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Population PK/PD — Nonlinear Mixed Effects Modeling Training | PopPK Concepts, NLME & Dosing

NTHRYS >> Services >> Academic Services >> Training Programs >> Bioinformatics Training >> Pharmacogenomics, Pharmacometrics & Precision Therapeutics >> Population PK/PD — Nonlinear Mixed Effects Modeling Training | PopPK Concepts, NLME & Dosing

Population PK/PD — Nonlinear Mixed Effects Modeling — Hands-on

Build a strong conceptual foundation in population pharmacokinetics and pharmacodynamics (PopPK–PD) using nonlinear mixed-effects (NLME) thinking. You will learn how to frame PopPK–PD questions, interpret model parameters and variability, explore covariate effects and simulate dosing scenarios to support model informed drug development and precision therapy.

Population PK/PD — Nonlinear Mixed Effects Modeling
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Session 1
Fee: Rs 8800
PopPK/PD Concepts & Study Designs
  • Why population PK/PD? Questions PopPK models can address
  • between patient variability exposure response themes dosing in special populations
  • PopPK/PD vs classical PK — conceptual differences
  • individual vs population focus fixed vs random effects thinking handling sparse sampling
  • Study designs for PopPK/PD data collection (conceptual)
  • intensive vs sparse designs rich and opportunistic sampling linking design to model goals
Session 2
Fee: Rs 11800
NLME Parameters, Variability & Error
  • Structural model concepts (one/two compartment, PD effect)
  • absorption and distribution ideas clearance and volume thinking direct and indirect PD responses
  • Random effects and variability components (conceptual)
  • between subject variability residual unexplained variability inter occasion variability themes
  • Error models and data characteristics
  • additive vs proportional error ideas log transformed data intuition linking error choice to data range
Session 3
Fee: Rs 14800
Covariates, Diagnostics & Simulations
  • Concepts for covariate screening and selection
  • continuous vs categorical covariates clinical plausibility first parsimony and overfitting concerns
  • Diagnostic plot themes for PopPK–PD models
  • observed vs population/individual predictions residuals vs time and predictions visual predictive check ideas
  • Simulating dosing regimens and clinical scenarios
  • typical vs extreme patients dose and interval exploration exposure and response bands
Session 4
Fee: Rs 18800
Mini Capstone: PopPK–PD Case & Dosing
  • Select a PopPK–PD example and summarize model insights
  • describe structural model and parameters summarize variability and covariate effects highlight key exposure response findings
  • Translate PopPK–PD results into practical dosing guidance
  • dose bands for typical and high risk groups monitoring and safety considerations scenarios for future data collection
  • Deliverables: PopPK–PD case slide deck and one page summary
  • PDF or PPTX ready for MIDD or PMx meetings template for future PopPK projects


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