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CPS2028 Ayon M.
                  been  established  that  such  ethical  gain  prevails  without  significantly
                  compromising on the statistical power of the Wald test for the difference in
                  the  partial  likelihood  based  covariate-adjusted  treatment  effects.  Extensive
                  simulation studies have established that the balance between ethical gain and
                  statistical efficiency in estimating treatment effects is achieved most with the
                  CARA  design  using  the  doubly-adaptive  biased  coin  design.  However,  the
                  efficient  randomised  adaptive  design  works  best  if  the  variability  of  the
                  allocation procedure is the sole criterion for evaluation.
                      The  mertis  of  the  proposed  designs  have  also  been  highlighted  by
                  redesigning an existing clinical trial from Sverdlov, Rosenberger and Ryeznik
                  (2013), which is intended to be discussed during the talk in the congress.

                  References
                  1.  Hu, F. and Zhang, L-X. (2004), Asymptotic properties of doubly-adaptive
                      biased coin designs for multitreatment clinical trials, The Annals of
                      Statistics 32, 268–301.
                  2.  Hu, F., Zhang, L-X, and He, X. (2009). Efficient randomized adaptive
                      designs, The Annals of Statistics 37, 2543–2560.
                  3.  Rosenberger, W.F. and Sverdlov, O. (2008), Handling covariates in the
                      design of clinical trials, Statistical Science 23, 404–419.
                  4.  Rosenberger, W.F., Vidyashankar, A.N., and Agarwal, D.K. (2001),
                      Covariate-adjusted response-adaptive designs for binary response,
                      Journal of Biopharmaceutical Statistics 11, 227–236.
                  5.  Sverdlov, O., Rosenberger, W.F., and Ryeznik, Y. (2013), Utility of
                      covariate-adjusted response-adaptive randomization in survival trials.
                      Statistics in Biopharmaceutical Research 5,38–53.





























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