayyappa
Most likely, this is a coding error, so it would help if you post the
code of your model.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
On 8/16
Ayyappa
Most likely, this is a coding error, so it would help if you post the
code of your model.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
On 8/16
could be shifted).
I would try both versions to see the differences, and then use the one
that is more convenient to use in the particular situation.
Best regards,
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail
that may influence parent-to-metabolite transformation, you may want to
spend time investigating the entire system rather than only active
metabolite.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky
mentioned:
the mean estimate of OMEGA(1) was 0.0827
does it mean that Nonmem-estimated OMEGA was close to 0.0827 or you
refer to the variances of estimated ETAs?
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail
) as
ETAunif=TRANS(ETAnorm).
Therefore, the true model can be presented (again, exactly) as
CL=POPCL*exp(TRANS(ETAnorm))
This model should be used for estimation and according to Mats, should
provide you the lowest OF
Leonid
--
Leonid Gibiansky, Ph.D.
President
I've seen on a number of examples (of non-linear differential equations
models) the IMP method diverge (by increasing the OF indefinitely,
until it hits infinity). In those cases, IMPMAP was more successful.
Leonid
--
Leonid Gibiansky, Ph.D.
President
to follow what
is going on.
Thanks
Leonid
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Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
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Freeman, Burgess wrote:
Dear NMUsers,
I recently modeled some single dose
.
$SIGMA
1 FIX ; ~ERR
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chenyuh...@netzero.net wrote:
Dear All,
I am working with a Biologic and would like to have a PK
conventional error model of personal
choice (hopefully supported by the data and confirmed by the VPC).
Best !
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Varsha Mehta wrote:
Dear Group:
I hope someone can help me with the following scaling problem.
I have data on two groups that I would like
effect on error (thus
accounting for possible differences in study populations;
Y=IPRED+SE*EXP(ETA(1))*EPS(1)), etc.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
system in terms of differential equations and add AUC
compartment
$DES
...
DADT(5)=A(2)/S2
Values of A(5) at any time is the AUC from time zero up to the current time
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web
MATRIX=S
Could you provide more details of the output ?
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
markus joerger wrote:
dear NONMEM community
Hi Markus,
On a separate note, this does not look like a traditional definition of
IWRES (=IRES/sqrt(variance)):
W=LOG(F)
IRES=DV-IPRE
IWRES=IRES/W
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail
, respectively, and nonmem will interpret it correctly
My guess is that you should set K0=0, and then everything will work as
you intended (the PK model should be identical to the PK part of the PD
model).
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President
discussed various approached to
the problem that you are trying to solve.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
non...@optonline.net wrote:
Leonid
= prediction of VAS
...
Z=DLOG((VPRED/10+THETA(10))/(1-VPRED/10+THETA(10)))
Y= Z + ERR(1)
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non...@optonline.net wrote
-Original Message-
From: owner-nmus...@globomaxnm.com [mailto:owner-nmus...@globomaxnm.com]
On Behalf Of Leonid Gibiansky
Sent: Friday, 11 December, 2009 6:55
To: prhut...@pharmacy.wisc.edu
Cc: NMUSERS@GLOBOMAXNM.COM
Subject: Re: [NMusers] Duration of Absorption Time From Depot (Gut
/default.asp?abstract=1463
Thanks
Leonid
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non...@optonline.net wrote:
Hello,
NONMEM has the following property related
expression for IVIVC (for example, time scaling) to
insert the dose into the depot compartment (as input rate)
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301
of new subjects given population parameters and variance-covariance
matrix. Is this possible? If yes, could you send me a sample code?
Thanks!
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky
(as in your code) but then estimate individual parameters for a
specific subject, based on his data, rather than use random parameters
consistent with the population model.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web
equations) and stiff. Based on the the indirect-response model
simulations considered in your paper, LOQ/2 substitution seems to
provide reasonable results if Laplacian (and thus M2-M3-M4) cannot be used.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President
your data? If you are not satisfied, could you describe the
deficiencies if there are any; these can help to resolve them.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel
Pavel,
Do you have enough RAM? I had something similar once when I used large
size nonmem 7 installation (I do not remember the exact message, but
this part: The system cannot execute the specified program was there
for sure).
