ara-toolsets>
Mark
Mark Sale M.D.
Vice President
Integrated Drug Development
mark.s...@certara.com
Remote-Forestville CA
Office Hours 9 AM - 5 PM Eastern Time
+1 302-516-1684
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Mark Sale M.D.
Vice President
Integrated Drug Development
mark.s...@certara.com
Remote-Forestville CA
Office Hours 9 AM - 5 PM Eastern Time
+1 302-516-1684
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Mark Sale M.D.
Vice President
Integrated
prohibit using PROTECT in automated
methods to run models with/without BSV, or at least makes it a little more
difficult.
Mark Sale M.D.
Vice President
Integrated Drug Development
mark.s...@certara.com
Remote-Forestville CA
Office Hours 9 AM - 5 PM Eastern Time
+1 302-516-1684
www.certara.com
-keep_tables
I'm thinking that may be easier than trying to use NWPRI.
thanks
Mark Sale M.D.
Vice President
Integrated Drug Development
mark.s...@certara.com
Remote-Forestville CA
Office Hours 9 AM – 5 PM Eastern Time
+1 302-516-1684
www.certara.com
-Original Message-
From: Heine, Rob
with the code to do this?
Thanks
Mark
Mark Sale M.D.
Vice President
Integrated Drug Development
mark.s...@certara.com
Remote-Forestville CA
Office Hours 9 AM - 5 PM Eastern Time
+1 302-516-1684
www.certara.com
This message (including any attachments) may contain confidential, proprietary
s work and a
co-investigator for this work. His laboratory has contributed sample datasets
and suggestions on the strategies for model search
Mark Sale M.D.
Vice President
Integrated Drug Development
mark.s...@certara.com
Remote-Forestville CA
Office Hours 9 AM - 5 PM Eastern Time
+1 302-51
Bill, thanks
that may be it, seems to be working, thanks
Mark
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Inc.
2525 Meridian Parkway, Suite 200
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
Upcoming Events:
Webinar:<https://www.nuventra.com/resources/eve
ase on a search for this error, it looks like it comes from dplyr. I'm running
dplyr version 0.8.4, xpose version 0.4.7 and R version 3.6.2 with R Studio,
under Windows 10.
I've tried it with and without the NOAPPEND in the $TABLE records.
Any suggestions would be appreciated.
Mark Sale M.D.
Senior V
experience trying to run v7.4,
ADVAN14 with old Intel Fortran?
thanks
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Inc.
2525 Meridian Parkway, Suite 200
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
CONFIDENTIALITY NOTICE The information in this transmittal
ies of the
transmittal.
From: Stephen Duffull
Sent: Wednesday, November 6, 2019 9:05 AM
To: Dennis Fisher ; Mark Sale
Cc: nmusers@globomaxnm.com
Subject: RE: [NMusers] Using evid 0 before dosing
WARNING: This email originated from outside of the company. Do not click links
or o
If >LLOQ has information, then !>LLOQ MUST also have information.
and Yes, we evacuated for 6 days, back home now.
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Inc.
2525 Meridian Parkway, Suite 200
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
CONFIDENT
amount of information.
That not withstanding, we also remove and pre-dose BQLs from the data set.
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Inc.
2525 Meridian Parkway, Suite 200
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
CONFIDENTIALITY NOTICE The information
e is a way to specify which mpiexec to use in a
given application, along with lots of other stuff I don't understand.
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite 200
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
Joi
MS-MPI offers several benefits:
we need to run this for another parallel application, and when we installed it,
it broke parallel NONMEM. We're using Intel Fortran, 64 bit Window Server
(2012).
thanks
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Pharma Sciences, Inc.
2525 Me
E etc. Can the SEE values in this case be
believed?
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite 200
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
/74 batch file (for deployment reasons,
would prefer not to have to edit the batch file, which would be easy enough to
do, but again, I'd like a general/deployable solution, not a custom .bat
file.). Can this be done, with the unedited version of NMFE??.bat or with PSN?
thanks
Mark Sale M.D
TO LOCAL
STARTING SUBJECTS 9 TO 17 ON MANAGER: OK
COLLECTING SUBJECTS 18 TO 32 ON WORKER2
and no mention of collecting subjects 33 to 85 on worker 3, or subjects 9 to 17
on worker 1.
so, that could be the problem.
