Optimal Sample Size for Evidence and Consensus in Phase III Clinical Trials

Author:

De Santis Fulvio,Gubbiotti Stefania

Publisher

Springer International Publishing

Reference11 articles.

1. Bittl, J.A., He, Y.: Bayesian analysis. A practical approach to interpret clinical trials and create clinical practice guidelines. Circ. Cardiovasc. Qual. Outcomes 10(8), e003563 (2017)

2. Brutti, P., De Santis, F., Gubbiotti, S.: Bayesian frequentist sample size determination: A game of two priors. Metron 72(2), 133–151 (2014)

3. CDHR/FDA: Guidance for the Use of Bayesian Statistics in Medical Device Clinical Trials. Guidance for industry and FDA staff (2010)

4. De Santis, F., Gubbiotti, S.: Joint control of consensus and evidence in Bayesian design of clinical trials. Biom. J. (2021) https://doi.org/10.1002/bimj.202100035

5. De Santis, F., Gubbiotti, S.: A dynamic power prior for Bayesian non-inferiority trials. Submitted (2021)

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