2024 Rome, Italy

III-01 Oliver Ackaert
Building a reproducible pharmacometrics environment to ensure quality, continuity, efficiency, and good communication
Thursday 10:15-11:45
III-02 Linda Aulin
Tapping into the potential of pharmacometrics in preclinical infection models: a low-hanging fruit or joined efforts needed?
Thursday 10:15-11:45
III-03 Emily Behrens
Influence of interoccasion variability on parameter estimates of a population pharmacokinetic model under various sparse study designs
Thursday 10:15-11:45
III-04 Brigitta Bodak
Facilitating structural population PK model building for pharmacometricians and beyond
Thursday 10:15-11:45
III-05 Fan Cheng
Favipiravir pharmacokinetics in immunocompromised infants and children with chronic RNA viral infections
Thursday 10:15-11:45
III-06 S. Y. Amy Cheung
Predicting RSV prophylaxis in the infant target population – assessing monoclonal antibody versus maternal vaccination efficacy using MBMA
Thursday 10:15-11:45
III-07 Marc Codaccioni
Predictive performance of two hepatic CYP3A4 ontogeny within a paediatric PBPK model.
Thursday 10:15-11:45
III-08 Alessandro Di Deo
A model-based algorithm for mycophenolate dose adjustment in paediatric transplantation patients
Thursday 10:15-11:45
III-09 Lucia Diaz Garcia
Individualized tacrolimus dosing in pediatric kidney transplantation: development of PBPK-based predictive models, simulations and applications (ModSimTer-Tacro Study)
Thursday 10:15-11:45
III-10 Summer Feng
Exposure-safety Markov modeling of ocular adverse events in patient populations treated with tisotumab vedotin
Thursday 10:15-11:45
III-11 Klervi GOLHEN
Characterizing effect of methotrexate on adalimumab PK in pediatric patients with inflammatory rheumatic disease
Thursday 10:15-11:45
III-12 Silvia Grandoni
Efficacy extrapolation and dose rationale for duloxetine in paediatric chronic pain
Thursday 10:15-11:45
III-13 Yuchen Guo
Generation of realistic virtual adult populations using the NHANES database: a copula approach
Thursday 10:15-11:45
III-14 Niklas Hartung
An information-theoretic evaluation of vine copula models for high-dimensional covariate distributions
Thursday 10:15-11:45
III-15 Matthieu Jacobs
Accounting for uncertainty in the application of generic PBPK workflow to candidate selection
Thursday 10:15-11:45
III-16 Christos Kaikousidis
In Silico Dosimetry Study of Tc99m-Tetrofosmin in Children Using a Novel PBPK Model in Humans Built from SPECT Imaging Data
Thursday 10:15-11:45
III-17 Daniel Kaschek
How to reduce the total number of samples in a bioequivalence study without impacting statistical power
Thursday 10:15-11:45
III-18 Csaba Katai
An asymptotic description of a basic FcRn-regulated clearance mechanism and its implications for PBPK modelling of large antibodies
Thursday 10:15-11:45
III-19 Takayuki Katsube
Global Sensitivity Analysis for Effects of Correlated Covariates Using Shapley Value
Thursday 10:15-11:45
III-20 Lina Keutzer
Model-based experimental design recommendations for in vivo studies of the novel anti-tuberculosis drug MPL-447 improve characterization of PK and PD
Thursday 10:15-11:45
III-21 Feras Khalil
A joint parent-metabolite model to characterize the pharmacokinetic profile of tapentadol and its metabolites in the pediatric population and inform a model-based evaluation of a post-approval commitment pediatric trial
Thursday 10:15-11:45
III-22 Christina Kovar
Physiologically Based Pharmacokinetic Modeling of Dasatinib to Describe Enzyme-Mediated and pH-Dependent Drug–Drug Interaction Scenarios
Thursday 10:15-11:45
III-23 Mads Kreilgaard
Model-informed development of Mim8 - a novel bispecific antibody for the treatment of haemophilia A
Thursday 10:15-11:45
III-24 Katharina Krollik
Oral absorption modeling of weakly basic drugs – Combining in vitro and in silico models
Thursday 10:15-11:45
III-25 Marie Lambert
Population pharmacokinetic model to assess bone marrow absorbed dose after 177Lu-Dotatate administration
Thursday 10:15-11:45
III-26 Paul Lang
Leveraging Open Systems Biology Standards for Improved Reusability and Reproducibility of Pharmacological Models
Thursday 10:15-11:45
III-27 Julia Larsson
PK and PBPK modeling approaches to describe the lung and systemic exposure after inhalation of AZD4604
Thursday 10:15-11:45
III-28 Félicien Le Louedec
Model-informed precision dosing of high-dose IV busulfan in Thai pediatric patients
Thursday 10:15-11:45
III-29 Félicien Le Louedec
Model-informed precision dosing of protein kinase inhibitors: benefits and limits. The example of imatinib.
