nce we wish to draw
from it.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 5044
F: +64 3 479 7034
Design software: www.winpopt.com
Mark
> But, I have to admit that I'm uncomfortable with the concept
> of the "art" of modeling.
I agree - I like to think of it as a science of modelling - but I have heard
(at conferences) the "science" of modelling referred to as the "art" of
modelling.
> decisions on art? Shouldn't we be
tinuous and in oncology BSA is considered
continuous.
Certainly my approach to the clinical sciences is very much based on renal
function being continuous - this is after all what we teach our students
(future providers).
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharm
nds on what you are developing the
model for...
I'll leave the other questions for the time being.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 5044
F: +64 3 4
Stephen Duffull
([EMAIL PROTECTED]) or Professor Ian Tucker
([EMAIL PROTECTED]) Reference Number: A07/82 Closing Date: 20
July 2007.
http://pharmacy.otago.ac.nz/pages/vacancies.html
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913
Stephen Duffull
([EMAIL PROTECTED]) or Professor Ian Tucker
([EMAIL PROTECTED]) Reference Number: A07/82 Closing Date:
20
July 2007.
http://pharmacy.otago.ac.nz/pages/vacancies.html
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
s with respect to convergence? I believe that the SAEM
algorithm is proven to converge if run long enough - but of course how long
is long enough is for the experts.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New
rval (e.g. 1 dose interval).
[i.e. To be (perhaps inappropriately) provocative, if large estimated BOV is
bad for your drug then all you need to do is make the occasion duration to
be very long :-)]
Just some thoughts.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
Un
Queensland, Australia
Aris Dokoumetzidis, The University of Manchester, UK
Stephen Duffull, University of Otago, NZ
Steven Gilmour, Queen Mary, University of London, UK
Gordon Graham, Pharmacometrics, Pfizer, UK
Heiko Grossmann, Queen Mary, University of London, UK
Iva Gueorguieva, Global
:
Bruce Charles, University of Queensland, Australia
Stephen Duffull, University of Otago, New Zealand
Bruce Green, University of Queensland, Australia
Nick Holford, University of Auckland, New Zealand
Carl Kirkpatrick, University of Queensland, Australia
Diane Mould
abstracts: 11th January 2008
Note: registration, payment and abstract submission can all be done on-line
at the PAGANZ web-site.
*** Numbers are capped at 50 participants! ***
Presenters include:
==
* Chuanpu Hu
* Andrew Hooker
* Nick Denman
* Stephen Duffull
* Nick Holford
* Pavan
ut question that industry, regulatory and academia all
play equally important roles in improving patient care.
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 50
calculate CLCR (based on LBM).
Otherwise limited impact on already busy clinical pharmacy services.
There are other examples (but I'm marking exams right now) but I'm sure
others can comment here too.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmac
ote Einstein) - "the dosing regimen should be as simple
as possible but not simpler..."
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 5044
F: +64 3 479 7034
Design software: www.winpopt.com
se in academic settings that improve patient care [to
respond to Mark's comments] and b) that simplifying the dosing on the drug
label to make the drug "easier to use" doesn't necessarily result in better
patient outcomes.
Regards
Steve
--
Professor Stephen Duffull
Ch
aces available in the Introduction to NONMEM workshop
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 5044
F: +64 3 479 7034
Design software: www.winpopt.com
at:
http://www.paganz.org/default.asp?id=42&keuze=meeting
Kind regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 5044
F: +64 3 479 7034
Design software: www.winpopt.com
wever, e.g. general medical
etc. It would depend on what population you wanted.
However if you're interested in a multivariate distribution (e.g. the joint
distribution of weight and height) then your choices are more limited.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
Sch
d concentration. And observed concentration
perhaps should be termed "assay predicted concentration" while predicted
concentration should be "PK model predicted concentration", but this is a
bit of a mouthful.