Bob - thoughts?
Mark Sale M.D.
Senior Vice
the LRT?
But, basically, why is this happening?
thanks
Mark Sale M.D.
Senior Vice President, Pharmacometrics
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite 200
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
CONFIDENTIALITY NOTICE The information in this transmittal (including
to do it.
I'll look into the TNPRI (didn't realize that stood for triple normal, but that
makes sense).
thanks
Mark
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite 280
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com
Is it possible to use a normal prior for OMEGA? The default is inverse Wishart,
but I'd be interested in using Normal (insuring that it is positive definite)
Any ideas?
thanks
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite
thanks Bob
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite 280
Durham, NC 27713
Phone (919)-973-0383
ms...@nuventra.com<ms...@kinetigen.com>
CONFIDENTIALITY NOTICE The information in this transmittal (including
attac
pretty standard $EST I think
$ESTIMATION METH=1 NUMERICAL SLOW LAPLACIAN INTER NOTHETABOUNDTEST
NOOMEGABOUNDTEST
MAXEVAL= PRINT=1 NOABORT MSFO=MSF1
and just 1.
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite 280
, LAPLACIAN ESTIMATION METHOD MUST BE USED
It seems the Laplacian isn't used for the grid search for initial estimates
(even though specified in $EST).
any ideas?
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra Pharma Sciences, Inc.
2525 Meridian Parkway, Suite 280
Durham, NC 27713
Kudos to Jeroen, who solved this for me, needed the NOINTER option on $EST,
then you can use SAEM, which gave a reasonable answer, unlike FOCE.
Mark
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. ™
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
Office
to the apparent population in the data set.
Mark
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. ™
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
Office (919)-973-0383
ms...@nuventra.com<ms...@kinetigen.com>
www.nuventra.com<http://www.nuventra.com>
ed recipient(s). If you have received this transmittal in error,
please notify me immediately by reply email and destroy all copies of the
transmittal.
From: Bob Leary <bob.le...@certara.com>
Sent: Saturday, February 20, 2016 9:24 AM
To: Mark Sale; nmus
estimate for omega. If the data are population, and MAXE-
VALS=0 is not coded, then METHOD=1 LAPLACE is required. Compare
with PREDICTION option.
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. ™
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
O
), and it still gave me a very small difference in the
intercept for the 2nd and 3rd populations.
Is there an issue with using mixture models with logistic regression? I'm just
using FOCE, Laplacian, without interaction, and LIKE.
Any ideas?
Mark
Mark Sale M.D.
Vice President, Modeling
set, except that the limit of parallelization is the number of subjects (the
data set must be split up by subject).
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. ™
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
Office (919)-973-0383
ms...@nuventra.com
d
to learning about other peoples experience.
Mark
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. ™
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
Office (919)-973-0383
ms...@nuventra.com<ms...@kinetigen.com>
www.nuventra.com<http://www.
completely agree, no reason to use FPI,
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. ™
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
Office (919)-973-0383
ms...@nuventra.com<ms...@kinetigen.com>
www.nuventra.com<http://www.nuventra.com>
WRT bootstrap, it makes much more sense to simply bootstrap the many nonmem
runs (start 8 NONMEM runs at at time, rather than 1 run parallelized to 8
cores).
So, no, don't use parallel NONMEM for bootstrap, run multiple bootstrap samples
at the same time.
Mark
Mark Sale M.D.
Vice
ad more...<http://www.ncbi.nlm.nih.gov/pubmed/22101761>
Mark
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. ™
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
Office (919)-973-0383
ms...@nuventra.com<ms...@kinetigen.com>
www.nuventra.com<http://www
that I can't find anything about
dosing CNS drugs to peds, based on brain weight (and, ideally, brain
clearance). Does anyone know of anything?
thanks
Mark
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. (tm)
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
on tables). Tried FOCE,
IMPMAP as well as SAEM. I did try removing the offending subjects, but just
had the same problem with another (ultimately removed nearly 1/3 of the data,
still had the error). So, ended up just going back to a simpler model.
thank
Mark
Mark Sale M.D.
Vice President
assume it is crashing calculating the conditional ETAs (don't know why it
does OK in estimation). PRDERR only has the small number of error from the
estimation
Anyone seen this error, any suggestions on how to get rid of it (other than
removeing subject 51)?
