Bayesian Adaptive Randomization with Posterior Probability

This application is developed by: J. Jack Lee, Ying-Wei Kuo and Nan Chen

Department of Biostatistics, MD Anderson Cancer Center, Houston, TX 77030

PID:948; v2.0.2.0 ; Last Updated: 07/22/2020

Simulation

One Trial

Operating Characteristics

One Trial

Graph Parameters:
Arm
Color
Line Type
Point Symbol

Operating Characteristics

Graph Parameters:
Arm
Color
Line Type
Point Symbol



Animation Settings:
Note: Arm 1 is the control arm

Prior Settings:
Prior distribution for \(\theta\): \(\textit{Beta}\)(\(a_1, b_1\))
Prior distribution for \(\theta_i\): \(\textit{Beta}\)(\(a_i, b_i\))
Arm
a
b

True Response Rate:
Arm
True Rate
Sample Size:
Cohort Specification for Interim Analysis:
Randomization Parameters:
AR Cohort size is too large, suggest to use a small value.
Adaptive Randomization Tuning Parameter (\(\tau\))
Allocation Function Parameter (\(\tau\)) (0.0--1.0)
Simulation Parameters:
Efficacy Parameters:
Probability of Response (\(\theta\))
Criterion for futility stopping:
Stop for futility if \(\textit{Prob}\) (\(\theta \le \theta_{fut}\)) \(> P_{fut}\)
Stop for futility if \(\textit{Prob}\) (\(\theta \le \theta_{1}\)) \(> P_{fut}\)

Criterion for declaring efficacy early:
Stop for efficacy if \(\textit{Prob}\) (\(\theta > \theta_{eff}\)) \(\ge P_{eff}\)
Stop for efficacy if \(\textit{Prob}\) (\(\theta > \theta_{1}\)) \(\ge P_{eff}\)

Criterion for declaring efficacy:
Declare efficacy if \(\textit{Prob}\) (\(\theta > \theta_{eff.final}\)) \(\ge P_{eff.final}\)
Declare efficacy if \(\textit{Prob}\) (\(\theta > \theta_{1}\)) \(\ge P_{eff.final}\)
Note: Please only upload the file generated by this app. Do NOT edit the file.


Save Input into a csv file

Download Simulation - One Trial PDF Report
Download Simulation - One Trial Excel Report

Note: Please only upload the file generated by this app. Do NOT edit the file.




Save Input into a csv file

Download PDF Report
Download EXCEL Report

Trial Monitoring

Session 1

Note: Arm 1 is the control arm
Seq. No.
Patient ID (Optional)
Arm
Resp. Outcome






Save Trial Monitoring Input into a csv file

Download Trial Monitoring PDF Report
Download Trial Monitoring Excel Report

Support Document