Table 1.
|
|
Comments | ||
---|---|---|---|---|
|
|
The optimal dose in terms of μS was selected in phase I-II, so it is not desirable to switch doses at stage 2. In this scenario, the phase I-II/III design cannot provide an improvement over phase I-II → III. | ||
|
|
The dose selected in phase I-II is optimal in terms of ϕ but is not optimal in terms of μS. This illustrates the advantage of the phase I-II/III design over phase I-II → III design. | ||
|
|
The dose selected in phase I-II is suboptimal based on ϕ, but the optimal doses in terms of ϕ and μS are identical. This scenario illustrates the advantage of the phase I-II/III design over phase I-II → III design. | ||
|
|
The dose selected in phase I-II is suboptimal based on ϕ, but the optimal doses in terms of ϕ and μS are not identical. This scenario illustrates the advantage of the phase I-II/III design over phase I-II → III design. |