Andrew Hooker
Professor at Department of Pharmacy; Pharmacometrics
- Mobile phone:
- +46 70 167 90 48
- E-mail:
- andrew.hooker@uu.se
- Visiting address:
- Biomedicinskt Centrum BMC, Husargatan 3
- Postal address:
- Box 580
751 23 UPPSALA
Download contact information for Andrew Hooker at Department of Pharmacy; Pharmacometrics
- ORCID:
- 0000-0002-2676-5912
Short presentation
My research is focused on pharmacometrics (PKPD). Topics include optimal experimental design, methodological problems associated with building and evaluating PKPD models, modeling discrete data, and the development and use of PKPD models in a range of therapeutic areas and drug classes including cancer, addiction, PET, progressive disorders, and biologics. I also develop a number of software programs for pharmacometrics.
I teach courses in statistics, drug development, and pharmacometrics.
Keywords
- free and open source software
- pharmacometrics
- pkpd
- optimal experimental design
- optimal design
- population models
- nonlinear mixed-effects models

Publications
Selection of publications
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The Role of Model Master Files for Sharing, Acceptance, and Communication with FDA
Part of AAPS Journal, 2024
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Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
Part of Orphanet Journal of Rare Diseases, 2023
- DOI for Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
- Download full text (pdf) of Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
-
Part of CPT, p. 624-630, 2023
- DOI for Establishing the suitability of model-integrated evidence to demonstrate bioequivalence for long-acting injectable and implantable drug products: Summary of workshop
- Download full text (pdf) of Establishing the suitability of model-integrated evidence to demonstrate bioequivalence for long-acting injectable and implantable drug products: Summary of workshop
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Part of AAPS Journal, 2021
- DOI for Bounded Integer Modeling of Symptom Scales Specific to Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia
- Download full text (pdf) of Bounded Integer Modeling of Symptom Scales Specific to Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia
-
Pharmacometrics meets statistics-A synergy for modern drug development
Part of CPT, p. 1134-1149, 2021
- DOI for Pharmacometrics meets statistics-A synergy for modern drug development
- Download full text (pdf) of Pharmacometrics meets statistics-A synergy for modern drug development
-
Metaheuristics for pharmacometrics
Part of CPT, p. 1297-1309, 2021
- DOI for Metaheuristics for pharmacometrics
- Download full text (pdf) of Metaheuristics for pharmacometrics
-
Tutorial for $DESIGN in NONMEM: Clinical trial evaluation and optimization
Part of CPT, p. 1452-1465, 2021
- DOI for Tutorial for $DESIGN in NONMEM: Clinical trial evaluation and optimization
- Download full text (pdf) of Tutorial for $DESIGN in NONMEM: Clinical trial evaluation and optimization
-
Part of Clinical Pharmacology and Therapeutics, p. 1190-1195, 2021
- DOI for Public Workshop Summary Report on Fiscal Year 2021 Generic Drug Regulatory Science Initiatives: Data Analysis and Model-Based Bioequivalence.
- Download full text (pdf) of Public Workshop Summary Report on Fiscal Year 2021 Generic Drug Regulatory Science Initiatives: Data Analysis and Model-Based Bioequivalence.