Leonid
--
Leonid Gibiansky
)
Initial conditions should be something like
(0,50,100);EMAX
(0, 2, 100) ;E0
Let me know of you have problem with this code, it should work.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky
distributions should always be similar to the observed
distributions even if the model is correct.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Wang
controlled trials) or with the drop-out
models.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Dider Heine wrote:
Dear NMusers:
The Visual predictive check
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e-mail: LGibiansky at quantpharm.com
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Wang, Diane wrote:
Leonid,
Thank you for the explanation. I was writing the response but found
your email stated it even better than what I
is an
appropriate term. You probably mean uncertain ? or unreliable (read:
with large standard errors?).
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Mark
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michael.j.foss...@gsk.com wrote:
Leonid, this is not necessarily true. You may have data that can't be
used to directly add to the model
it :)
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Nick Holford wrote:
Mats,
[This thread contains several quite different directions so I've decided
for all of us, this is still art, not
science; therefore, the time when everything will be done by the
computers is not too close.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel
and
variability of not only primary parameters (such as theta, omega, etc),
but also relations between derived parameters.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767
variables):
W1=SQRT(THETA(...)/IPRED**2+THETA(...))
Y = LOG(IPRED) + W1*EPS(1)
$SIGMA
1 FIXED
Why concentrations were on LOQ? Was it because BQLs were inserted as
LOQ? Then this is not a good idea.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President
estimates),
and it is not important if they are far apart.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Jurgen Bulitta wrote:
Dear Nick,
Dear Paolo
(relative to the y-axis) peaks,
then flip flop is interfering with the model.
Thanks
Leonid
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Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Paolo Denti wrote
variability, and this can be
seen on VPC plots.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Grevel, Joachim wrote:
Dear Hauke,
thanks
.1) Y=PR1
IF (DV.EQ.2) Y=PR2
IF (DV.EQ.3) Y=PR3
B2 and B3 should be positive
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tel:(301) 767 5566
wangx...@umn.edu wrote:
Hi Samer
the model is sensitive to initial values. Try to guess B1, B2, B3 (or at
least B1) based on the observed data. Try B1=-1, B2=1, B3=1,
Also, try to add random effect to B1.
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail
with the simplest model (assuming other diagnostics do not tell you
otherwise).
Thanks
Leonid
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Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Hauke Rühs wrote
I guess, you can safely remove ETA4 on VSS from the model
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Hauke Rühs wrote:
Dear NMusers,
thank you
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web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Brogren, Jacob wrote:
Hi Leonid,
I tried to change to ADVAN8/ADVAN9 and TOL=8. I get the same error message.
By the way, Martin Brgstrand tiped me about (F
You can try
IF(RICH data) THEN
KA=THETA(1)*EXP(ETA(1))
ELSE
KA=THETA(1)
ENDIF
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e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Ethan Wu wrote:
Dear Juergen
I would try
IF(W.LE.0.01) W = 1
Leonid
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Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
hoxu8...@mail.usyd.edu.au wrote:
Dear Nonmem users,
I have been
probability of observing the value as extreme as the final-model
parameter estimates based on the bootstrap distribution (using a percent
of bootstrap estimates that are below or above the final-model. estimate).
Thanks
Leonid
--
Leonid Gibiansky, Ph.D
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Mats Karlsson wrote:
Hi Leonid,
Pls see below.
Mats Karlsson, PhD
Professor of Pharmacometrics
Dept of Pharmaceutical
arm)? Is it always stable (or at least as stable as
BLOCK(2))?
Thanks
Leonid
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Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
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Mats Karlsson wrote:
Hi Steve
model diagnostics)
Thanks
Leonid
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web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
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Mats Karlsson wrote:
Dear Satyendra,
Interesting question. I don’t think
--
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SIMON Nicolas wrote:
Hi All,
We have a dataset with as many dosing (amount and length of infusion) as
patients. Once the final model was defined, I
, this use of the inverse variance-covariance matrix is
somewhat limited.
