moving from animal model to the clinic
TRANSCRIPT
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Moving from Animal Model to the Clinic
Dr. Govind GiraseUDIRT, MUHS 1st Year 2012.
Saturday Club
“A Complimentary Market Research Study”
Author: Insight Pharma Reports
Publisher : Cambridge Healthtech Institute
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USE OF EXTENSIVE TECHNOLOGIES IN PHARMACEUTICAL RESEARCH
To improve operational efficacy of Drug Development
Economical pressure in drug development
To Save Drug development Time
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Risk of Administering Unsafe drug or unsafe levels of drugs in Humans
To study expected Therapeutic outcome Animal Model were Introduced
Guidelines Drafted how to Estimate safe starting Dose with respect to
(NOEL,BSA-CF, PAD,NOAEL/MTD)
Conversion of Animal Dose to Human Equivalent Dose (HED, MRSD, Safety Factor)
Allometric scaling ( Conversion Based on Body surface Area)
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From Decades of Research the Body Surface is found to be Proportional to
Blood Volume
Amount of Plasma Protein
Oxygen Utilization
Renal Function (In various Mammalian species..... )
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Conversion Of Animal dose to Human Equivalent Dose Based on Body Surface Area
Species To Convert Animal dose in mg/kg to dose in mg /m2 Multiply by km
To Convert Animal Dose in mg/kgMultiply Animal dose by
Multiply Animal Dose by
Human 37 ---- ----Human Child(20kg)
25 ---- ----
Mouse 3 12.3 0.08Hamster 5 7.4 0.13Rat 6 6.2 0.16Ferret 7 5.3 0.19Guinea pig 8 4.6 0.22Rabbit 12 3.1 0.32Dog 20 1.8 0.54Monkeys 12 3.1 0.32Squirrel Monkey 7 5.3 0.19Baboon 20 1.8 0.54Micro Pig 27 1.4 0.73Mini Pig 35 1.1 0.95
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Animal Rights Activist
Testing efficacy of a Drug candidate in more than one Animal Model
Dosing based on body surface area does not take into account the process of drug elimination
New Discoveries ( Cellular and Organismic Regulation and DNA )
“Animal Models are not very Predictive “?????
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“Animal Models are not very Predictive “
Physiology between the two species
we understand little about normal and disease biology
Uncertainties due to enhanced sensitivity to Therapeutic Activity
Difficulties in detecting certain toxicities
Unexpected toxicities
Inter Species differences in ADME of Therapeutic
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Computer Based Modelling and Stimulation Need to Develop a PK/PD Model
Physiological Biochemical Process (Metabolising Enzyme) AgeGender
Wish to get PK/PD studies done at Phase I to reduce the risk subjected to healthy volunteers
In order to get more Efficacious Exposure Allometric scaling results are compared
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Pharmacokinetic/Pharmacodynamic (PK/PD) ModellingThe Imperial method of calculating the first
in Human dose may lead to the failure of many late stage clinical trial
Companies have moved to the PK/PD Modelling with aim at predicting Dose Concentration Relationship with safety and Efficacy.
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Integrated Modelling of Biological and Pathological Processes
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Integrated Computer Modelling
HUMAN Micro-dosing
• Pk &Pd• MOA• Specific
Target
Bio-Marke
rs• Signalling Pathway
• e.g. Urinary Protein
• Drug attrition
Animal Studie
s
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Developing a PK/PD Model To Incorporated Data from Previous
Animal Studies i.e..What is Drug Target ? Agonist /Antagonist ?Is There Intra cellular Signalling?Are There Inhibition of Immunological Reaction?Are There Off Target Effects?Are There On Target adverse Effect?Clearance And BioavaibilityDrug Safety And Efficacy Biomarker ResponseDose Range
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Integrated Computer Modelling
Data used to Programme Computer
Stimulation
Biochemical Assay
Normal Biology
Disease
Cellular Regulation
Organismic Regulation
Genomics of Disease
Human Genetics
Neurobiology
Non coding DNA
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Computer Modelling and Simulation is Complementary to, but Cannot Replace,Animal StudiesPharmacokinetics
Absorption Distribution Metabolism Excretion
Pharmacodynamics Receptor Target MOA Post Receptor Effect (signal Transduction) Interaction of Drug with other Molecule
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BENEFITS Predictive models by easily incorporating proprietary
in-house data Identify potential safety risks much earlier in discovery Focus chemistry efforts on pre-clinical and clinical
safetyRescue lost investment by Identifying a new
therapeutic application for a failed development candidate
Helps to translate preclinical data into the design of human clinical trials (Micro dosing).
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PK/PD models Implemented in PharmaceuticalIndustry. Pfizer
GlaxoSmithKline
Lilly
Novartis
Entelos
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Companies Providing Developed Pk/Pd ModelsPharsight WinNonlin
(Phoenix WinNonlin Next Version Gastro Plus Announced on June 2009.)................
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Novartis has established a dedicated M&S DepartmentDr. Donald Stanski (former Vice President of Scientific
and Medical Affairs at Pharsight)
Signal transduction Pathway and Safety Modelling
Economic Modelling and Decision Analysis
e.g.. Novartis Researcher successfully completed the Modelling and Stimulation of Spinal Cord for T/t of Injuries with Monoclonal Antibodies
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Entelos focuses on building dynamic, large-scalecomputer models of human physiology and
diseaseIn silico mechanistic models of human disease
Focuses on building dynamic, large scale computer models
Facing Difficulties in signalling pathway in the body
Virtual Patient Model Diabetes Obesity Immune/Inflammatory diseases( Asthma and
Rheumatoid arthritis)
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Entelos/American Diabetes Association virtual NOD mouse modelThe design of a virtual non-obese diabetic
(NOD) mouse
multiple genetic Determinants
Components of the Immune System
Beta-cell Physiology
Pathobiology of type 1 diabetes
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References EBook Modelling and simulation approaches in drug
discovery and developmentStrategies for First to Man Studies.Pdf Adaptive Design workshop opportunities and
challenges• Pdf A dedicated SAS® Programming Group working in
a pharmaceutical Modelling & Simulation organization Pdf Novartis Accelerates Model Development Process
with Math Works Tools Ppt From Preclinical Data to Proof of Concept –