-
Part of Clinical Pharmacology in Drug Development, p. 220-228, 2021
-
Part of AAPS Journal, 2020
- DOI for Item Response Theory Modeling of the International Prostate Symptom Score in Patients with Lower Urinary Tract Symptoms Associated with Benign Prostatic Hyperplasia
- Download full text (pdf) of Item Response Theory Modeling of the International Prostate Symptom Score in Patients with Lower Urinary Tract Symptoms Associated with Benign Prostatic Hyperplasia
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Population Pharmacokinetics and Dosing of Ethionamide in Children with Tuberculosis
Part of Antimicrobial Agents and Chemotherapy, 2020
-
Part of AAPS Journal, 2020
- DOI for Saddle-Reset for Robust Parameter Estimation and Identifiability Analysis of Nonlinear Mixed Effects Models
- Download full text (pdf) of Saddle-Reset for Robust Parameter Estimation and Identifiability Analysis of Nonlinear Mixed Effects Models
-
Optimizing Dose-Finding Studies for Drug Combinations Based on Exposure-Response Models
Part of AAPS Journal, 2019
-
Feasibility of Exposure-Response Analyses for Clinical Dose-Ranging Studies of Drug Combinations
Part of AAPS Journal, 2018
-
Adaptive Optimal Designs for Dose-Finding Studies with Time-to-Event Outcomes
Part of AAPS Journal, 2018
- DOI for Adaptive Optimal Designs for Dose-Finding Studies with Time-to-Event Outcomes
- Download full text (pdf) of Adaptive Optimal Designs for Dose-Finding Studies with Time-to-Event Outcomes
-
A Population Pharmacokinetic-Pharmacodynamic Model of Pegfilgrastim
Part of AAPS Journal, 2018
- DOI for A Population Pharmacokinetic-Pharmacodynamic Model of Pegfilgrastim
- Download full text (pdf) of A Population Pharmacokinetic-Pharmacodynamic Model of Pegfilgrastim
-
Part of AAPS Journal, 2018
- DOI for Implementing Optimal Designs for Dose-Response Studies Through Adaptive Randomization for a Small Population Group
- Download full text (pdf) of Implementing Optimal Designs for Dose-Response Studies Through Adaptive Randomization for a Small Population Group
-
Part of AAPS Journal, 2018
- DOI for Model-Based Adaptive Optimal Design (MBAOD) Improves Combination Dose Finding Designs: an Example in Oncology
- Download full text (pdf) of Model-Based Adaptive Optimal Design (MBAOD) Improves Combination Dose Finding Designs: an Example in Oncology
-
Reduced and optimized trial designs for drugs described by a target mediated drug disposition model
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 637-647, 2018
- DOI for Reduced and optimized trial designs for drugs described by a target mediated drug disposition model
- Download full text (pdf) of Reduced and optimized trial designs for drugs described by a target mediated drug disposition model
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Model-Informed Drug Development and Review for Generic Products: Summary Of FDA Public Workshop
Part of Clinical Pharmacology and Therapeutics, p. 27-30, 2018
-
Part of CPT, p. 418-429, 2017
-
Model Evaluation of Continuous Data Pharmacometric Models: Metrics and Graphics
Part of CPT, p. 87-109, 2017
- DOI for Model Evaluation of Continuous Data Pharmacometric Models: Metrics and Graphics
- Download full text (pdf) of Model Evaluation of Continuous Data Pharmacometric Models: Metrics and Graphics
-
Assessing robustness of designs for random effects parameters for nonlinear mixed-effects models
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 611-616, 2017
-
Model selection and averaging of nonlinear mixed-effect models for robust phase III dose selection
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 581-597, 2017
- DOI for Model selection and averaging of nonlinear mixed-effect models for robust phase III dose selection
- Download full text (pdf) of Model selection and averaging of nonlinear mixed-effect models for robust phase III dose selection
-
The effect of using a robust optimality criterion in model based adaptive optimization.
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 317-324, 2017
- DOI for The effect of using a robust optimality criterion in model based adaptive optimization.
- Download full text (pdf) of The effect of using a robust optimality criterion in model based adaptive optimization.
-
Part of AAPS Journal, p. 505-518, 2016
-
Accelerating Monte Carlo power studies through parametric power estimation
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 223-234, 2016
- DOI for Accelerating Monte Carlo power studies through parametric power estimation
- Download full text (pdf) of Accelerating Monte Carlo power studies through parametric power estimation
-
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 211-224, 2015
-
Part of British Journal of Clinical Pharmacology, p. 6-17, 2015
-
Optimal clinical trial design based on a dichotomous Markov-chain mixed-effect sleep model
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 639-654, 2014
- DOI for Optimal clinical trial design based on a dichotomous Markov-chain mixed-effect sleep model
- Download full text (pdf) of Optimal clinical trial design based on a dichotomous Markov-chain mixed-effect sleep model
-
Part of Pharmaceutical research, p. 2152-2165, 2014
- DOI for Improved Utilization of ADAS-cog Assessment Data through Item Response Theory based Pharmacometric Modeling
- Download full text (pdf) of Improved Utilization of ADAS-cog Assessment Data through Item Response Theory based Pharmacometric Modeling
-
Modeling and Simulation Workbench for NONMEM: Tutorial on Pirana, PsN, and Xpose
Part of CPT, 2013
-
PopED: An extended, parallelized, nonlinear mixed effects models optimal design tool
Part of Computer Methods and Programs in Biomedicine, p. 789-805, 2012
-
Prediction-Corrected Visual Predictive Checks for Diagnosing Nonlinear Mixed-Effects Models
Part of AAPS Journal, p. 143-151, 2011
-
Optimal Design in Population Kinetic Experiments by Set-Valued Methods
Part of AAPS Journal, p. 495-507, 2011
-
Adaptive-Optimal Design in PET Occupancy Studies
Part of Clinical Pharmacology and Therapeutics, p. 563-571, 2010
-
Conditional weighted residuals (CWRES): a model diagnostic for the FOCE method
Part of Pharmaceutical research, p. 2187-2197, 2007
-
Simultaneous population optimal design for pharmacokinetic-pharmacodynamic experiments.
