Sample Size Calculation for Two Primary Time-to-Event Endpoints in Clinical Trials

Documentation for package ‘coprimary’ version 1.0

coprimary-package	Sample size calculation for two primary time-to-event endpoints in phase III clinical trials
coprimary	Sample size calculation for two primary time-to-event endpoints in phase III clinical trials
datacheck	check the consistency of the parameters
nbevent	Number of events estimates
ncoprimary	Sample size calculation in clinical trials with two co-primary time-to-event endpoints
nsurvival	Sample size calculation in clinical trials with one primary survival endpoint
probafix	Probabitility of event when the follow-up is fixed
probanofix	Probabitility of event when the follow-up is no fixed