Optimal sample size division in two-stage seamless designs

Pharm Stat. 2024 Nov-Dec;23(6):854-863. doi: 10.1002/pst.2394. Epub 2024 Apr 27.

Abstract

Inferentially seamless 2/3 designs are increasingly popular in clinical trials. It is important to understand their relative advantages compared with separate phase 2 and phase 3 trials, and to understand the consequences of design choices such as the proportion of patients included in the phase 2 portion of the design. Extending previous work in this area, we perform a simulation study across multiple numbers of arms and efficacy response curves. We consider a design space crossing the choice of a separate versus seamless design with the choice of allocating 0%-100% of available patients in phase 2, with the remainder in phase 3. The seamless designs achieve greater power than their separate trial counterparts. Importantly, the optimal seamless design is more robust than the optimal separate program, meaning that one range of values for the proportion of patients used in phase 2 (30%-50% of the total phase 2/3 sample size) is nearly optimal for a wide range of response scenarios. In contrast, a percentage of patients used in phase 2 for separate trials may be optimal for some alternative scenarios but decidedly inferior for other alternative scenarios. When operationally and scientifically viable, seamless trials provide superior performance compared with separate phase 2 and phase 3 trials. The results also provide guidance for the implementation of these trials in practice.

Keywords: multiple testing; seamless phase 2/3 trial; treatment selection.

MeSH terms

  • Clinical Trials, Phase II as Topic* / methods
  • Clinical Trials, Phase III as Topic* / methods
  • Computer Simulation*
  • Humans
  • Research Design*
  • Sample Size