Thursday 10:15-11:45
III-30 Maxime Le Merdy
Ocular Exposure Extrapolation Across Multiple Species Using PBPK Modeling and Simulation: Latanoprost Solution Case Study
Thursday 10:15-11:45
III-31 Donghwan Lee
A comparative population pharmacokinetic analysis of nafamostat mesilate in patients receiving extracorporeal membrane oxygenation therapy (ECMO) support: central venous samples vs. ECMO circuit samples
Thursday 10:15-11:45
III-32 Apolline Lefevre
A mechanistic PK/PD model to predict cytokine release and tumor cell killing associated to T-cell bispecific therapies
Thursday 10:15-11:45
III-33 Romain Leroux
Design evaluation and optimisation in nonlinear mixed effects models with the R package PFIM 6.0
Thursday 10:15-11:45
III-34 Xia Li
Model Informed Dose Evaluation for Aticaprant in Adolescent Patients Following the Adult Dose Regimen
Thursday 10:15-11:45
III-35 Andreas Lindauer
e-Campsis: a Shiny PK/PD model simulator based on Campsis
Thursday 10:15-11:45
III-36 Cong Liu
Application of translational physiologically based pharmacokinetic (PBPK) model for elucidating the complex disposition of ADCs: a case study with T-DM1
Thursday 10:15-11:45
III-37 Feiyan Liu
Unravelling the effects of acute inflammation on pharmacokinetics: a model-based analysis focusing on renal excretion and CYP3A4-mediated metabolism
Thursday 10:15-11:45
III-38 Han Liu
Informing the selection of clinically relevant pharmacokinetic target range for Therapeutic Drug Monitoring (TDM) of sunitinib: a pharmacometric simulation framework
Thursday 10:15-11:45
III-39 Sarah Lobet
Influence of body composition on the pharmacokinetics of monoclonal antibodies : example of cetuximab and bevacizumab
Thursday 10:15-11:45
III-40 Helena Loer
Physiologically Based Pharmacokinetic Modeling of Imatinib and Its Main Metabolite for Drug–Drug Interaction Predictions
Thursday 10:15-11:45
III-41 Aurelie Lombard
Exploring the use of constant and time-varying observation-based versus model-based tumour size metrics for early predictions of drug efficacy on overall survival in malignant pleural mesothelioma
Thursday 10:15-11:45
III-42 Orphélie Lootens
Building a physiologically-based pharmacokinetic model for a carcinogenic food contaminant aflatoxin B1
Thursday 10:15-11:45
III-43 Vincent Madelain
Impact of interaction model choice in PKPD analysis evaluating drug combination in TGI in vivo studies
Thursday 10:15-11:45
III-44 Claude Magnard
Pharmacokinetic Modeling of Fentanyl Citrate and Norfentanyl in Calves Using a Nonlinear Mixed-Effects Approach
Thursday 10:15-11:45
III-45 John Maringwa
Partial residual plots (PRPs) as an integrated model diagnostic tool in model-based meta-analysis (MBMA)
Thursday 10:15-11:45
III-46 Srinivas Martha
A meta-analysis of prevalence and incidence of diabetic peripheral neuropathy in Asia
Thursday 10:15-11:45
III-47 Frederico Martins
Establishment of Virtual Bioequivalence via DoE-PBPM Model: A Donepezil Case Study
Thursday 10:15-11:45
III-48 Luca Marzano
Explainable machine learning for time-to-event analysis: exploring time-dependent covariate effects on models of small cell lung cancer
Thursday 10:15-11:45
III-49 Emir Mesic
Population pharmacokinetics of Jesduvroq (daprodustat) in chronic kidney disease patients with anemia
Thursday 10:15-11:45
III-50 Frano Mihaljevic
Automatized reporting in the applications of MonolixSuite
Thursday 10:15-11:45
III-51 Samer Mouksassi
The African applied pharmacometrics training fellowship: 1 year later
Thursday 10:15-11:45
III-52 Mourad Mseddi
Population pharmacokinetics of abiraterone in patients with metastatic castration resistant prostate cancer
Thursday 10:15-11:45
III-53 Ida Neldemo
Application of tumor size modelling and simulations to support the dose selection of BI 907828 for a Phase II study
Thursday 10:15-11:45
III-54 Thi Lien Ngo
Development of a Physiological-Based Pharmacokinetic Model for Ritonavir: Unraveling its Triphasic Effects as CYP3A Inhibitor, CYP3A Inducer, and Pgp Inhibitor.
