Adaptive Randomization for Multiarm Comparative Clinical Trials Based on Joint Efficacy/Toxicity Outcomes
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- Lanju Zhang & William F. Rosenberger, 2007. "Response‐adaptive randomization for survival trials: the parametric approach," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 56(2), pages 153-165, March.
- Peter F. Thall & Lurdes Y. T. Inoue & Thomas G. Martin, 2002. "Adaptive Decision Making in a Lymphocyte Infusion Trial," Biometrics, The International Biometric Society, vol. 58(3), pages 560-568, September.
- Ying Kuen Cheung & Peter F. Thall, 2002. "Monitoring the Rates of Composite Events with Censored Data in Phase II Clinical Trials," Biometrics, The International Biometric Society, vol. 58(1), pages 89-97, March.
- Ying Kuen Cheung & Rick Chappell, 2000. "Sequential Designs for Phase I Clinical Trials with Late-Onset Toxicities," Biometrics, The International Biometric Society, vol. 56(4), pages 1177-1182, December.
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