Combined criteria for dose optimisation in early phase clinical trials
Author:
Affiliation:
1. Institute of Statistical Research and TrainingUniversity of Dhaka Dhaka Bangladesh
2. School of Mathematical SciencesQueen Mary University of London London UK
Publisher
Wiley
Subject
Statistics and Probability,Epidemiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/sim.8292
Reference26 articles.
1. Bayesian Adaptive Methods for Clinical Trials
2. Seamless Phase I/II Adaptive Design for Oncology Trials of Molecularly Targeted Agents
3. A Strategy for Dose-Finding and Safety Monitoring Based on Efficacy and Adverse Outcomes in Phase I/II Clinical Trials
4. Dose-Finding Based on Efficacy-Toxicity Trade-Offs
5. An adaptive dose-finding design incorporating both toxicity and efficacy
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