Mark
Mark Sale M.D.
Vice
Li,
I'm going to go out on a limb (since I haven't seen your data or understand the
biology) and suggest that the baseline value is not a covariate, but is just
another observation (presumably with drug concentration = 0). The baseline
value is sort of by definition a function of kin. So, you
Dear Colleagues,
I'm working on a model of a malignancy that, at some point in the course of
the disease enters into an accelerated phase. I'm using a sort of standard
serial compartment model, with a zero order input rate, then first order
transit to the next compartment. I think the
?Bob,
Thanks very much, setting computers = 2 solved it
Mark
Mark Sale M.D.
Vice President, Modeling and Simulation
Nuventra, Inc. (tm)
2525 Meridian Parkway, Suite 280
Research Triangle Park, NC 27713
Office (919)-973-0383
ms...@nuventra.comms...@kinetigen.com
www.nuventra.comhttp
NREC = 10002 gives the above error.
Doesn't seem related to the size of the file, just the number of records.?
Perhaps this is related to the 4 digits assigned for the length of the data
file in FCON (but then why 10001, not 1)? Anyone know of a work-around?
thanks
Mark
Mark Sale M.D
y.com/public/systems/aSDz2458
Original Message
Subject: Re: [NMusers] Change of NSIG or R matrix
From: Ekaterina Gibiansky egibian...@quantpharm.com
Date: Wed, October 23, 2013 11:04 am
To: Mark Sale - Next Level Solutions m...@nextlevelsolns.com, nmusers
nmusers@globomax
Nick, As you point out, several (including myself) people have confirmed that the bootstrap samples that have successful covariance step do not differ from those that fail the covariance step. But that addresses the question of whether covariance is important predictor of "goodness" with the same
l consistency across different CPU types.
Best wishes,
Nick
On 13/08/2012 8:27 a.m., Mark Sale - Next Level Solutions wrote:
Martin
Yes, the results can be different. Intel has been accused of
"crippling" the executable when the Intel compiler is used on AMD CPUs
http://www.agner.o
$SIZES NO = 1000 LIM6=1000$PROBLEM large simulationdiscussed in HTML documentation under $SIZESYou may need to increase LIM6 as well as NO (number of observations)Mark Sale MDPresident, Next Level Solutions, LLCwww.NextLevelSolns.com 919-846-9185A carbon-neutral companySee our real time solar
mpartment 1, except delayed by ALAG2. PK parameters are drive only by observation in compartment 1.Mark Sale MDPresident, Next Level Solutions, LLCwww.NextLevelSolns.com 919-846-9185A carbon-neutral companySee our real time solar energy production at:http://enlighten.enphaseenergy.com/public/syst
I see another long discussion with strong feelings on both side. WRT Stu Beals comments, I had the opportunity to discuss this with him once. His point (which is to my knowledge the only argument for asuccessfulcovariance per se) is that a covariance matrix that is not positivedefinitemay
Ronald, The web site that Oskar posted seems extremely useful, and confirmed the rumors that have been around for awhile. But, I'm wondering why anyone would use 32 bit, when 64 bit is faster (about 20%) and seems to be better behaved numerically?MarkMark Sale MDPresident, Next Level Solutions,
Inhibitors Using Statistical Response-Surface Modelling by Clare S
Gavigan, Stella G Machado, John P Dalton, Angus Bell
Antimicrobial Agents and Chemotherapy (2001)
Volume: 45, Issue: 11, Publisher: American Society for Microbiology,
Pages: 3175-3181
Mark Sale MD
President, Next Level Solutions
Yuhong, You likely have a predicted value of 0 at some point (maybe a predose sample?). With a predicted value of 0, the proportional error variance will be 0, and you have the additive error variance fixed to 0. So, the total error variance will be zero. Since the "weight" for the sum of squares
. . . 1 ; this is the observation, recorded at 1 hour, but is at unknown time
2. . . 2 ; this is the observation, recorded at 2 hours, and really is3. . . 2 ; this is the observation, recorded at 3 hours, and really is
$PKALAG1 = THETA(1)ALAG2 = 0K10 = THETA(2)K20 = THETA(2)Mark Sale