--
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Bachman, William wrote:
As a clarification
.
As to the 0 to 1 restriction, l(t) is the density, not probability. It
should integrate to one but can be smaller or greater than 1 (any
positive number).
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky
the
files needed to run nonmem (in R, use setwd(NonmemDirName) to do it)
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Ethan Wu wrote:
Dear users,
I am trying
.
Thanks
Leonid
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Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Dong-Seok Yim wrote:
Leonid,
Thank you for your comprehensive comment.
Once I raised this, I wish to ask
are missing VS=V2,
VA=V3 somewhere.
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Dong-Seok Yim wrote:
Hi, colleagues,
I am currently trying to model
function?
The suggestion was to define the renal disease as categorical variable,
and then correct CL, for example:
TCL ~ THETA(1) (for healthy)
TCL ~ THETA(2) (for patients with severe renal impairment)
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President
: if categorical description does not show
any renal impairment effect, it makes no sense to use more complicated
models, and it makes sense to explain dependence of CL on CRCL by WT,
AGE or other available covariates.
Best
Leonid
--
Leonid Gibiansky, Ph.D
Jakob,
The model that I mentioned is not additive; it is multiplicative:
Parameter= MeanValue*Effect1(WT)*Effect2(RF)
but the effect of RF is expressed as a linear function of RF
Effect2(RF) = 1 + THETA()*RF
Leonid
--
Leonid Gibiansky, Ph.D.
President
DADT(1) = -K*A(1) ; plasma C1=A(1)/V1
DADT(2) = K2*A(1)-K23*A(2) ;transit(can be duplicated to increase delay)
DADT(3) = K23*A(3)-K30*A(3) ; intracellular C3=A(3)/V3
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Xiao, Alan wrote:
Dear All,
I know this is an old topic, too, but would like to see the statistics.
When you have a dataset
-pasted after the summary
of replies.
Part 3: CSV file with the original data is copy-pasted after the comments
Part 4: R code that I used to summarize the results is provided
Thanks to all who participated.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm
/publication FINAL model that did
not converge (YES/NO):
8. Define yourself as novice/intermediate/experienced Nonmem user:
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301
(within the dose/concentration range of your data)
Leonid Gibiansky, Ekaterina Gibiansky,Tarundeep Kakkar, Peiming Ma,
Approximations of the Target-Mediated Drug Disposition Model and
Identifiability of Model Parameters, PAGE 17 (2008) Abstract 1269
[www.page-meeting.org/?abstract=1269]
http
capabilities. I think the OS manages to put active problems to RAM and
non-active ones to swap space so that overall performance is not
affected, but I am not sure, hence the question.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web
time. Is it better (in terms of the run time) to use standard
sizes, or big is OK if you have enough RAM?
Thanks!
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
be omitted. Or you can use separate errors
for each CMT:
Y1=F+F*EPS(1)
Y2=F+F*EPS(2)
Y=R1*Y1+R2*Y2
--
S2= V2 should help to get SE. If not, try MATRIX=S on $COV line.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e
Huali
Even if it gives a good fit, S2=V1 is still an error. You may try to
assume that V2=V1, and then S2=V2=V1, it is fine, but in the current
form, equations are incorrect
Thanks
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web
; then, the difference gradually declined.
Apart from the times when the rate of concentration changes was very
high (concentration changed significantly within 1-2 minutes) the
difference between arterial and venous concentrations was negligible.
Leonid
--
Leonid Gibiansky
dependence of CL on WT (if any is noticeable) for very young kids could
be attributed to maturation and explained by AGE covariate
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel
, it
is not a substitute for the real data. Even with optimal design of the
pediatric study (with the same 20 subjects, 3 optimal sample points) I
bet you would gain by using adult data as well.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web
is optimal. I think one should use both datasets together (in the
specific case that was described) and it looks like we are in agreement
on this point.
