Analysis of composite endpoints with component‐wise censoring in the presence of differential visit schedules
Author:
Affiliation:
1. Division of Biostatistics University of Minnesota Minneapolis Minnesota USA
2. Department of Quantitative Health Sciences & Taussig Cancer Institute Cleveland Clinic Cleveland Ohio USA
Funder
National Cancer Institute
Publisher
Wiley
Subject
Statistics and Probability,Epidemiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/sim.9312
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4. FDA.Clinical trial endpoints for the approval of cancer drugs and biologics guidance for industry; 2018:12;https://www.fda.gov/regulatory‐information/search‐fda‐guidance‐documents/clinical‐trial‐endpoints‐approval‐cancer‐drugs‐and‐biologics.
5. Bias in progression‐free survival analysis due to intermittent assessment of progression
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