Part of AAPS Journal, 2005
-
Robust population pharmacokinetic experiment design.
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 33-64, 2005
Recent publications
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Part of CPT, 2026
- DOI for Optimizing Clinical Study Designs for CAR-T Cell Therapy: Development of an Efficient Sampling Strategy Through Optimal Experimental Design
- Download full text (pdf) of Optimizing Clinical Study Designs for CAR-T Cell Therapy: Development of an Efficient Sampling Strategy Through Optimal Experimental Design
-
In Silico Clinical Trials in Drug Development: A Systematic Review
Part of Therapeutic Innovation and Regulatory Science, p. 423-439, 2026
- DOI for In Silico Clinical Trials in Drug Development: A Systematic Review
- Download full text (pdf) of In Silico Clinical Trials in Drug Development: A Systematic Review
-
Part of CPT, p. 1857-1868, 2025
- DOI for Integrated Modeling of Digital-Motor and Clinician-Reported Outcomes Using Item Response Theory: Towards Powerful Trials for Rare Neurological Diseases
- Download full text (pdf) of Integrated Modeling of Digital-Motor and Clinician-Reported Outcomes Using Item Response Theory: Towards Powerful Trials for Rare Neurological Diseases
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Part of CPT, p. 1705-1714, 2025
- DOI for A Pharmacometrics-Informed Trial Simulation Framework for Optimizing Study Designs for Disease-Modifying Treatments in Rare Neurological Disorders
- Download full text (pdf) of A Pharmacometrics-Informed Trial Simulation Framework for Optimizing Study Designs for Disease-Modifying Treatments in Rare Neurological Disorders
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Leveraging Model Master Files for Long-Acting Injectables
Part of Pharmaceutical research, p. 747-752, 2025
- DOI for Leveraging Model Master Files for Long-Acting Injectables
- Download full text (pdf) of Leveraging Model Master Files for Long-Acting Injectables
All publications
Articles in journal
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Part of CPT, 2026
- DOI for Optimizing Clinical Study Designs for CAR-T Cell Therapy: Development of an Efficient Sampling Strategy Through Optimal Experimental Design
- Download full text (pdf) of Optimizing Clinical Study Designs for CAR-T Cell Therapy: Development of an Efficient Sampling Strategy Through Optimal Experimental Design
-
Part of CPT, p. 1857-1868, 2025
- DOI for Integrated Modeling of Digital-Motor and Clinician-Reported Outcomes Using Item Response Theory: Towards Powerful Trials for Rare Neurological Diseases
- Download full text (pdf) of Integrated Modeling of Digital-Motor and Clinician-Reported Outcomes Using Item Response Theory: Towards Powerful Trials for Rare Neurological Diseases
-
Part of CPT, p. 1705-1714, 2025
- DOI for A Pharmacometrics-Informed Trial Simulation Framework for Optimizing Study Designs for Disease-Modifying Treatments in Rare Neurological Disorders
- Download full text (pdf) of A Pharmacometrics-Informed Trial Simulation Framework for Optimizing Study Designs for Disease-Modifying Treatments in Rare Neurological Disorders
-
Leveraging Model Master Files for Long-Acting Injectables
Part of Pharmaceutical research, p. 747-752, 2025
- DOI for Leveraging Model Master Files for Long-Acting Injectables
- Download full text (pdf) of Leveraging Model Master Files for Long-Acting Injectables
-
Part of BMC Medical Research Methodology, 2025
- DOI for Comparing randomized trial designs to estimate treatment effect in rare diseases with longitudinal models: a simulation study showcased by Autosomal Recessive Cerebellar Ataxias using the SARA score
- Download full text (pdf) of Comparing randomized trial designs to estimate treatment effect in rare diseases with longitudinal models: a simulation study showcased by Autosomal Recessive Cerebellar Ataxias using the SARA score
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Reflection on clinical and methodological issues in rare disease clinical trials.
