Title | Immunogenicity and safety of porcine circovirus-free human rotavirus vaccine in healthy infants: a phase III, randomized trial. | ||
Author | Salamanca de la Cueva, Ignacio; Pahud, Barbara; Huang, Li-Min; Leonardi, Michael; Garcia-Sicilia, Jose; Cespedes, Javier; Abdelnour, Arturo; Tamura, Tsuyoshi; Kuroki, Haruo; Chiu, Nan-Chang; Virta, Miia; Kokko, Satu; Horn, Michael; Panzer, Falko; Kim, Jong-Hyun; Jin, Lee; Moerman, Leentje; Debacq, Christophe; Parra, Jose; Ugarte, Ana; Bi, Dan | ||
Journal | J Infect Dis | Publication Year/Month | 2020-May |
PMID | 32365189 | PMCID | PMC9200154 |
Affiliation + expend | 1.Instituto Hispalense de Pediatria, Sevilla, Spain. |
BACKGROUND: Porcine circovirus type 1 (PCV-1) material was detected in the human rotavirus vaccine (HRV) in 2010. In this study (NCT02914184) we compared immunogenicity and safety of the PCV-free HRV vaccine (PCV-free HRV) with HRV. PCV-free HRV is an HRV with no detection of PCV-1 and PCV-2 according to the limit of detection of the tests used. METHODS: Healthy infants 6-12 weeks of age were randomized (1:1:1:1) to receive 2 doses of 1 of the 3 lots of PCV-free HRV or HRV. The study objectives were to demonstrate lot-to-lot consistency of the PCV-free HRV and non-inferiority of PCV-free HRV as compared to HRV in terms of immunogenicity, 1-2 months post-dose 2. Reactogenicity and safety were also assessed. RESULTS: Overall, 1612 infants were enrolled and 1545 completed the study. Study objectives were demonstrated since the pre-defined criteria were met. Among participants receiving PCV-free HRV and HRV, 79.27% and 81.76% seroconverted and geometric mean concentrations were 159.5 and 152.8 U/mL, respectively. The incidences of adverse events and serious adverse events were similar between the pooled PCV-free HRV and HRV groups. CONCLUSIONS: The 3 PCV-free HRV lots demonstrated consistency and PCV-free HRV was non-inferior compared to HRV in terms of immunogenicity.