Regards
Steve
--
Professor Stephen Duffull
School of Pharmacy
Unive
rds
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 5044
F: +64 3 479 7034
Design software: www.winpopt.com
> -Original Message-
> From: [EMAIL PROTECTED]
> [mail
g a model that allows me to draw appropriately accurate
conclusions. Optimal design is a way that allows investigators to improve
the informativeness of data. Obviously, no data = no information.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
Leonid
> The original question was whether it is beneficial to add
> adult data to the pediatric (in the specific case under
> study). Your previous e-mail could be interpreted as the
> suggestion that one can estimate model parameters with the
> pediatric data alone if the pediatric study des
conducive to a high quality lifestyle.
Specific enquiries may be directed to Professor Stephen Duffull, Chair in
Clinical Pharmacy, School of Pharmacy, Tel 03 479 5044, Email
[EMAIL PROTECTED]
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913
simultaneous analysis with sequential Bayesian analysis. I can't
recall where it was published - but it's worth a read.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [EMAIL PROTECTED]
P: +64 3 479 504
Atul
> It is always a good idea to estimate the allometric
> coefficient if you have adequate (weight ranges, PK sampling
> etc) data collected.
An interesting point. If you estimate the allometric coefficient then it
will almost always give a better fit to your data as your model has more
d
s statistically
better ...
At what stage you consider a covariate to be "fundamental" meaning it should
never be excluded will depend on the circumstance.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: [
aditional VPCs don't work well (note we did this in WinBUGS).
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz
P: +64 3 479 5044
F: +64 3 479 7034
Design software: www.winpopt.com
dvantages of application of DIAG(3) as an
alternative to BLOCK(2).
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz
P: +64 3 479 5044
F: +64 3 479 7034
Design software: www.winpopt.com
.karls...@farmbio.uu.se]
> Sent: Thursday, 16 April 2009 11:07 p.m.
> To: Stephen Duffull; drmo...@pri-home.net;
> nele.pl...@nycomed.com; nmusers@globomaxnm.com
> Subject: RE: [NMusers] OMEGA BLOCK with mixture model?
>
> Hi Steve,
>
> For a one-compartment model I think these are diffe
e the differences between the two data sets
would be to analyse them sequentially, perhaps with consideration for using the
analysis from the Rich data as an informative prior for the analysis of the
Sparse data and see where this leads you.
Kind regards
Steve
--
Professor Stephen Duffull
Cha
Nick
Your approach is an important first step. However, there remains the
possibility of co-dependence in the marginal distribution of the data once you
have included a common fixed effect in your models.
I'm not sure that this can be specifically implemented in NONMEM for odd-type
data. If
gt; Sent: Wednesday, 22 July 2009 5:31 p.m.
> To: Stephen Duffull
> Cc: Nick Holford; nmusers
> Subject: Re: [NMusers] Modeling of two time-to-event outcomes
>
> For 2 event-time responses, without regression, copula models are the
> common way of handling bivariate event time mod
ent?
Yes. I would expect that the degree of co-dependence would decrease.
> It would be helpful to me and perhaps to others if you could give some
> specific example of what copulas contribute.
I haven't seen a PKPD estimation application (yet).
Steve
--
Professor Stephen Duffull
Chai
t hope to account for
co-dependence structure based on fixed effects only.
Steve
--
>
> Stephen Duffull wrote:
> > Hi Nick
> >
> >
> >> I've been hearing about copulas for a couple of years now but
> haven't
> >> seen anything which r
Nick
> I still don't understand what this has to do with 'interval data'.
Read "continuous data".
Steve
--
Mats
Just a comment on your comments below:
"All models are wrong and I see no reason why the exponential error model would
be different although I think it is better than the proportional error for most
situations. "
"Why would you not be able to get sensible information from models that don
Mats
> I think you're missing an important point. As I wrote to Nick, you will
> never get concentrations reported regardless of their value. At some
> point,
> you will only get the information that concentration is below a limit
> (LOQ,LOD,LO?). This you should take into account in your design.
Mats
I agree with Nick. Negative "observed" concns do occur for assays, even in my
limited time working with HPLC I have seen them, however due to LOD/LOQ they
are never really looked for and certainly never reported...
Steve
> -Original Message-
> From: owner-nmus...@globomaxnm.com [
d and
converse in English is essential.
A limited number of places, at a reduced fee, are available to academic
persons. Further details are available upon request to
irene.s...@pkworkshops.com<mailto:irene.s...@pkworkshops.com>.