Regards,
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
andreas lindauer wrote:
Dear NMusers,
I have a question regarding simulations for a VPC. When a combined
residual error is used it happens
/about/major/nhanes/nh3data.htm
Data can be sampled from this collection, or if needed, described in a
parametric way to sample from a derived distribution.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail
output (error messages if any)
Leonid
--
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President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Jian Xu wrote:
Dear all,
I did a Pop PK a year ago in NM V, and got a stable model
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Ribbing, Jakob wrote:
Hi all,
I think that Paul stumbled on a rather important issue. The SE of the residual
*THETA(3)+THETA(4))
Y=F*(1+SQRT(THETA(3))*ERR(1))+SQRT(THETA(4))*ERR(2).
also, if you take the square of SE% in thetas, you will see that it
nearly matches SE% for SIGMAs, as it should
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web
per embryon, it is unlikely that you can
distinguish between intra and inter subject variability, so I would put
everything to noise (sigma).
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky
)
$TABLE ID TIME CMAX TMAX CC2 CC7 CC8
The last record of each patient should provide desired values.
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Paul
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
-
$PRED
CE=PROP ; define exposure: concentration, AUC or anything else
;PD
EMAX=THETA(1)*EXP
statements.
Best regards,
Jeroen
J. Elassaiss-Schaap
Scientist PK/PD
Organon NV
PO Box 20, 5340 BH Oss, Netherlands
Phone: + 31 412 66 9320
Fax: + 31 412 66 2506
e-mail: [EMAIL PROTECTED]
-Original Message-
From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED]
On Behalf Of Leonid Gibiansky
to be computed and replaced by a particular number, X is the
number of elements required for implementation of PRIOR)
etc
$TABLE ...COM(x+1)=G11 ..
I have not used this combination, so this is the untested idea.
Leonid
--
Leonid Gibiansky, Ph.D.
President
det(aa)
[1] -2945
Leonid
--
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:(301) 767 5566
Sam Liao wrote:
Dear NONMEM users:
Can someone please help me to solve this problem
be time varying. In the example proposed in the NONMEM help the covariate
proposed for use in $MIX is AGE. If AGE is properly recorded in the data set
then AGE is guaranteed to be a time varying covariate!
Nick
Leonid Gibiansky wrote:
Nick,
I am not sure that the entire idea is correct: subject can
in
the example above).
Nick
Leonid Gibiansky wrote:
Nick,
I think you are reading it incorrectly. I would guess that for a long-term
study you may relate
probability of response to either baseline age or to the end-of-study age, or
to any other age in
between, but this value should be one per
Use S2=V/1000 instead of S1=V/1000
Leonid
Tausif Ahmed wrote:
Dear All,
I am new to the field of POP-PK.
We are developing a POP-PK model for our in-house drug. The conc. are in
ng/mL and dose is in mg.
The drug is administered *orally* and follows *1-compartment* model. It
has a short
In Nonmem V (and VI as well), you can put a unit dose to compartment 1, and then estimate
bioavailability F1
F1=THETA(...)*EXP(ETA(...))
In Nonmem VI, you can directly supply initial conditions to the compartmental amounts via parameter
A_0(1), e.g.,
A_0(1)=THETA(...)*EXP(ETA(...))
(see
TIME is not reset, it is counted from the first dose in this example. To describe the model you need
to introduce TAD (time after the most recent dose) into the data set and use it for FLAG reset:
IF(TAD.GT.LAG) FLAG=1
Same with occasion, it would be best to introduce variable OCC (occasion, 1
Should not be a problem for oral administration. If IV, make sure that trough observation records
are before the dosing records (time can be the same, but they should be ordered correctly).
Leonid
Ying HONG wrote:
Dear NMusers,
A single-dose of drug was given to healthy volunteers and a PK
Dear All,
Could anyone help me to interpret ETAbar p value? I have:
TOT. NO. OF OBS RECS:1486
TOT. NO. OF INDIVIDUALS: 213
ETABAR: -0.52E-02 -0.27E-01 -0.93E-01
P VAL.: 0.90E+00 0.24E+00 0.81E-04
ETA1 ETA2 ETA3
ETA1 4.08E-01
ETA2 2.26E-01 2.31E-01
ETA3
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