modeling and simulation in drug development presented to the pharmaceutical sciences advisory...
TRANSCRIPT
![Page 1: Modeling and Simulation in Drug Development Presented to the Pharmaceutical Sciences Advisory Committee Michael D. Hale, Ph.D. Glaxo Wellcome November](https://reader035.vdocuments.mx/reader035/viewer/2022062423/5697c00b1a28abf838cc84d8/html5/thumbnails/1.jpg)
Modeling and Simulationin
Drug Development
Presented to the
Pharmaceutical Sciences Advisory Committee
Michael D. Hale, Ph.D.
Glaxo Wellcome
November 16, 2000
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Knowledge Generation Cycle
Experiment Experiment Observe Observe Collect Data Collect Data
SummarizeSummarizeAnalyzeAnalyzeInterpretInterpret
ModelModelSimulateSimulatePredictPredict
PharmaceuticalCompaniesDo These
PharmaceuticalCompaniesDo These
FDA Reviews,Evaluates,
Approves orRejects
FDA Reviews,Evaluates,
Approves orRejects
The Grey Zone:Used mostly bypharmaceuticalcompanies forinternal decisions
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Modeling & Simulation
• Modeling and Simulation are a technical articulation of our understanding (current state of knowledge; beliefs; accepted science)
Within the context of our science / premises,
• Modeling is the framework / rationale for explaining existing data
• Simulation expresses our expectation of behavior where data are lacking (or sparse)
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Why Modeling & Simulation?
We believe they enable us to provide
• improved patient therapy– greater beneficial effect– better safety– dosing convenience & “robustness”
• more effective and efficient use of limited resources– reduce costs of producing innovative medicines– faster product introduction without compromise
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Part I
Modeling & Simulation
in
Drug Development
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Primary Areas of Use
• Pre- and Non-Clinical
• First time in Humans
• “Specialty” studies
• Proof of Concept
• Phase III
• Post Marketing
Basically, we use it about everywhere!
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Pre-Clinical & Non-Clinical
• blood clotting cascade model
• receptor-ligand-inhibitor interactions
• receptor multimeric state models
• viral resistance emergence• ADME
– library design– selection for in-vitro, in-vivo
testing or screening– property/physiochemical
relationships
• E. coli strain optimization• process capability /
product specifications• product quality (process
Vs product characteristics)• stability• analytical method
development
Note: usually considered Private and Proprietary, with notable exceptions
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Molecular Descriptorse.g.size, charge, lipophilicity, hydrogen bonding, fragments, fingerprints
ADME Datae.g Pharmacokinetics, Absorption, Metabolism, Brain Penetration etc
BUILD ADME MODELS
Statistical & Mathematical e.g. Multiple linear regression,principal component and cluster analysis, cellular automata, calculus, decision trees
CHEMISTS / DRUG DISCOVERY PROJECTSLibrary Design/Understand Physchem Relationships etc
Information
GlobalDatabase
ADME In-silico Modelling Process
Thanks to Anne Hersey & team for this slide!
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“Early” Clinical Development
• Selecting drug dose– amount– frequency
• PK sampling schedule
• Expected beneficial effect & safety*
• Comparison with competitors (internal and external)
*Note: safety is generally much more difficult to model, as an “all comers” situation, whereas effectiveness is targeted & better defined
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Basic Concept: A Sample “Chaining” of Models
D oseD rugC onc
B ioM arker1
B ioM arker2
C lin ica lR esponse
M arketValue
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Example: Concentration/Safety Relationship Early Evaluation
1 10 100 1000
0.8
1.0
1.2
1.4
1.6
1.8
2.0
2.2
2.4
2.6
2.8
3.0
3.2
3.4
Observed dose1 in man
Observed dose2 in man
Modeled effectcurve in man(previouslystudied drug)
Simulated effect curvein man from rat model(candidate drug)
Sa
fety
ma
rke
r
Conc (ng/mL)
Thanks to Misba Beerahee & team for this slide!
Undesirable Effect Level
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Evaluation of Dose & Drug t1/2 for Effect
10 100 1000
0
20
40
60
80
100
Simulated Dose-Response curves for a drug attwo possible elimination half-lives in man
6h half-life12h half-life
% o
f Max
incr
ease
in E
ffect
Daily Drug dose (mg)
Thanks to Paul Mudd & team for this slide!
t1/2 impact
dose impact
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“Late” Clinical Development
• Dose optimization
• Extension to other populations
• Alternative dosing regimens
• Optimal times and measures for evaluation
• Individualization of therapy?
