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Semiparametric dose finding methods

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  • M. Clertant
  • J. O’Quigley

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Suggested Citation

  • M. Clertant & J. O’Quigley, 2017. "Semiparametric dose finding methods," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 79(5), pages 1487-1508, November.
    • Handle: RePEc:bla:jorssb:v:79:y:2017:i:5:p:1487-1508
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    File URL: http://hdl.handle.net/10.1111/rssb.12229
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    References listed on IDEAS

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    1. Suyu Liu & Ying Yuan, 2015. "Bayesian optimal interval designs for phase I clinical trials," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 64(3), pages 507-523, April.
    2. Ying Kuen Cheung & Rick Chappell, 2002. "A Simple Technique to Evaluate Model Sensitivity in the Continual Reassessment Method," Biometrics, The International Biometric Society, vol. 58(3), pages 671-674, September.
    3. Azriel, David, 2012. "A note on the robustness of the continual reassessment method," Statistics & Probability Letters, Elsevier, vol. 82(5), pages 902-906.
    4. Tian, Tian, 2016. "A note on continual reassessment method," Statistics & Probability Letters, Elsevier, vol. 113(C), pages 94-102.
    5. Ying Kuen Cheung, 2005. "Coherence principles in dose-finding studies," Biometrika, Biometrika Trust, vol. 92(4), pages 863-873, December.
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    Citations

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    Cited by:

    1. Pavel Mozgunov & Thomas Jaki, 2020. "An information theoretic approach for selecting arms in clinical trials," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 82(5), pages 1223-1247, December.
    2. Sean M. Devlin & Alexia Iasonos & John O’Quigley, 2021. "Phase I clinical trials in adoptive T‐cell therapies," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 70(4), pages 815-834, August.

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