Projects

Select a project to learn more:

• 1. Dose finding for combination trials with many treatments
• 2. Pooling information on progression-free and overall survival in multi-arm cancer trials
• 3. Using pre-clinical information to establish a safe dose in first-in-men studies
• 4. Development of a biomarker score to identify a subgroup of treatment responders
• 5. The impact of data and safety monitoring board decisions to drop treatments
• 6. Optimal designs and analysis methods for the development of Biosimilars
• 7. Subgroup Analyses in Early Phase Clinical Trials
• 8. Innovative designs for combination of existing therapies
• 9. Modelling and simulation for the early development of a modified administration route
• 10. Bias and precision in early phase adaptive studies and its consequences for the decisions about conducting and designing confirmatory studies
• 11. Interval estimation for dose-finding studies
• 12. Statistical methods for phase I/II trials of molecularly targeted agents in oncology
• 13. Statistical aspects of animal to human translation
• 14. Detecting pharmacodynamic drug-drug interactions