Nick,I'm a little surprised at your choice of benchmarks for parallel NONMEM. The original motivation for this was a run that was taking 2 to 3 weeks, and we thought it would be nice we could get that down to 2 or 3 days (best we had at the time was an 8 processor server). You are correct, if
GPU was considered in the work leading up to the upcoming parallel NONMEM. GPU computing is intended essentially for very simple algorithms applied to a large number of very similar data sets (things like bit shifting everything left, or adding a number to every value of a matrix). Really not
I wasn't aware that there was a 12 core Intel CPU - maybe you have a dual processor 6 core? If you have a 12 core AMD CPU, you should be aware that this only has 6 floating point cores. In addition, if you use the Intel compiler with AMD CPUs, Intel cleverly disables all optimization, so the CPU
Georgios The most straightforward way (and the only way I know of) to do this is to call an external fortran subroutine. Pretty easy to call it (just include it in the $SUBS). I've never done a real analytical solution (like root finding or something), but I've done simple search algorithms. I'm
Ann, We benchmarked 32 bit vs 64 bit Intel fortran with NONMEM a few years ago, with 64 bit XP - the 64 bit version was 10-20% faster.NONMEM does not multithread (although the next version will multi process). IMHO, you get the most for your money with an quad core Intel i5, it is essentially as
, 2011 12:07 pm
To: Mark Sale - Next Level Solutions m...@nextlevelsolns.com
Cc: Ann Rigby-Jones ann.rigby-jo...@pms.ac.uk,
"nmusers@globomaxnm.com" nmusers@globomaxnm.com
Ann,
RAM could be a problem if you like to run 16 jobs at once. If so, you
may need a 64-bit machine to support more
Title: Block versus diagonal omega
Brian, Let me risk ridicule and mention my favorite algorithm, Genetic algorithm. We've actually done some work in this area (just a little, not published anything). But, it is pretty easy to set up an optimization with constraints. Basically, you simulate
, put them in if you can. I do find that including them can greatly reduce residual (intra individual) variance, but that commonly the VPC bands are wider (making NPC, NPDE and PPC easier to pass, a side benefit).Mark Sale MDNext Level Solutions, LLCwww.NextLevelSolns.com 919-846-9185A carbon-neutral
Sam, Many years ago Stuart scolded me for using the Unconditional option, saying that a model that didn't converge had no chance of a successful covariance step (I didn't ask why he put the option in if he didn't want people using it). But, I have had put a couple of models that appeared to be
Joachim et al. Moreover, assays are typically done in duplicate or triplicate, with only the mean reported. We had many discussions at GSK with the chemists about getting "all" the data (BQL, all replicates) promising everything imaginable (first, the data would never end up in a regulatory
Title: Coding a triple absorption model
Mahesh, Consider modeling F2 as a fraction of the part of bioavailablilty left over after F1:LF1 = THETA(1)*EXP(ETA(1))F1= LF1/(1+LF1) LF2 = THETA(2)*EXP(ETA(2)) F2 = (1-F1)*(LF2/(1+LF2)) ;LF2 DESCRIBES FRACTION OF THE STILL AVAILABLE DOSE (1-F1)F3 =
s a successful covariance step - of course everything else is never equal).Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: RE: [NMusers] OMEGA selection
From: "Hang, Yaming" yaming_h...@merck.com
Date: Thu, April 23, 2
, a VPN accross the internet. Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: [NMusers] NONMEM with ACCELLERANT
From: Santosh santosh2...@gmail.com
Date: Tue, April 21, 2009 4:20 pm
To: nmusers@globomaxnm.com
Dear NM users,Some time
Guess I didn't actually answer your question. To my knowledge, ACCELERANT for NONMEM was never run on a cluster, only on a multi processor server. I'm only familiar with GSK's and ASPEED internal experience.Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Nick et al. At this risk of starting an discussion that probably has little mileage left in it. First I agree with Nick on covariance - it probably doesn't matter. But, I'd like to point out what may be an error in our logic. We content that we have demonstrated that covariance doesn't matter.