• Examination of statistical tests (particularly in complex situations)
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Example: Simulation comparing therapeutic drug monitoring with fixed dosing
Simulation indicated proportion of patients benefiting from TDM, and degree of benefit
(unpublished, done to support investigator trial)
Individual Patient Benefit via Hale TDMAlgorithm Compared to Fixed Dose
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
0% 10% 20% 30% 40% 50% 60% 70% 80%
Patient at Population Percentile for AUC
% R
isk
Re
du
cti
on
Algorithm
Fixed
Action Limits at 20%, 40%, 85%, 95%
Pro
bab
ilit
y o
f B
enef
icia
l E
ffe
ct
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Part II
Why Might a Rational Person
be Skeptical About
Modeling and Simulation?
Issues, and a way forward...
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Why Not Simulate?
Three legitimate reasons to challenge a modeling and simulation project
• Assumptions (Premises)
• Implementation
• Interpretation
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Premises (Two Classes)
Verifiable
• Accepted theory & models
• Supporting data
• Compelling plausibility
Subject of a Simulation Study
• Study “factor”
• “Noise”
ExpertsAgree
ExpertsDisagree
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Premises (Two Classes)
Verifiable
• Accepted theory & models
• Supporting data
• Compelling plausibility
Subject of a Simulation Study
• Study “factor”
• “Noise”Migrate on Disagreement
MoreCertain
LessCertain
Gain Expert Agreement with more Data, Knowledge, Advancement of Science,
Experience, etc.
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Implementation
Primary Question:
Do the modeling & simulation plan and software faithfully embody the premises?
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Towards Confidence in Implementation
General Framework• “Standard” accepted
tools• Validated model
libraries• Traditional software
validation• Benchmark case
studies
Specific Application• Credibility of
implementers• Independent review
– peer presentation– 3rd party?– line-by-line?
i.e., was “validated” system used properly?
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Interpretation
• Requires collaboration of subject matter and statistical expertise (& simulation expertise?)
• Relevance
• Scope
• Interpolation or extrapolation?
• Precedence
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Summary: Why Not Simulate?
Legitimate reasons to challenge a modeling and simulation project
• Assumptions (Premises)
• Implementation
• Interpretation
Hale Claims:
– Manageable. Negotiate shareholder agreement“up front”. *Excessive rigor could dilute value
– Achievable, with intensive ongoing effort (standardized libraries will help)
– Perhaps no more difficult than interpretingclinical trials?
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Part III
Published Perspectives
on
Modeling & Simulation
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Recent Clinical References
• Review “Simulation of Clinical Trials” – Holford, Kimko, Monteleone, & Peck in Ann. Rev.
Pharmacol. Toxicol 2000. 40:209-34
• Review “PK/PD Modeling in Drug Development” – Sheiner and Steimer in Ann. Rev. Pharmacol. Toxicol
2000. 40:67-95
• July 25, 2000 FDA Antiviral AC on PK/PD– see http://www.fda.gov/ohrms/dockets/ac/cder00.htm#Anti-Viral
• “Good Practices” conference & consensus paper – see http://www.dml.georgetown.edu/cdds/sddgp723.html
• FDA Guidance on Population Pharmacokinetics
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Relevant (?) FDA Guidance
The May 1998 “Providing Clinical Evidence of Effectiveness for Human Drug and Biological Products” has goals
– “to articulate its current thinking concerning the quantitative and qualitative standards for demonstrating effectiveness of drugs and biologics.”
– “to encourage the submission of supplemental applications to add new uses to the labeling of approved drugs.”
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Effectiveness Guidance, pt 2
• “Section 1 addresses situations in which effectiveness of a new use may be extrapolated entirely from existing efficacy studies.”
• “In certain cases, effectiveness of an approved drug product for a new indication, or effectiveness of a new product, may be adequately demonstrated without additional adequate and well-controlled clinical efficacy trials. Ordinarily, this will be because other types of data provide a way to apply the known effectiveness to a new population or a different dose, regimen or dosage form.”
• Examples: pediatric, bioequivalence, modified-release dosage forms, different doses, regimens, or dosage forms
Emphasis is mine
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Do we currently combine premise, data, & analysis for regulatory approval?
• Premise (“equivalent rate & extent” equivalent drug)
plus• Data
(one pharmacokinetic clinical trial)
plus• Statistical analysis
(including decision criteria)
Conclusion equivalent effect & safety(without clinical testing of safety & effectiveness)
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Conclusions
• Modeling and simulation are a natural and necessary part of advancing the scientific understanding of drug characteristics
• Many early uses will be private and proprietary (i.e., perceived as providing competitive advantage, without any effect on patient safety or beneficial effect)
• Combining premise, data, and analysis for agreed conclusions is not new