I am running a simulation with subproblems = 1000. One of the
replicates generates the following error:
PROBLEM NO.: 1 SUBPROBLEM NO.:160
0PRED EXIT CODE = 1
0INDIVIDUAL NO. 79 ID=0.13034000E+04 (WITHIN-INDIVIDUAL) DATA REC
NO. 2
ssion model.
Pete bonate
Peter Bonate, PhD, FCP
-Original Message-
From: [EMAIL PROTECTED] <[EMAIL PROTECTED]>
To: 'Mark Sale - Next Level Solutions' <[EMAIL PROTECTED]>
CC: nmusers@globomaxnm.com
Sent: Mon Mar 19 19:42:18 2007
Subject: RE: [NMusers] General questi
eral question on modeling
> From: "Bonate, Peter" <[EMAIL PROTECTED]>
> Date: Tue, March 20, 2007 8:20 am
> To:
>
> Sometimes these threads kill me. There is a degree of art to
modeling.
> The art is the intangible things that we do during model developmen
FOR DATA:
(E7.0,E10.0,E3.0,E5.0,E7.0,E2.0,E5.0,2E2.0,E9.0,E7.0,2E6.0,5E9.0)
Does anyone know what this error means and how to correct it?
thanks,
pete bonate
Peter L. Bonate, PhD, FCP
Time Magazine Person of the Year for 2006
Genzyme Corporation
Senior Director, Pharmacokinetics
4545
Before I get started I thought I would ask whether anyone knew of any
issues regarding running or installing NM V or VI under Windows Vista?
Thanks,
pete bonate
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior Director, Pharmacokinetics
4545 Horizon Hill Blvd
San Antonio, TX 78229 USA
dows XP
Diane
________
From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED]
On Behalf Of Bonate, Peter
Sent: Thursday, May 10, 2007 9:47 AM
To: nmusers@globomaxnm.com
Subject: [NMusers] Windows Vista
Before I get started I thought I would ask whether anyone knew
any real
value any longer.
Any opinions on the validity of throwing out the data, just running with
the model that ignores the phenomenon and has high residual variability,
or something else I haven't been able to think of would be appreciated.
Thanks,
pete bonate
Peter L. Bonate, PhD
population mean clearance was less than 30% CV. Does anyone know
how to do this a priori? Does this seem to be something new?
Thanks,
pete bonate
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior Director, Pharmacokinetics
4545 Horizon Hill Blvd
San Antonio, TX 78229 USA
[EMAIL PROTECTED
I'd also like to see how correlated COV3 and COV4 are. This may be a
collinearity issue.
pete bonate
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior Director
Clinical Pharmacology and Pharmacokinetics
4545 Horizon Hill Blvd
San Antonio, TX 78229 USA
[EMAIL PROTECTED]
phone: 21
uld expect that your IC50s would be similar regardless of
whether you model mean data or individual-level data.
Hope this helps
pete bonate
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior Director
Clinical Pharmacology and Pharmacokinetics
4545 Horizon Hill Blvd
San Antonio, TX 78229 USA
[E
values as predictors in the imputation process.
pete bonate
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior Director
Clinical Pharmacology and Pharmacokinetics
4545 Horizon Hill Blvd
San Antonio, TX 78229 USA
[EMAIL PROTECTED]
phone: 210-949-8662
fax: 210-949-8219
crackberry: 210-315-2713
The Clinical Pharmacology and Translational Research (CPTR) Section
within AAPS wishes to announce a new award to be presented at the AAPS
Annual Meeting - Outstanding Manuscript in Modeling and Simulation. The
review committee is currently soliciting nominations for the award.
The scientific impa
there might be collinearity issues with CrCL
and weight in the same model, even though they are both significant. Does
anyone have a good argument for using CrCL in the model instead of serum Cr?
Thanks
Pete bonate
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior Director
Clinical P
Every year the Clinical Pharmacology and Translational Research Section
within AAPS recognizes an Outstanding Manuscript in Modeling and
Simulation that advances clinical pharmacology or translational research
through the use of modeling and simulation. Last year's winner was
Kaori Ito, Matt Hutm
Does anyone have the infamous Quinidine dataset from Verme et al. that they can
share with me. Any format would be acceptable.
Thanks
pete
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior Director
Clinical Pharmacology and Pharmacokinetics
4545 Horizon Hill Blvd
San Antonio, TX 78229 US
Is anyone aware of any papers or abstracts using computer-assisted trial design
that incorporates a pharmacoeconomic component to the simulation? Or any pop
pharmacokinetic-pharmacodynamic papers that include the same?
Thanks
Pete bonate
Peter L. Bonate, PhD, FCP
Genzyme Corporation
Senior
Dear Friends,
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1.1656E+02 1.1433E+02 0.E+00 0.E+00
0.E+00
The baseline is 117.7 but DELTA has values of 116.6. I cannot figure out what
NONMEM is doing.
Can anyone offer any suggestions. Thanks, pete bonate
Peter L. Bonate, PhD
Senior Director
Global Head - Pharmacokinetics, Modeling, and
The problem looks like this part of the code:
((CIRC0/A(5))**GAM
Either CIRCO0 or A(5) is equal to zero.
Try this
((CIRC0/A(5) + .01)**GAM
pete
Peter L. Bonate, PhD
Senior Director
Global Head - Pharmacokinetics, Modeling, and Simulation
Global Clinical Pharmacology & Exploratory Develop
m and ask them to contact me.