Part of Orphanet Journal of Rare Diseases, 2025
- DOI for Reflection on clinical and methodological issues in rare disease clinical trials.
- Download full text (pdf) of Reflection on clinical and methodological issues in rare disease clinical trials.
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Part of Statistics in Medicine, 2025
- DOI for A Comparison of Statistical Methods for Time-To-Event Analyses in Randomized Controlled Trials Under Non-Proportional Hazards
- Download full text (pdf) of A Comparison of Statistical Methods for Time-To-Event Analyses in Randomized Controlled Trials Under Non-Proportional Hazards
-
Part of CPT, p. 270-280, 2024
- DOI for Optimizing the design of a pharmacokinetic trial to evaluate the dosing scheme of a novel tuberculosis drug in children living with or without HIV
- Download full text (pdf) of Optimizing the design of a pharmacokinetic trial to evaluate the dosing scheme of a novel tuberculosis drug in children living with or without HIV
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Part of CPT, p. 1748-1761, 2024
- DOI for Evaluation of model-integrated evidence approaches for pharmacokinetic bioequivalence studies using model averaging methods
- Download full text (pdf) of Evaluation of model-integrated evidence approaches for pharmacokinetic bioequivalence studies using model averaging methods
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A fully automatic tool for development of population pharmacokinetic models
Part of CPT, p. 1784-1797, 2024
- DOI for A fully automatic tool for development of population pharmacokinetic models
- Download full text (pdf) of A fully automatic tool for development of population pharmacokinetic models
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Part of Clinical Pharmacology and Therapeutics, p. 1593-1605, 2024
- DOI for Longitudinal Analysis of Natural History Progression of Rare and Ultra‐Rare Cerebellar Ataxias Using Item Response Theory
- Download full text (pdf) of Longitudinal Analysis of Natural History Progression of Rare and Ultra‐Rare Cerebellar Ataxias Using Item Response Theory
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Part of CPT, p. 1734-1747, 2024
- DOI for Development and comparison of model-integrated evidence approaches for bioequivalence studies with pharmacokinetic end points
- Download full text (pdf) of Development and comparison of model-integrated evidence approaches for bioequivalence studies with pharmacokinetic end points
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Part of CPT, p. 1327-1340, 2024
- DOI for Item performance of the scale for the assessment and rating of ataxia in rare and ultra-rare genetic ataxias
- Download full text (pdf) of Item performance of the scale for the assessment and rating of ataxia in rare and ultra-rare genetic ataxias
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Part of Computational Statistics & Data Analysis, 2024
- DOI for Optimizing designs in clinical trials with an application in treatment of Epidermolysis bullosa simplex, a rare genetic skin disease
- Download full text (pdf) of Optimizing designs in clinical trials with an application in treatment of Epidermolysis bullosa simplex, a rare genetic skin disease
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The Role of Model Master Files for Sharing, Acceptance, and Communication with FDA
Part of AAPS Journal, 2024
-
Generation and application of avatars in pharmacometric modelling
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 411-423, 2023
- DOI for Generation and application of avatars in pharmacometric modelling
- Download full text (pdf) of Generation and application of avatars in pharmacometric modelling
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How to Analyze Continuous and Discrete Repeated Measures in Small-Sample Cross-Over Trials?
Part of Biometrics, p. 3998-4011, 2023
-
Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
Part of Orphanet Journal of Rare Diseases, 2023
- DOI for Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
- Download full text (pdf) of Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
-
Part of AAPS Journal, 2021
- DOI for Bounded Integer Modeling of Symptom Scales Specific to Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia
- Download full text (pdf) of Bounded Integer Modeling of Symptom Scales Specific to Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia
-
Pharmacometrics meets statistics-A synergy for modern drug development
Part of CPT, p. 1134-1149, 2021
- DOI for Pharmacometrics meets statistics-A synergy for modern drug development
- Download full text (pdf) of Pharmacometrics meets statistics-A synergy for modern drug development
-
Tutorial for $DESIGN in NONMEM: Clinical trial evaluation and optimization
Part of CPT, p. 1452-1465, 2021
- DOI for Tutorial for $DESIGN in NONMEM: Clinical trial evaluation and optimization
- Download full text (pdf) of Tutorial for $DESIGN in NONMEM: Clinical trial evaluation and optimization
-
Part of Clinical Pharmacology and Therapeutics, p. 1190-1195, 2021
- DOI for Public Workshop Summary Report on Fiscal Year 2021 Generic Drug Regulatory Science Initiatives: Data Analysis and Model-Based Bioequivalence.