Thursday 10:15-11:45
III-55 Ana Novakovic
Empirical Power Evaluations of an Item Response Model in Parkinson’s Disease Patients
Thursday 10:15-11:45
III-56 Frances Okibedi
Investigating Alternative Daily Dose Regimens for Bedaquiline in Treatment of Multidrug-Resistant Tuberculosis using an Interactive Shiny Application
Thursday 10:15-11:45
III-57 Jessica Ou
Development of a physiologically-based pharmacokinetic model to understand and predict the disposition of gallium-68 radiolabeled-dendrimers in vivo
Thursday 10:15-11:45
III-58 Theodoros Papathanasiou
Population pharmacokinetics of belantamab mafodotin in relapsed or refractory multiple myeloma patients with severe renal impairment
Thursday 10:15-11:45
III-59 Sara Peribanez
A physiologically-based pharmacokinetic model for V937, a novel oncolytic virus, in mice
Thursday 10:15-11:45
III-60 Antoine Pitoy
Contribution of modelling jointly progression-free survival and biomarker longitudinal data for therapeutic evaluation in oncology
Thursday 10:15-11:45
III-61 Luna Prieto Garcia
An Integrated PBPK-Quantitative Systems Pharmacology Model for Statins to Assess the Variability and Implications of Transporter-Mediated Distribution
Thursday 10:15-11:45
III-62 Alicja Puszkiel
Nivolumab de-escalation in patients with complete response: model-based simulations of alternative dosing regimens and noninferiority clinical trials
Thursday 10:15-11:45
III-63 Federico Reali
A minimal PBPK mice model to support the preclinical development of drugs against tuberculosis.
Thursday 10:15-11:45
III-64 Javier Reig-López
Chirality matters: physiologically based pharmacokinetic modelling of ibuprofen enantiomers
Thursday 10:15-11:45
III-65 Pascale Rietveld
Population pharmacokinetics of intraperitoneal irinotecan and SN-38 in patients with peritoneal metastases from colorectal origin
Thursday 10:15-11:45
III-66 Maša Roganović
Modelling fatigue events in prostate cancer patients on radiotherapy
Thursday 10:15-11:45
III-67 Davide Ronchi
Model-based analysis of patient-derived organoids for evaluating anticancer drugs
Thursday 10:15-11:45
III-68 Alberto Russu
Population pharmacokinetic modeling and bioequivalence clinical trial simulations of niraparib plus abiraterone acetate administered as single-agent combination and dual-acting tablets plus prednisone for the treatment of metastatic castration-resistant prostate cancer
Thursday 10:15-11:45
III-69 Anuraag Saini
Development of mPBPK model to support translation decision-making for novel bispecific therapeutics
Thursday 10:15-11:45
III-70 Ayatallah Saleh
Unravelling the complex inhibition network of voriconazole and its metabolites using a middle-out PBPK approach
Thursday 10:15-11:45
III-71 Javier Sanchez Fernandez
Building evidence on the PKPD relationship with bispecific co-stimulatory antibodies using in vitro data: FAP-4-1BBL example
Thursday 10:15-11:45
III-72 Aymara Sancho
Mechanistic characterization of oscillatory patterns in unperturbed tumor growth dynamics: the interplay between cancer cells and components of the tumor microenvironment.
