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21-23 October 2026
Leiden - The Netherlands
Scientific Committee
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Scientific Committee
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Bayes 2025
DAY 1 – 22 October 2025
TIME
SPEAKER
AFFILIATION
08:30 - 09:00
Registration
09:00 - 12:30
Marco Scutari
Dalle Molle Institute for Artificial Intelligence and Consultant, Lugano, CH
Short course "Bayesian and Causal Networks for Clinical and Epidemiological Data: Concepts, Implementation and Interpretation"
npj Digital Medicine
notebooks
Aime
12:30 - 13:30
Lunch
13:30 - 13:40
Welcome and opening
Arnaud Monseur
Cencora-Pharmalex, Belgium on behalf of The Adolphe Quetelet Society
Brad Carlin
Scientific Committee
Chair person: SOFIA VILLAR
13:40 - 14:10
Virgilio Gómez Rubio
University of Castilla-La Mancha, Spain
Approximate Bayesian inference for the analysis of population health data
14:10 - 14:30
Suyu Liu
The UT MD Anderson Cancer Center, USA
A Phase I Dose-Finding Design Incorporating Intra-Patient Dose Escalation
14:30 - 14:50
Pantelis Vlachos
Cytel Inc., Switzerland
Evaluating Bayesian and Frequentist Analysis Options for an Oncology Study Design with Non-Proportional Hazards Assumptions
14:50 - 15:10
Brad Carlin
PhaseV Trials, Inc., USA
Optimal Bayesian Adaptive Sequential Trial Design using Stepwise Monte Carlo for Increased Flexibility and Robustness
15:10 - 15:30
Danila Azzolina
Biostatistics and Clinical Trial Methodology Unit, Clinical Research Center, DEMeTra, Department of Translational Medicine, University of Naples Federico II, Italy
SMART-Vent: A Bayesian Adaptive Platform Trial for Evaluating Mechanical Ventilation Strategies Using Patient-Centered Endpoints in Heterogeneous ICU Populations
Chair person: BRUNO BOULANGER
15:30 - 15:45
MY TALK IN 5 MINUTES
Josefina Correa
MIT - Massachusetts Institute of Technology, USA
Bayesian Hierarchical Autoregressive Parametric Estimation with Application to the Analysis of Multilevel Electroencephalogram Signals
Luwis Diya
Johnson & Johnson Innovative Medicine, Beerse, Belgium
Utilizing Informative Priors in Group Comparisons with Completely Censored Data
Helene H Thygesen
Odense University Hospital, Denmark
Play-the-winner trials: Bayesian effect size estimators and design considerations
15:45 - 16:10
Coffee break
Chair person: ASTRID JULLION
16:10 - 16:40
Harrison Quick
University of Minnesota, USA
The Intersection of Informative Priors and Differential Privacy in Bayesian Spatial Biostatistics
16:40 - 17:00
Emmanuel Lesaffre
KULeuven
The functional uniform prior
An exploration towards its usefulness in non-linear (mixed) models
17:00 - 17:20
Zhi Cao
University of Cambridge, Cambridge, UK
Bayesian bivariate analysis of phase II basket trials enabling borrowing of information
DAY 2 – 23 October 2025
TIME
SPEAKER
AFFILIATION
Chair person: PETER VAN DE VEN
08:45 - 09:15
Juan José Abellan
EMA, NL
Towards (long overdue) regulatory guidance on Bayesian statistics in clinical trials
09:15 - 09:35
J. Kyle Wathen
Cytel Inc., USA
Interim Decision Rules for Early “Go” or Futility: A Comparative Assessment of Bayesian and Frequentist Approaches
09:35 - 09:55
Ruitao Lin
The University of Texas MD Anderson Cancer Center, USA
Bayesian design and analysis methods for decentralized clinical trials
09:55 - 10:15
Lorna Wheaton
University of Leicester,UK
A Bayesian model for surrogate endpoint evaluation in mixed biomarker patient populations
10:15 - 10:40
Coffee break
10:40 - 11:10
Andy Grieve
King’s College London, London, UK
Predictive and Pre-Posterior Distributions in the Planning of Clinical Trials
11:10 - 11:40
Nicky Best
GSK London, UK
Beyond the Classical Type I Error: Bayesian Metrics for Bayesian Designs Using Informative Priors
11:40 - 12:15
Panelists:
Nicky Best, Andy Grieve, Sofia Villar, Juan Josè Abellan
Moderator:
Brad Carlin
Panel session Bayes in Regulatory Science