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
Schoo
knowledge, and factoring in some growth and applying an
equilibrium model, we can predict the required training rate...
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz
P: +6
pline is the total
number of young faculty in pharmacometrics across the world. They say (at
least Stephen Pinker does) that a language is officially dead when less than
6000 children speak it...
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
Universit
Juergen (Bob, Nick, Leonid)
FYI: In WinBUGS I also don't get problems with:
> MU_1=THETA(1)
> EXPP=MU_1+ETA(1)
> EXPW=EXP(-EXPP)
> BIO=1/(1.0+EXPW)
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 913 Dune
t it will deactivate this
endearing Win7 feature.
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz<mailto:stephen.duff...@otago.ac.nz>
P: +64 3 479 5044
F: +64 3 479 70
related to the various
software (incl. pfim).
Kind regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz
P: +64 3 479 5044
F: +64 3 479 7034
W: http://pharmacy.otago.ac.nz/profiles
n to do
simulation ...
You can easily call NONMEM (for estimation) from S, R and MATLAB. Hence
simulating the complex data sets and then calling NONMEM for the estimation
process (once the data sets have been reduced to an appropriate size) is
relatively simple.
Regards
Steve
--
Professor Steph
to install NM (at least I can't do it).
There was a thread about this recently which gave details on how to disable
this feature of Win7.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 Dunedin
New Zealand
E: stephen.duff
e. to
reduce bias in estimates of the population mean parameter values).
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz<mailto:stephen.duff...@otago.ac.nz>
P: +64 3 479 5044
F: +64
mbio.uu.se]<mailto:[mailto:mats.karls...@farmbio.uu.se]>
Sent: Tuesday, 2 November 2010 3:11 p.m.
To: Stephen Duffull; 'Nick Holford';
nmusers@globomaxnm.com<mailto:nmusers@globomaxnm.com>
Subject: RE: [NMusers] Rational of using IOV
Hi Steve,
I think we can apply some mechanisti
nce routes. Once you have something that you
think describes the biology then I think it would be important and interesting
to explore inclusion of hierarchical random effects.
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 D
this nature (you need to join up at
http://lists.otago.ac.nz/listinfo/popdesign to use it).
I am not aware of any limited sampling software.
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 Dunedin
New Zealand
E: s
Hi Li
I’m not aware of specific interpretations for negative shrinkage other than the
evaluation of the SD of the ETAs is greater than the estimate of the sqrt of
OMEGA for the same parameter. Since OMEGA itself is an estimate then ETA
shrinkage may occur due to either the EBEs being underdisp
rbitrary cut-off. But the devil here lies with
the non-regulatory work where you may not have defined these boundaries a
priori.
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz
P: +64
the results you're stuck. Would not a
pragmatic view be appropriate? Report the outcomes of the BS runs as they
occurred but then select those runs that terminated appropriately? Otherwise
BS is too risky...
Steve
PS All models are wrong :-)
--
>
>
> On 7/10/2011 2:57 P
Hi Charles
The choice of the df of the Wishart should be based on what your prior
information provides not on what the posterior distribution tells you. I
suspect, if your data is relatively uninformative then a sensitivity analysis
will show that the posterior is sensitive to the prior. It w
le
8256 Union Centre Blvd, IP-351
West Chester, OH 45069
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(513) 634-9827
From: owner-nmus...@globomaxnm.com<mailto:owner-nmus...@globomaxnm.com>
[mailto:owner-nmus...@globomaxnm.com] On Behalf Of Stephen Duffull
Sent: Monday, January 30, 20
Hi
An appropriate value for dof of the IW is difficult to determine. While it can
be set at n-1 from a prior this is somewhat arbitrary. It is not in this sense
like a t-distn where we calculate dof in this manner.
You would have to get a feeling for the degree of spread in your deviates give
the system.
Regards
Steve
--
Professor Stephen
Duffull<http://pharmacy.otago.ac.nz/our-people/academic-staff/stephen-duffull>
Chair of Clinical Pharmacy
School of Pharmacy
University of Otago
PO Box 56 Dunedin
New Zealand
E: stephen.duff...@otago.ac.nz<mailto:stephen.duff...@otago.ac.nz&
It turns out that there are many symmetric matrices where off-diagonals are
between -1 and 1 that have negative determinants. Just to add my 2c there are
also non-positive definite symmetric matrices that have positive determinants.
