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Monitoring the Rates of Composite Events with Censored Data in Phase II Clinical Trials

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  • Ying Kuen Cheung
  • Peter F. Thall

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  • 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.
    • Handle: RePEc:bla:biomet:v:58:y:2002:i:1:p:89-97
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    File URL: http://hdl.handle.net/10.1111/j.0006-341X.2002.00089.x
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    References listed on IDEAS

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    1. 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.
    2. Dean A. Follmann & Paul S. Albert, 1999. "Bayesian Monitoring of Event Rates with Censored Data," Biometrics, The International Biometric Society, vol. 55(2), pages 603-607, June.
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    Cited by:

    1. Uttam Bandyopadhyay & Atanu Biswas & Rahul Bhattacharya, 2010. "A covariate‐adjusted adaptive design for two‐stage clinical trials with survival data," Statistica Neerlandica, Netherlands Society for Statistics and Operations Research, vol. 64(2), pages 202-226, May.
    2. Yuan Ji & B. Nebiyou Bekele, 2009. "Adaptive Randomization for Multiarm Comparative Clinical Trials Based on Joint Efficacy/Toxicity Outcomes," Biometrics, The International Biometric Society, vol. 65(3), pages 876-884, September.
    3. B. Nebiyou Bekele & Yisheng Li & Yuan Ji, 2010. "Risk-Group-Specific Dose Finding Based on an Average Toxicity Score," Biometrics, The International Biometric Society, vol. 66(2), pages 541-548, June.

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