Dear All,


Pharmacometrica will be holding an advanced course on pharmacometrics at the
Chateau de Longcol (France):



Advanced course on Pharmacometrics

30 March - 2 April 2015

Château de Longcol, Longcol, La Fouillade (France)



Course outline

Develop and implement a pharmacometric and optimal study design strategies:

a) To evaluate the relationship between the exposure of an active drugs
(methylphenidate-MPH) and the clinical response in presence of placebo
effect for the treatment of the Attention Deficit/Hyperactivity Disorder
(ADHD) disease in children,

b)         To determine the relationship between the drug delivery and the
clinical response,

c) To determine the optimal study design in a pediatric population for
evaluating new formulations of MPH.



MPH is a CNS stimulant that is thought to block the reuptake of dopamine and
noradrenaline (norepinephrine) into the presynaptic neuron. A sustained
release (OROS formulation) of the drug has been developed for use in
children with ADHD. The OROS delivery technology provides a mixture of
immediate and delayed release. Within 1 hour, plasma MPH concentrations
reach an initial plateau, followed by a gradual increase over the next 5 to
9 hours. The behavioral manifestations of ADHD during analog classroom
sessions following placebo of MPH treatment will be determined using the
longitudinal changes in the SKAMP Rating Scale.



Course objectives

·    To develop a population PK model for describing the complex absorption
profile of an  OROS formulation of MPH

·    To develop a placebo response model in children with ADHD

·    To develop an indirect-response model to jointly evaluate the placebo
and drug relate response

·    To evaluate the relative impact of the immediate and the delayed
release of MPH   (administered using the OROS formulation) on the
therapeutic response

·    To determine the optimal study design in pediatric population for
assessing the   performances of novel formulations of MPH.



Topics include

·    Methods for digitalizing images and for generate working data (PK,
placebo, PD) by extracting data from selected publications

·    Placebo response and drug action model development

·    Indirect model PKPD model development for jointly analyze placebo and
MPH related response

·    Evaluation of alternative models for describing complex absorption PK
profiles

·    Evaluation of alternative models for describing the placebo and the MPH
response

·    Implementation of an R based simulator for generating virtual data
describing the population PK and clinical responses (placebo and drug
related)

·    Optimization of the study design in pediatric population using optimal
design methods

·    Implementation of the overall pharmacometrics projects using a
pipelining workflow solution using a visual graphical GUI and R as task
definition language.



Additional details are available at:
<http://pharmacometricaworkshop.webs.com/>
http://pharmacometricaworkshop.webs.com/







Roberto Gomeni, PhD, HDR, Adjunct Professor at UNC

Pharmacometrica

Longcol, 12270 La Fouillade (France)

E-mail:  <mailto:[email protected]>
[email protected]

 <http://www.pharmacometrica.com/> www.pharmacometrica.com

Next workshops on pharmacometrics:
<http://pharmacometricaworkshop.webs.com/>
http://pharmacometricaworkshop.webs.com/





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L'absence de virus dans ce courrier électronique a été vérifiée par le logiciel 
antivirus Avast.
http://www.avast.com

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