- Download full text (pdf) of Public Workshop Summary Report on Fiscal Year 2021 Generic Drug Regulatory Science Initiatives: Data Analysis and Model-Based Bioequivalence.
-
Part of Clinical Pharmacology in Drug Development, p. 220-228, 2021
-
Part of AAPS Journal, 2020
- DOI for Item Response Theory Modeling of the International Prostate Symptom Score in Patients with Lower Urinary Tract Symptoms Associated with Benign Prostatic Hyperplasia
- Download full text (pdf) of Item Response Theory Modeling of the International Prostate Symptom Score in Patients with Lower Urinary Tract Symptoms Associated with Benign Prostatic Hyperplasia
-
Population Pharmacokinetics and Dosing of Ethionamide in Children with Tuberculosis
Part of Antimicrobial Agents and Chemotherapy, 2020
-
Part of AAPS Journal, 2020
- DOI for Saddle-Reset for Robust Parameter Estimation and Identifiability Analysis of Nonlinear Mixed Effects Models
- Download full text (pdf) of Saddle-Reset for Robust Parameter Estimation and Identifiability Analysis of Nonlinear Mixed Effects Models
-
Optimizing Dose-Finding Studies for Drug Combinations Based on Exposure-Response Models
Part of AAPS Journal, 2019
-
Feasibility of Exposure-Response Analyses for Clinical Dose-Ranging Studies of Drug Combinations
Part of AAPS Journal, 2018
-
Adaptive Optimal Designs for Dose-Finding Studies with Time-to-Event Outcomes
Part of AAPS Journal, 2018
- DOI for Adaptive Optimal Designs for Dose-Finding Studies with Time-to-Event Outcomes
- Download full text (pdf) of Adaptive Optimal Designs for Dose-Finding Studies with Time-to-Event Outcomes
-
A Population Pharmacokinetic-Pharmacodynamic Model of Pegfilgrastim
Part of AAPS Journal, 2018
- DOI for A Population Pharmacokinetic-Pharmacodynamic Model of Pegfilgrastim
- Download full text (pdf) of A Population Pharmacokinetic-Pharmacodynamic Model of Pegfilgrastim
-
Part of AAPS Journal, 2018
- DOI for Implementing Optimal Designs for Dose-Response Studies Through Adaptive Randomization for a Small Population Group
- Download full text (pdf) of Implementing Optimal Designs for Dose-Response Studies Through Adaptive Randomization for a Small Population Group
-
Part of AAPS Journal, 2018
- DOI for Model-Based Adaptive Optimal Design (MBAOD) Improves Combination Dose Finding Designs: an Example in Oncology
- Download full text (pdf) of Model-Based Adaptive Optimal Design (MBAOD) Improves Combination Dose Finding Designs: an Example in Oncology
-
The Standard Output: A Tool-Agnostic Modeling Storage Format
Part of CPT, p. 543-546, 2018
- DOI for The Standard Output: A Tool-Agnostic Modeling Storage Format
- Download full text (pdf) of The Standard Output: A Tool-Agnostic Modeling Storage Format
-
Reduced and optimized trial designs for drugs described by a target mediated drug disposition model
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 637-647, 2018
- DOI for Reduced and optimized trial designs for drugs described by a target mediated drug disposition model
- Download full text (pdf) of Reduced and optimized trial designs for drugs described by a target mediated drug disposition model
-
Model-Informed Drug Development and Review for Generic Products: Summary Of FDA Public Workshop
Part of Clinical Pharmacology and Therapeutics, p. 27-30, 2018
-
Model Description Language (MDL): A Standard for Modeling and Simulation
Part of CPT, p. 647-650, 2017
-
Part of CPT, p. 418-429, 2017
-
Model Evaluation of Continuous Data Pharmacometric Models: Metrics and Graphics
Part of CPT, p. 87-109, 2017
- DOI for Model Evaluation of Continuous Data Pharmacometric Models: Metrics and Graphics
- Download full text (pdf) of Model Evaluation of Continuous Data Pharmacometric Models: Metrics and Graphics
-
Assessing robustness of designs for random effects parameters for nonlinear mixed-effects models
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 611-616, 2017
-
Model selection and averaging of nonlinear mixed-effect models for robust phase III dose selection
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 581-597, 2017
- DOI for Model selection and averaging of nonlinear mixed-effect models for robust phase III dose selection
- Download full text (pdf) of Model selection and averaging of nonlinear mixed-effect models for robust phase III dose selection
-
Part of Pharmaceutical research, p. 1125-1133, 2017
-
The effect of using a robust optimality criterion in model based adaptive optimization.