Section II, V.A, V.IREFERENCES: Guide IV Section V.B, V.C.5 Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: [NMusers] 20 variable limit in $INPUT
From: andreas.kra...@actelion.com
Date: Mon, March 16, 2009 9:43 am
To: nmusers
Leonid et al, I'm a little confused by this discussion. To make an analogy, assume that drug company A has a wonderful theory that drug B will treat a disease. Theory makes sense by your favorite epistemology criteria etc. But of course, being good scientists, we know that theories must be
Background, Most modern computers use a system called ECC (Error checking/correction) wherein each memory location has an extra bit (the parity bit) that is used for checking whether the data location is "correct". Interestingly, data bits in memory can actually change randomly, due to electro
Kyun-Seopsee:http://www.ecpag.org/presentations/2006/0725/5_MarkSale.pdfMarkMark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: [NMusers] What would the impact be, if NONMEM runs 10 times
faster than now?
From: "BAE, KYUN-SEOP"
Does anyone have a reference to a publication assessing whether mixed effect modeling (NONMEM in particular) is robust for unbalances studies? I see if in a number of courses (including the original beginners course for NONMEM), but can't find a publication.thanksMark Sale MDNext Level Solutions,
Hong-GuangAnalyses across so many studies are notoriously difficult, especially with different routes of administration. My personal experience is that the most common cause for this sort of thing is errors in the data set.Make sure that the dose and concentration units are the same for all
is 0, no change is made in the status of any compart- ment. PCMT is the same as for dose events.Mark (aka Golum)Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: [NMusers] How to code vomit event as absorption lag and lost
have multiple emesis events.Mark Mark Sale MD Next Level Solutions, LLC www.NextLevelSolns.com 919-846-9185 Original Message Subject: [NMusers] How to code vomit event as absorption lag and lost of amount in administration comp. From: Galadriel [EMAIL PROTECTED] Date: Tue, July
Saik, Thanks for your views on this - are there some simulation results that you've seen, or other basis for the limit of 2-3? Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: Re: [NMusers] algorithm limits
From
MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: Re: [NMusers] algorithm limits
From: Leonid Gibiansky [EMAIL PROTECTED]
Date: Sat, July 19, 2008 5:36 pm
To: Mark Sale - Next Level Solutions [EMAIL PROTECTED]
Cc: nmusers@globomaxnm.com
Hi
: Sat, July 19, 2008 9:37 pm
To: Mark Sale - Next Level Solutions [EMAIL PROTECTED]
Cc: nmusers@globomaxnm.com
Mark,
The description that you gave confirms that population model has limited
value unless four parameters (baseline, percent change, time to drop and
time to recovery) correlate somehow
t gets a little more complicated.you can put whatever you want into it, it will be save between calls to DES, and it available in $PK and $ERROR (you'll need to put in the same COMMON statements in $PK or $ERROR).Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
-
Dear Colleagues,Next Level Solutions will be presenting a seminar titled"General approach to population pk/pd model selection, opportunity for improvement?"at the Indiana University/Purdue University Clinical Pharmacology Division in Indianapolis on May 27thcontact me or Dave Flockhart ([EMAIL
Carlos, I don't have any references for drudevo other than their website,Here is a reference for my workhttp://www.springerlink.com/content/m7757p17u5058887/and here is one for Ken Kowalski's paperhttp://www.springerlink.com/content/r20052w42710217k/Kens program, last I checked, ran from SAS.and
Carlos I'm not sure what you want to do. DruDevo (www.drudevo.com, don't know if they are still around) has a web site that seems to imply they do some of this:
Automated structural
model search
Automated statistical
model search
Automated multi level
covariate search
Automated multi level
Rik,I don't know anything about the non-parametric estimates: 'expected value of ETA' and
'Covariance matrix of ETAI. But, think the correlation matrix is CORRM in COMMON /CM12/ COVM(LPAR3),COVINM(LPAR3),STHTA(LTH),SEN(LVR,LVR), 1 CORRM(LPAR3),NVLS,VLS(LPAR)and you can get at it something like
Jin, Another options it the Fortran app nmsee (ftp://ftp.globomaxnm.com/Public/nonmem/nmsee/)or a version of nmsee I recently put together (cleverly called nmsee2) at http://www.nextlevelsolns.com/downloads.html. These are both post-processors that read the NONMEM output file (and so you only get
I'm thinking of doing a somewhat formal analysis of the meaning of a failed covariance step. Some years ago Stu Beal explained that (as I recall), if the covariance step fails you cannot be sure that the minimum isn't a saddle point, which makes sense to me, and is consistent (I think), with the
you explain that the same models reformulated with ANDAN6 run? Well, they take very long... and none of them has run to a successful minimization yet. JoachimMark Sale - Next Level Solutions [EMAIL PROTECTED] 07.12.2007 13:44 <tr!
