Conference Agenda
Overview and details of the sessions of this conference. Please select a date or location to show only sessions at that day or location. Please select a single session for detailed view (with abstracts and downloads if available).
|
Session Overview | |
Location: Biozentrum U1.141 Biozentrum, 124 seats |
Date: Sunday, 24/Aug/2025 | |
9:00am - 10:30am |
Network meta-analysis: from key concepts to advanced methods Virginia Chiocchia1, Konstantina Chalkou1, Orestis Efthimiou2, Tasnim Hamza1, Georgia Salanti1 1: Institute of Social and Preventive Medicine, University of Bern, Switzerland; 2: Institute of Primary Health Care (BIHAM), University of Bern, Switzerland Location: Biozentrum U1.141 |
11:00am - 12:30pm |
Network meta-analysis: from key concepts to advanced methods Location: Biozentrum U1.141 |
1:30pm - 3:00pm |
Network meta-analysis: from key concepts to advanced methods Location: Biozentrum U1.141 |
3:30pm - 5:00pm |
Network meta-analysis: from key concepts to advanced methods Location: Biozentrum U1.141 |
Date: Monday, 25/Aug/2025 | |
11:30am - 1:00pm |
Poster Highlights Location: Biozentrum U1.141 |
2:00pm - 3:30pm |
Adaptive and multi-arm multi-stage trials Location: Biozentrum U1.141 Confidence intervals in two-stage adaptive enrichment designs Dynamic Bayesian Sample Size Re-Estimation: Balancing Historical and Real-Time Data in Adaptive Clinical Trials MAMS with patient reported outcomes and treatments with different modalities: how should we handle a differential placebo effect? Multi-arm multi-stage (MAMS) randomised selection designs: With an application to miscarriage and surgical platform trials A test for treatment differences using allocation probabilities in response-adaptive clinical trials |
4:00pm - 5:30pm |
Clinical trials and regulatory issues Location: Biozentrum U1.141 Compatible Effect Estimation and Hypothesis Testing in Drug Regulation Opportunities to speed up IVD adoption and patient access in the UK: the pre-eclampsia testing timeline Statistical review of regulatory requirements for AI diagnosis Validating Physiologically-based Pharmacokinetic Models using the Continuous Ranked Probability Score: Beyond Being Correct on Average Conditional Marketing Authorisation based on the Intermediate Endpoint of a Randomised Clinical Trial: Dual or Co-Primary Endpoints? |
Date: Tuesday, 26/Aug/2025 | |
9:15am - 10:45am |
Bayesian methods 2 Location: Biozentrum U1.141 Using a foundation model for detecting and reducing site-specific differences in federated meta-analysis of regression models Sample size calculations for prediction model development: A general Bayesian-framework using posterior distributions to examine expected performance, degradation and stability Efficient Utilization of Dose-Schedule Grids for Optimal Therapeutic Outcomes in Non-Oncology Settings On the interplay between prior weight and vague variance in Robust Mixture Priors Bayesian nonparametric methods for inferring causal effects of longitudinal treatments amidst missing covariate data |
11:30am - 1:00pm |
Alternative estimands in causal inference Location: Biozentrum U1.141 Assumption-lean modeling for patient-centered decision-making Causal inference targeting a concentration index for studies of health inequalities Rethinking the Win Ratio: A Causal Framework for Hierarchical Outcome Analysis Assessing individual-level uncertainty of causal predictions through the causal effective sample size Estimating Win Ratio for Prioritized Composite Outcomes in the Presence of Noncompliance |
Date: Wednesday, 27/Aug/2025 | |
9:00am - 10:30am |
Competing events and multi-state modelling Location: Biozentrum U1.141 A general approach to fitting multistate cure models based on an extended-long-format data structure Calibration of cause-specific absolute risk for external validation using each cause-specific hazards model in the presence of competing events Multi-state models with restricted transition windows: The impact of time scale choice Integrating Landmarking and Competing Risks in Survival Analysis with Machine Learning Techniques Survival without vs after transition to the intermediate event in a non-markovian “illness-death” model: application to heart transplant data |
2:00pm - 3:30pm |
Survival analysis 2 Location: Biozentrum U1.141 A framework for estimating, investigating and using the correlation between multiple time-to-event endpoints in a group sequential trial Likelihood adaptively incorporated external aggregate information with uncertainty for survival data A new statistical test to compare probability of being in response (PBR) with application to a study in oncology One-sample survival tests for non-proportional hazards in oncology clinical trials Efficiency of Nonparametric Superiority Tests Based on Restricted Mean Survival Time Versus the Logrank Test Under Proportional Hazards |
4:00pm - 5:30pm |
Survival analysis 3 Location: Biozentrum U1.141 Estimating the new event-free survival Marginal Matched Pairs Cox Regression Using Restricted Mean Survival Time under proportional hazards in a non-inferiority randomised trial with time-to-event outcome Variable selection methodology for illness-death model with interval censored data Modelling the time-varying effect of hormonal treatment on metastasis-free survival among ER+ breast cancer patients - a natural history modelling approach |
Contact and Legal Notice · Contact Address: Privacy Statement · Conference: ISCB46 |
Conference Software: ConfTool Pro 2.6.154+TC © 2001–2025 by Dr. H. Weinreich, Hamburg, Germany |