Thursday 10:15-11:45
III-73 Keshava Sannala
Comparison of Pumas and NONMEM in parameter estimation of a complex pharmacodynamic model
Thursday 10:15-11:45
III-74 Darlene Santiago
A Pharmacometric approach for opioid use disorder in Puerto Rico: A research agenda to individualize buprenorphine pharmacotherapy.
Thursday 10:15-11:45
III-75 Emilie Schindler
Population PK-PD modeling and exposure-response analysis in multiple myeloma patients treated with intravenous forimtamig, a T-cell engaging 2:1 bispecific antibody targeting GPRC5D and CD3
Thursday 10:15-11:45
III-76 Miriam Schirru
A QSP model for predicting efficacy assessment of combined treatment of radiotherapy and anti-PD-1 for NSCLC patients through virtual clinical trials.
Thursday 10:15-11:45
III-77 Alejandro Serrano Alcaide
Application of an immune-oncology framework to explore the role of regulatory T cells in antitumor response.
Thursday 10:15-11:45
III-78 Raman Sharma
A meta-analysis for predicting early bactericidal activity of beta-lactam antibiotics against pulmonary tuberculosis
Thursday 10:15-11:45
III-79 Hinke Siebinga
Optimizing radionuclide therapy with 177Lu-HA-DOTATATE in patients with neuroendocrine tumors using semi-physiological population PK models
Thursday 10:15-11:45
III-80 Hanna Silber Baumann
Dose confirmation based on population pharmacokinetics within LUMINESCE (NCT04963270); a Phase III, randomized, double-blind, placebo-controlled study evaluating satralizumab in patients with generalized myasthenia gravis
Thursday 10:15-11:45
III-81 Erik Sjögren
Mechanistic modelling of bioavailability and local immunogenicity after subcutaneous administration within the Open Systems Pharmacology framework
Thursday 10:15-11:45
III-82 Tomás Sou
Population PK/PD modelling of platelet dynamics for dose selection in patients with haematological malignancies
Thursday 10:15-11:45
III-83 Viktoria Stachanow
Drug and target parameters impacting target profiles for mono- and multi-specific NANOBODY® molecules – a model-based sensitivity analysis
Thursday 10:15-11:45
III-84 Herbert Struemper
Development of a joint tumor size (TS)–overall survival (OS) modelling and simulation (M&S) framework supporting oncology development decision making
Thursday 10:15-11:45
III-85 Huybrecht T'jollyn
Individual virtual controls as surrogate for a control arm – application for siRNA and NA therapy in chronic hepatitis B infection
Thursday 10:15-11:45
III-86 Zhiyuan Tan
Population pharmacokinetic analysis of pazopanib in adult patients with metastatic renal cell carcinoma and soft tissue sarcoma
Thursday 10:15-11:45
III-87 David Ternant
A multi drug disposition model accounting for rituximab antigen binding portion (Fab) and crystallizable (Fc) mediated drug disposition mechanisms
Thursday 10:15-11:45
III-88 Paul Thoueille
Pharmacometrics-based analysis of long-acting cabotegravir over 6 months in real-life people living with HIV in Switzerland
Thursday 10:15-11:45
III-89 Pauline Traynard
Bayesian individual dynamic predictions via a convenient R function using MonolixSuite
Thursday 10:15-11:45
III-90 Cristian Valiante
PBPK model-based extrapolation from adults to children to predict furosemide oral solution bioavailability
Thursday 10:15-11:45
III-91 Anne van Rongen
Quantification of renal drug clearance in neonates born Small for Gestational Age (SGA) compared to neonates born Appropriate for Gestational Age (AGA)
Thursday 10:15-11:45
III-92 Sergei Vavilov
R framework for reproducible and quality-controlled modeling and simulation with the Open Systems Pharmacology Software
Thursday 10:15-11:45
III-93 Yunjiao Wu
When will the glomerular filtration rate in preterm neonates catch up to their term peers?
Thursday 10:15-11:45
III-94 Tan Zhang
Exploring the impact of obesity on drug clearance using PBPK modelling approaches: influential variables affecting scaling from non-obese to obese subjects for drugs metabolized in the liver
Thursday 10:15-11:45
III-95 Han Zheng
MaS: population pharmacometric modeling in Python
Thursday 10:15-11:45
III-96 Yuanxi Zou
Evaluating two strategies for the design of pediatric pharmacokinetic studies
Thursday 10:15-11:45