Some are obvious and some are not. So if you were to paramete
l of Pharmacy and Pharmaceutical
Sciences, University of Manchester, UK. His research interests are in
population and physiologically based pharmacokinetics.
Stephen Duffull is Professor of Clinical Pharmacy at the University of Otago,
Dunedin, New Zealand. He runs a modelling and simulation lab within
ysis.
Faculty
Leon Aarons is a Professor in the School of Pharmacy and Pharmaceutical
Sciences, University of Manchester, UK. His research interests are in
population and physiologically based pharmacokinetics.
Stephen Duffull is Professor of Clinical Pharmacy at the University of Otago,
Dunedin, New Zea
ysis.
Faculty
Leon Aarons is a Professor in the School of Pharmacy and Pharmaceutical
Sciences, University of Manchester, UK. His research interests are in
population and physiologically based pharmacokinetics.
Stephen Duffull is Professor of Clinical Pharmacy at the University of Otago,
Dunedin,
l of Pharmacy and Pharmaceutical
Sciences, University of Manchester, UK. His research interests are in
population and physiologically based pharmacokinetics.
Stephen Duffull is Professor of Clinical Pharmacy at the University of Otago,
Dunedin, New Zealand. He runs a modelling and simulation lab wi
Hi Bernard
There is an email listserver set up specifically for optimal design questions.
See: http://lists.otago.ac.nz/listinfo/popdesign
The software developers for PopDes are also members of this list.
Regards
Steve
--
Professor Stephen Duffull
Chair of Clinical Pharmacy
School of
d to seeing you next January!
Regards,
Steve Duffull
On Behalf of the PAGANZ Organising Committee
--
Professor Stephen Duffull,
School of Pharmacy,
University of Otago,
PO Box 56,
Dunedin 9054,
New Zealand.
Email: stephen.duff...@otago.ac.nz
...@otago.ac.nz)
Best regards
Steve
…....………
Stephen Duffull I Professor of Clinical Pharmacy | Dean
Otago Pharmacometrics Group
New Zealand’s National School of Pharmacy | Te Kura Mātauraka Wai-whakaora
University of Otago | Te Whare
Santosh
Perhaps a more pertinent question is – Why do you want to know half-life?
Steve
…....………
Stephen Duffull I Professor of Clinical Pharmacy | Dean
Otago Pharmacometrics Group
New Zealand’s National School of Pharmacy | Te Kura
, since this is generally
not the case (i.e. the assay result is not reported exactly) then I agree it
will not provide useful information to the estimation process.
Cheers
Steve
…....………
Stephen
Duffull<http://www.otago.ac
Stephen Duffull | Professor
Otago Pharmacometrics Group
School of Pharmacy | He Rau Kawakawa
University of Otago | Te Whare Wānanga o Otāgo
Dunedin | Ōtepoti
Aotearoa New Zealand
Ph: 64 3 479 5099
-Original Message-
From: owner-nmus...@globomaxnm.com On Behalf Of
Jeroen Elassaiss
multiple response model and thought that a quick way of doing this was to
grab the relative contribution from CIWRES.
Cheers
Steve
From: Jeroen Elassaiss-Schaap (PD-value)
Sent: Tuesday, 11 October 2022 8:36 am
To: Stephen Duffull
Cc: Matts Kågedal ; nmusers@globomaxnm.com
Subject: Re: [NMusers
Certara is pleased to be offering two workshops prior to the PAGE 2023 meeting
in A Coruña, Spain.
Effective Visualizations for Pharmacometrics Models (VACHETTE)
Effectively visualizing pharmacometrics models and data is crucial to inform
high-quality drug discovery and development decision
I agree. While I only met Tom in person a few times we interacted quite a bit
in my early days of PMx and NONMEM. Tom was immensely clever, kind,
unassuming, understanding and supportive. A pleasure to chat with and to learn
from.
Steve
Stephen Duffull
Senior Scientific Advisor, Certara
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