All subjects who agreed to follow up beyond one year of age and who complied with the study protocol were included in the supplementary analyses, regardless of event(s) in the first year of life. Vaccine efficacy against a particular event was calculated using the formula VE = (1 − relative
risk) × 100, where relative risk = cumulative incidence of the event in the vaccinated group/cumulative incidence of the event Bortezomib nmr in the placebo group. Ninety-five percent confidence intervals for vaccine efficacy were derived from the exact confidence interval for the Poisson rate ratio for each analysis [17]. A p-value was also calculated using a two-sided Fisher’s exact test. The incidence rate in a group was computed as the number of infants reporting at least one event (the first event only was included) divided by the total follow-up time for each parameter or subgroup with corresponding 95% confidence AZD6244 clinical trial intervals [18]. The number of events prevented (per 100 infants per year) was obtained as 100 times the difference in incidence rate between the group that received placebo and the group that received RIX4414. The associated confidence interval was derived using the method conceptualized by Zou and Donner [19]. The study was undertaken according to Good Clinical Practice (GCP)
guidelines. Informed consent was obtained from the subject’s parent/guardian prior to any study procedure being undertaken. In case of illiteracy of the parent/guardian, consent was undertaken with the assistance of an impartial witness. The study protocol was approved by the Malawi National Health Sciences Research Committee, the Liverpool School of Tropical Medicine Research Ethics Committee, and the ethics committee of the World Health Organisation. A total of 1773 infants were enrolled in Malawi. Of these, 1513 and 1194 infants were included in the ATP efficacy cohorts for the first and second years of follow-up, respectively (Fig. 1). Demographic details were similar for vaccine and placebo groups [14]. The mean age (SD) at final visit was 19 months (4.78) for the RIX4414 group and 18.9 Dipeptidyl peptidase months (5.03) for the placebo group. The mean duration of follow-up
was 0.6 years for the first follow-up period, 0.78 years for the second follow-up period and 1.25 years for the entire follow-up period. The incidence of severe rotavirus gastroenteritis was higher in the placebo group during the first year of follow-up (7.9%, 95% CI 5.6–10.6) than in the second year of follow-up (4.5%, 2.6–7.1) (Table 1). Fewer episodes of severe rotavirus gastroenteritis occurred in the pooled RIX4144 group compared with the placebo group for the first, second, and entire follow-up periods (VE 49.4% [19.2–68.3], 17.6% [−59.2 to 56.0] and 38.1% [9.8–57.3], respectively), although the differences were not statistically significant for the second follow-up period. For two years of follow-up, rotavirus vaccination prevented 6.
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