19 results on '"Uno, H."'
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2. Beyond the Cox Hazard Ratio: A Targeted Learning Approach to Survival Analysis in a Cardiovascular Outcome Trial Application.
3. From Logic-Respecting Efficacy Estimands to Logic-Ensuring Analysis Principle for Time-to-Event Endpoint in Randomized Clinical Trials with Subgroups.
4. Power and Sample Size Calculations for the Restricted Mean Time Analysis of Prioritized Composite Endpoints.
5. Combined Tests Based on Restricted Mean Time Lost for Competing Risks Data.
6. Composite Endpoints in Cardio-Renal Clinical Outcome Trials.
7. Robust Design and Analysis of Clinical Trials With Nonproportional Hazards: A Straw Man Guidance From a Cross-Pharma Working Group.
8. Using Surrogate Endpoints in Adaptive Designs with Delayed Treatment Effect.
9. Two-Stage Adaptive Design for Prognostic Biomarker Signatures With a Survival Endpoint.
10. Statistical Considerations for Sequential Analysis of the Restricted Mean Survival Time for Randomized Clinical Trials.
11. Statistical Assessment of Biosimilarity Based on the Relative Distance Between Follow-on Biologics for Time-to-Event Endpoints.
12. Alternative Analysis Methods for Time to Event Endpoints Under Nonproportional Hazards: A Comparative Analysis.
13. Interim Monitoring for Futility in Clinical Trials With Two Co-Primary Endpoints Using Prediction.
14. Rejoinder to Commentaries on "Estimands for Recurrent Event Endpoints in the Presence of a Terminal Event".
15. Regulatory Experience of Qualifying Total Kidney Volume as a Prognostic Biomarker for Clinical Trial Enrichment.
16. Difference in Restricted Mean Survival Time: Small Sample Distribution and Asymptotic Relative Efficiency.
17. Adaptive Informational Design of Confirmatory Phase III Trials With an Uncertain Biomarker Effect to Improve the Probability of Success.
18. Current Statistical Challenges in Oncology Clinical Trials in the Era of Targeted Therapy.
19. Rejoinder to Letter to the Editor "The Hazards of Period Specific and Weighted Hazard Ratios".
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