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 317-324, 2017
- DOI for The effect of using a robust optimality criterion in model based adaptive optimization.
- Download full text (pdf) of The effect of using a robust optimality criterion in model based adaptive optimization.
-
Part of AAPS Journal, p. 505-518, 2016
-
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 609-619, 2016
- DOI for The effect of Fisher information matrix approximation methods in population optimal design calculations
- Download full text (pdf) of The effect of Fisher information matrix approximation methods in population optimal design calculations
-
PopED lite: an optimal design software for preclinical pharmacokinetic and pharmacodynamic studies
Part of Computer Methods and Programs in Biomedicine, p. 126-143, 2016
-
A diagnostic tool for population models using non-compartmental analysis: The ncappc package for R
Part of Computer Methods and Programs in Biomedicine, p. 83-93, 2016
- DOI for A diagnostic tool for population models using non-compartmental analysis: The ncappc package for R
- Download full text (pdf) of A diagnostic tool for population models using non-compartmental analysis: The ncappc package for R
-
Accelerating Monte Carlo power studies through parametric power estimation
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 223-234, 2016
- DOI for Accelerating Monte Carlo power studies through parametric power estimation
- Download full text (pdf) of Accelerating Monte Carlo power studies through parametric power estimation
-
Part of CPT, p. 316-319, 2015
- DOI for Pharmacometrics Markup Language (PharmML): Opening New Perspectives for Model Exchange in Drug Development
- Download full text (pdf) of Pharmacometrics Markup Language (PharmML): Opening New Perspectives for Model Exchange in Drug Development
-
Part of British Journal of Clinical Pharmacology, p. 116-127, 2015
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Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 211-224, 2015
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Part of British Journal of Clinical Pharmacology, p. 6-17, 2015
-
Part of Journal of Nutrition, p. 1674-1680, 2014
-
Optimal clinical trial design based on a dichotomous Markov-chain mixed-effect sleep model
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 639-654, 2014
- DOI for Optimal clinical trial design based on a dichotomous Markov-chain mixed-effect sleep model
- Download full text (pdf) of Optimal clinical trial design based on a dichotomous Markov-chain mixed-effect sleep model
-
Part of Pharmaceutical research, p. 2152-2165, 2014
- DOI for Improved Utilization of ADAS-cog Assessment Data through Item Response Theory based Pharmacometric Modeling
- Download full text (pdf) of Improved Utilization of ADAS-cog Assessment Data through Item Response Theory based Pharmacometric Modeling
-
Evaluation of Bias, Precision, Robustness and Runtime for Estimation Methods in NONMEM 7
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 223-238, 2014
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Part of CPT, 2013
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Modeling and Simulation Workbench for NONMEM: Tutorial on Pirana, PsN, and Xpose
Part of CPT, 2013
-
Optimizing disease progression study designs for drug effect discrimination
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 587-596, 2013
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Part of NeuroImage, p. 160-169, 2013
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Simultaneous optimal experimental design for in vitro binding parameter estimation
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 573-585, 2013
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Chain length of dietary alkylresorcinols affects their in vivo elimination kinetics in rats
Part of Journal of Nutrition, p. 1573-1578, 2013
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PopED: An extended, parallelized, nonlinear mixed effects models optimal design tool
Part of Computer Methods and Programs in Biomedicine, p. 789-805, 2012
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Ethically Attractive Dose-Finding Designs for Drugs With a Narrow Therapeutic Index
Part of Journal of clinical pharmacology, p. 29-38, 2012
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Part of Journal of clinical pharmacology, p. 347-360, 2012
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Serial correlation in optimal design for nonlinear mixed effects models
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 239-249, 2012
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Plasma and Cerebrospinal Fluid Pharmacokinetics of Naproxen in Children
Part of Journal of clinical pharmacology, p. 1516-1526, 2012
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Part of NeuroImage, p. 849-856, 2012
-
Part of Clinical Pharmacology and Therapeutics, p. 863-871, 2012
-
Prediction-Corrected Visual Predictive Checks for Diagnosing Nonlinear Mixed-Effects Models
