Patient-Specific Dose Finding Based on Bivariate Outcomes and Covariates
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- Peter F. Thall & Leiko H. Wooten & Elizabeth J. Shpall, 2006. "A Geometric Approach to Comparing Treatments for Rapidly Fatal Diseases," Biometrics, The International Biometric Society, vol. 62(1), pages 193-201, March.
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- Alam, M. Iftakhar & Bogacka, Barbara & Coad, D. Stephen, 2017. "Pharmacokinetically guided optimum adaptive dose selection in early phase clinical trials," Computational Statistics & Data Analysis, Elsevier, vol. 111(C), pages 183-202.
- Yifei Zhang & Sha Cao & Chi Zhang & Ick Hoon Jin & Yong Zang, 2021. "A Bayesian adaptive phase I/II clinical trial design with late‐onset competing risk outcomes," Biometrics, The International Biometric Society, vol. 77(3), pages 796-808, September.
- Nadine Houede & Peter F. Thall & Hoang Nguyen & Xavier Paoletti & Andrew Kramar, 2010. "Utility-Based Optimization of Combination Therapy Using Ordinal Toxicity and Efficacy in Phase I/II Trials," Biometrics, The International Biometric Society, vol. 66(2), pages 532-540, June.
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- Xinyang Huang & Jin Xu, 2020. "Estimating individualized treatment rules with risk constraint," Biometrics, The International Biometric Society, vol. 76(4), pages 1310-1318, December.
- Beibei Guo & Ying Yuan, 2017. "Bayesian Phase I/II Biomarker-Based Dose Finding for Precision Medicine With Molecularly Targeted Agents," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 112(518), pages 508-520, April.
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