12:15 - 13:15
Lunch
Chair person: GIANLUCA BAIO
13:15 - 13:45
Nicky Welton
University of Bristol, UK
Multi-level Network Meta-Regression (ML-NMR) for population adjustment in Health Technology Assessment
13:45 - 14:05
Emma K. Mackay
Institute of Health Policy, Management and Evaluation, University of Toronto
The Challenge of Precision Medicine in Oncology: Bayesian Solutions for a Changing Landscape in Health Technology Assessment
14:05 - 14:25
Andrea Gabrio
Department of Methodology and Statistics at Maastricht University, NL
A Bayesian modelling framework for health care resource use and costs in trial-based economic evaluations
14:25 - 14:45
Martin Bøg
Novo Nordisk A/S, Søborg, Denmark
A Unified Approach to integrating Dose-Response and Time-Course Estimation in Bayesian network meta-analysis
14:45 - 15:05
Fabio Rigat
AstraZeneca, UK
Design and analysis of clinical trials using Bayesian non-parametrics – application to single arm dose escalation studies
15:05 - 15:30
Coffee break
15:30 - 15:50
Juho Timonen
Generable Inc., USA
Personalized dosing decision using multistate modeling
15:50 - 16:10
Jean-François Michiels
Cencora-Pharmalex, Belgium
Robust Bayesian model for the determination of the confirmatory cut point during the immunogenicity assessment
Chair person: BRUNO BOULANGER
16:10 - 16:30
Laurent Natalis
Cencora-Pharmalex, Belgium
Insight on vaccine stability based on accelerated stability data, Advanced Kinetic Modelling, and Bayesian statistics
16:30 - 16:50
Lian Mae T. Tabien
UP School of Statistics, The Philippines
Bayesian Decision Limits for Correlated Analytes: A Multivariate Regression Approach with Non-Informative and Conjugate Priors
DAY 3 – 24 October 2025
TIME
SPEAKER
AFFILIATION
Chair person: Juan José Abellan
08:30 - 08:50
Georgios Nikolaidis
IQVIA, UK
Incorporating comparative Real-World Evidence in trial-level surrogate endpoint evaluation using adaptive information-sharing methods: a case study in Acute Myeloid Leukemia
08:50 - 09:10
Martin Oliver Sailer
Boehringer Ingelheim Pharma GmbH & Co. KG, Germany
Bayesian borrowing for pediatric extrapolation is easy. Not.
09:10 - 09:30
Dina Jankovic
Centre for Health Economics, University of York, USA
Methods for the elicitation of Bayesian informative priors on stage-sojourn time to inform multi-cancer natural history modelling
09:30 - 09:50
Arlene Jiang
Hospital for Sick Children in Toronto, Ontario, Canada
Optimizing Power in Bayesian Survival Modelling for Rare Diseases
Chair person: BRUNO BOULANGER
09:50 - 10:05
MY TALK IN 5 MINUTES
Giles Partington
Phastar, UK
Bayesian Methods in Registered Clinical Trials: A Systematic Review of Studies Registered on ClinicalTrials.gov
Trevor Wrobleski
London School of Economics, UK
Efficient Bayesian Experimental Design for Benchmark Dose Estimation: Effects of Dose Group Allocation with Overdispersed Toxicological Data
Stef Baas
MRC Biostatistics Unit, University of Cambridge, UK
A burn-in(g) question: How long should an initial equal randomization stage be before Bayesian response-adaptive randomization?
10:05 - 10:30
Coffee break
10:30 - 11:00
Lucinda Billingham
University of Birmingham, UK
Using Bayesian trial designs to change clinical practice in rare diseases
11:00 - 11:30
Aysun Cetinyurek Yavuz
Radboud University Medical Centre, NL
Quantifying Uncertainty in the Face of Rarity: Bayesian Methods in Regulatory Contexts
11:30 - 12:05
Panelists:
Lucinda Billingham, Aysun Cetinyurek Yavuz, Peter van de Ven
Moderator:
Arnaud Monseur
Panel session Bayes in Rare Disease
12:05 - 12:55
Working light lunch in the conference room
Instats Junior Researchers Prize
Book raffle sponsored by Chapman & Hall/CRC and Springer
Brad Carlin
PhaseV Trials, Inc., USA
Gianluca Baio
University College London, UK
Closing remarks
Arnaud Monseur
Cencora-Pharmalex, Belgium on behalf of The Adolphe Quetelet Society
Brad Carlin
Scientific Committee