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Comparison of three sample size estimation methods for non-inferiority vaccine trials with multiple continuous co-primary endpoints
Joint Event on 31st Euro Global Summit and Expo on Vaccines & Vaccination & 4th World Congress and Exhibition on Antibiotics and Antibiotic Resistance
June 14-16, 2018 Barcelona, Spain

Yang Jiaying

Southeast University, China

Posters & Accepted Abstracts: J Vaccines Vaccin

Abstract:

Combination vaccines have been extensively used for decades and bring together the issue of intersection-union. To make up for the reduction in statistical power at the study level, researchers have to increase the study sample size. In view of the nature of immunogenicity variables, we use the geometric mean concentration of immune response after vaccination as immunologic endpoint and compare three sample size calculation methods: the inflation factors method; the incrementing method and; the Bonferroni correction method when there are multiple continuous co-primary endpoints. The parameters are set according to the actual situation of combination vaccines and the simulation results were used as reference. The present study demonstrates that the incrementing method, the Bonferroni corrected method and the inflation factors method are all available when the effect size of each endpoint is comparable and there is no or weak correlation between each endpoint. When there is a valid difference of effect sizes among endpoints, the incrementing method performs better. yang_jy@foxmail.com