Part of AAPS Journal, p. 143-151, 2011
-
Optimal Design in Population Kinetic Experiments by Set-Valued Methods
Part of AAPS Journal, p. 495-507, 2011
-
Part of AAPS Journal, p. 445-463, 2011
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A Fast Method for Testing Covariates in Population PK/PD Models
Part of AAPS Journal, p. 464-472, 2011
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Part of Drug Metabolism And Disposition, p. 858-863, 2011
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Adaptive-Optimal Design in PET Occupancy Studies
Part of Clinical Pharmacology and Therapeutics, p. 563-571, 2010
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Plasma and cerebrospinal fluid pharmacokinetics of flurbiprofen in children
Part of British Journal of Clinical Pharmacology, p. 557-566, 2010
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Part of Pharmaceutical research, p. 866-877, 2010
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Part of AAPS Journal, p. 148-154, 2009
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Trial treatment length optimization with an emphasis on disease progression studies
Part of Journal of clinical pharmacology, p. 323-335, 2009
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Simultaneous optimal experimental design on dose and sample times
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 125-145, 2009
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Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 281-295, 2009
- DOI for Optimization of the intravenous glucose tolerance test in T2DM patients using optimal experimental design
- Download full text (pdf) of Optimization of the intravenous glucose tolerance test in T2DM patients using optimal experimental design
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Part of Clinical Pharmacology and Therapeutics, p. 111-118, 2008
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Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 117-137, 2008
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Pharmacokinetics of P-glycoprotein inhibition in the rat blood-brain barrier
Part of Journal of Pharmaceutical Sciences, p. 5386-5400, 2008
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Conditional weighted residuals (CWRES): a model diagnostic for the FOCE method
Part of Pharmaceutical research, p. 2187-2197, 2007
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Automated identification of axonal growth cones in time-lapse image sequences.
Part of Journal of Neuroscience Methods, p. 232-8, 2006
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Simultaneous population optimal design for pharmacokinetic-pharmacodynamic experiments.
Part of AAPS Journal, 2005
-
Robust population pharmacokinetic experiment design.
Part of Journal of Pharmacokinetics and Pharmacodynamics, p. 33-64, 2005
-
POPED, a software for optimal experiment design in population kinetics.
Part of Computer Methods and Programs in Biomedicine, p. 29-46, 2004
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An evaluation of population D-optimal designs via pharmacokinetic simulations.
Part of Annals of Biomedical Engineering, p. 98-111, 2003
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Part of Circulation, p. 851-6, 2003
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Classical examination of the Stark effect in hydrogen
Part of Physical Review A. Atomic, Molecular, and Optical Physics, p. 4609-4612, 1997
Articles, review/survey
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In Silico Clinical Trials in Drug Development: A Systematic Review
Part of Therapeutic Innovation and Regulatory Science, p. 423-439, 2026
- DOI for In Silico Clinical Trials in Drug Development: A Systematic Review
- Download full text (pdf) of In Silico Clinical Trials in Drug Development: A Systematic Review
-
Methods for non-proportional hazards in clinical trials: A systematic review
Part of Statistical Methods in Medical Research, p. 1069-1092, 2024
- DOI for Methods for non-proportional hazards in clinical trials: A systematic review
- Download full text (pdf) of Methods for non-proportional hazards in clinical trials: A systematic review
-
Part of CPT, p. 624-630, 2023
- DOI for Establishing the suitability of model-integrated evidence to demonstrate bioequivalence for long-acting injectable and implantable drug products: Summary of workshop
- Download full text (pdf) of Establishing the suitability of model-integrated evidence to demonstrate bioequivalence for long-acting injectable and implantable drug products: Summary of workshop
-
Metaheuristics for pharmacometrics
Part of CPT, p. 1297-1309, 2021
- DOI for Metaheuristics for pharmacometrics
- Download full text (pdf) of Metaheuristics for pharmacometrics
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Population pharmacometrics in support of analgesics studies
Part of Acta Anaesthesiologica Scandinavica, p. 143-156, 2014