ClinTrialPredict - Predicting and Simulating Clinical Trial with Time-to-Event
Endpoint
Predict the course of clinical trial with a time-to-event
endpoint for both two-arm and single-arm design. Each of the
four primary study design parameters (the expected number of
observed events, the number of subjects enrolled, the
observation time, and the censoring parameter) can be derived
analytically given the other three parameters. And the
simulation datasets can be generated based on the design
settings.