Thanks,
Pete Bonate
Peter L. Bonate, PhD
Senior Director
Global Head - Pharmacokinetics, Modeling, and Simulation
Global Clinical Pharmacology & Exploratory Development
Astellas
1 Astellas Way, 2N.184
Northbrook, Il 60062
phone: 224-205-5855
fax: 224-205-5
Not just yet. I’ve seen many people just naively bootstrap their dataset. It
may be that your bootstrap datasets do not adequately represent model
development dataset. For example suppose you had 75% sparse data and 25% rich
data in your model development set. It is imperative that your boot
Astellas is a bright spot in the pharmaceutical industry, not just because of
what we do, but in the way we do it. At a time when many pharmaceutical
companies are down-sizing, Astellas is growing. If you are looking for a
company where you can change a life, make a dream come true, and light th
look forward to feedback to make
it better in the future.
Pete Bonate
Peter L. Bonate, PhD
Senior Director
Global Head - Pharmacokinetics, Modeling, and Simulation
Global Clinical Pharmacology & Exploratory Development
Astellas
1 Astellas Way, 2N.184
Northbrook, Il 60062
phone: 224-205
Ann
There is a great book on this by David Foster. It is sold on Amazon but is
kind of expensive.
http://www.amazon.com/Tracer-Kinetics-Biomedical-Research-Model/dp/0306464276
I think this could be an invaluable resource for you.
pete
Peter L. Bonate, PhD
Executive Director
Global Head - Ph
Ken Kowalski published a paper many years ago which I think he called a
semicompartmental method. It was not developed as a population approach and
only applies to single dose data but works really well under those conditions.
It was published in the Journal of Pharmacokinetics and Biopharmace
The Journal of Pharmacokinetics and Pharmacodynamics is soliciting articles for
a themed issue on Recent Advances in Cardiovascular
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You may have found a local minima with the microconstant parameterization.
There generally isn’t any rhyme or reason for why one chooses macro or micro
constants. People will argue that the macro model with Q and Vp is more
interpretable than k12 and k21. That, and scaling reasons, are why one
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Leonid - when you say different. What do you mean? Fixed effect and random
effects? Different OFV?
We did a poster at AAPS a decade or so ago comparing results across different
platforms using the same data and model. We got different results on the
standard errors (which related to matrix
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The Pharmacometrics group in the Clinical Pharmacology and Exploratory
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I've never really been happy with this. It's an unsatisfactory solution. You
have a nonlinear drug. Let's assume you have an approved drug. It's given at
some fixed dose. The clinician wants to know what is the drug's half-life so
they can washout their patient and start them on some other
: Justin Wilkins ; Bill Denney
; Bonate, Peter ;
Niurys.CS
Cc: nmusers@globomaxnm.com
Subject: Re: [NMusers] Assessment of elimination half life of mAb
still, half-life of the linear part could be helpful in cases when
non-linearity plays no significant role in elimination, so we tend to present
A full-time, paid internship in Pharmacometrics or Quantitative Systems
Pharmacology is available at Astellas in the summer of 2022 for approximately
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topics related to mechanistic modeling or pharmacometrics, dependi
In comment to Shan’s statement:
It's my understanding that this flip-flop phenomenon is fundamentally a
mathematical problem -- that is, if we write down a PK model in its analytical
form, it becomes rather easy to understand that swapping the values between ka
and ke (CL/V) would lead to the s
This is also discussed in my book on page 70.
The first definition is simply the ratio of the largest to
smallest eigenvalue
K = L1/Lp (51)
where L1 and Lp are the largest and smallest eigenvalues of
the correlation matrix (Jackson 1991). The second way is to
define K as
K = sqrt(L1/Lp)(5
This is great. Just like the glory days of NMusers. Any moment now Nick Holford
is jointing to chime in.
I’m not an expert in matrix algebra but is the correlation matrix the right one
to be using? We are concerned about inversion of the hessian. That
instability is what affects our paramete
“Dancing with the Stars” is not owned by Astellas.
-Original Message-
From: Ken Kowalski
Sent: Tuesday, November 29, 2022 8:29 PM
To: Bonate, Peter ; 'Leonid Gibiansky'
Cc: 'Matthew Fidler' ; 'Kyun-Seop Bae'
; nmusers@globomaxnm.com; 'Jeroen Elassaiss-Scha
Simulation (PKMS)
Clinical Pharmacology and Exploratory Development (CPED)
Astellas
1 Astellas Way
Northbrook, IL 60062
peter.bon...@astellas.com
(224) 619-4901
Quote of the week –
“Dancing with the Stars” is not owned by Astellas.
-Original Message-
From: Bonate, Peter
Sent
A full-time, paid internship in pharmacometrics is available at Astellas in the
summer of 2024 for approximately 12 weeks. Successful candidates will work
closely with a senior-level pharmacometrician on topics related to population
pharmacokinetics or pharmacometric methods, depending on the in
this started with
NONMEM IV.
There was a history of NONMEM webpage that Icon maintained, but when I checked
today, it no longer looks like it is functional.
https://nonmem.iconplc.com/nonmem_history/NONMEM_history4.pdf
Pete Bonate
Peter Bonate, PhD
Suzerain, New Technologies
Early Development
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