valign="top"> To [EMAIL PROTECT
these file. It doesn't (usually) happen with the original data set, unless you try to run NMTRAN simultaneously. Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
919-846-9185
Original Message
Subject: RE: [NMusers] error (157) forrtl: severe
From: "Brian M. S
I think I recently saw a thread about this, but is there a way to fix the bug/feature where NONMEM v6 gives this message:0THE SIMULATION TASK REQUIRES THAT A BETTER FINAL ESTIMATEBE AVAILABLE IN THE MODEL SPECIFICATION FILEand will do a simulation with an MSF regardless?thanksMarkMark Sale MD
PROTECTED]
Date: Fri, October 26, 2007 2:56 pm
To: "'James G Wright'" [EMAIL PROTECTED], "'Mark Sale - Next
Level Solutions'" [EMAIL PROTECTED]
Cc: "'nmusers'" nmusers@globomaxnm.com
James, Mark
I don't have time to go through all RCTs in this manner.
But I wil
modeling to select dosing regimens, and finish with a purely regulatory and marketing piece of work that I'm familiar with:http://www.aesnet.org/Visitors/AnnualMeeting/A!
bstracts/dsp_Abstract.cfm?id=2578(this got published as a real article, but I can't find a link to the paper).Mark Sale MD
Next Level
Original Message
Subject: RE: [NMusers] Reporting Modeling Results
From: "Stephen Duffull" [EMAIL PROTECTED]
Date: Thu, October 25, 2007 6:52 pm
To: "'Mark Sale - Next Level Solutions'" [EMAIL PROTECTED]
Cc: "'nmusers'" nmusers@globomaxnm.com
Mark, Nick
Sam,I think you should have gotten the error:INITIAL ESTIMATE OF OMEGA HAS A NONZERO BLOCK WHICH IS NUMERICALLY NOT POSITIVE DEFINITEwhich is the case. (you can check this in Excel, using the MDETERM function, the determinant is -2945). When you get this message, try reducing the off-diagonal
Dear Colleagues,The windows based NONMEM output viewer described earlier has been updated, with bug fixes. Bug fixes are that it now correctly handles SAME blocks and handles missing files and files that are not NONMEM output files correctly. Additional features include printing out SE of
, Cmax, Cmin) and some measure of variability (SE of AUC
etc), since an artificially large variability can fool PPC.
Mark Sale MDNext Level Solutions, LLCwww.NextLevelSolns.com
Original Message
Subject: Re: [NMusers] Minimization terminated ?
From: Nick Holford [EMAIL PROTECTED]
Da
.TXT, from the NONMEM home directory.The Introduction to NONMEM VI does alert the user that there are newerror messages but does not provide the details. This response will becopied to nmusers so that users are better informed.Thank you for your message.Tom Ludden Mark Sale MDNext Level
Dear Colleagues, I've created a Windows application for summarizing NONMEM output file, called nmsee2 (after the original NMSEE). I've put the setup files on the Next Level Solutions web site (http://www.nextlevelsolns.com/downloads.html, near the bottom). This application was written to extract
number is available in PK, but you
have it in this file with the standard NONMEM output.
Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
Original Message
Subject: [NMusers] How to generate an output file with individual
parameters at each iteration
From: Benjamin
of that range again)?
Mark
Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
Original Message
Subject: Re: [NMusers] NONMEM ODE solver
From: Alison Boeckmann [EMAIL PROTECTED]
Date: Mon, May 28, 2007 1:01 pm
To: Benjamin Ribba [EMAIL PROTECTED],
nmusers
-dosing drugs, and estimated the resulting fatalities. Making
dosing more complicated is unlikely the help. In addition, each
company very much wants their drug to be simpler to use than their
competitors.
Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
Original Message
from the last subject.
This is all OK for the minimization, you just need to be aware of it
when interpreting output, plots, tables etc. that the first value for
CONC for a subject will not be correct.
Mark
Mark Sale MD
Next Level Solutions, LLC
www.NextLevelSolns.com
Original Message
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