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Comment
. 2020 Jun;76(2):595-598.
doi: 10.1111/biom.13246. Epub 2020 Apr 6.

Discussion on "Predictively consistent prior effective sample sizes," by Beat Neuenschwander, Sebastian Weber, Heinz Schmidli, and Anthony O'Hagan

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Comment

Discussion on "Predictively consistent prior effective sample sizes," by Beat Neuenschwander, Sebastian Weber, Heinz Schmidli, and Anthony O'Hagan

Yeonhee Park et al. Biometrics. 2020 Jun.
No abstract available

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References

REFERENCES

    1. FDA (2019) Draft Guidance for Industry: Interacting with the FDA on Complex Innovative Trial Designs for Drugs and Biological Products. https://www.fda.gov/regulatory-information/search-fda-guidance-documents.... Accessed September 23, 2019.
    1. FDA (2018) Framework for FDA's real-world evidence program. https://www.fda.gov/media/120060/download. Accessed December 2018.
    1. Lee, S.M. and Cheung, Y. K. (2009) Model calibration in the continual reassessment method. Clinical Trials, 6(3), 227-238.
    1. Morita, S., Thall, P.F. and Müller, P. (2008) Determining the effective sample size of a parametric prior. Biometrics, 64(2), 595-602.
    1. Neuenschwander, B., Weber, S., Schmidli, H. and O'Hagan, A. (2020) Predictively consistent prior effective sample size. Biometrics, https://doi.org/10.1111/biom.13252.

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