Mercedes Macias Parra1, Angela Gentile2, Jorge Alejandro Vazquez Narvaez3, Alejandro Capdevila4, Angel Minguez5, Monica Carrascal6, Arnold Willemsen7, Chiranjiwi Bhusal8, Daniela Toneatto9. 1. Instituto Nacional de Pediatría, Insurgentes Cuicuilco, 04530 Mexico City, Mexico. Electronic address: mermacpar@hotmail.com. 2. Hospital de Niños "Ricardo Gutiérrez", Gallo 1330, Ciudad Autónoma de Buenos Aires, Argentina. Electronic address: angelagentile@fibertel.com.ar. 3. Asociacion de Investigacion Pediatrica Y Adultos (AINPAD A.C.), Montaña Monarca No 31 Consultorio 209 y 2010 Col Jesús del Monte Morelia, Michoacán CP58350, Mexico. Electronic address: jorge.vazquez@ainpad.com.mx. 4. Paideia, Investigacion Clinica en Pediatria, Salguero 2835, Ciudad Autónoma de Buenos Aires, Argentina. Electronic address: vax_ar@yahoo.com. 5. Hospital Nuestra Señora de la Misericordia del Nuevo Siglo, Belgrano 1502, 5000 Córdoba, Argentina. Electronic address: angelminguez04@yahoo.com.ar. 6. CAIMED Investigación en Salud S.A de C.V, Calle de Manzanillo # 100 Colonia Roma Sur, Piso 2 Delegación Cuauhtémoc, México City, Mexico. Electronic address: monica.carrascal@caimed.com. 7. Plus100 B.V. c/o GSK, Hullenbergweg 83-85, 1101 CL Amsterdam, the Netherlands. Electronic address: arnold.x.willemsen@gsk.com. 8. GSK, Via Fiorentina, 1, 53100 Siena, Italy. Electronic address: chiranjiwi.x.bhusal@gsk.com. 9. GSK, Via Fiorentina, 1, 53100 Siena, Italy. Electronic address: daniela.x.toneatto@gsk.com.
Abstract
BACKGROUND: Invasive meningococcal disease has its highest incidence in infants. Co-administration of serogroup B (4CMenB) and quadrivalent conjugate (MenACWY-CRM) vaccines could protect against 5 clinically-relevant meningococcal serogroups. METHODS: This phase 3b, open, multicenter study (NCT02106390), conducted in Mexico and Argentina, enrolled and randomized (1:1:1) 750 healthy infants to receive either4CMenB co-administered with MenACWY-CRM (4CMenB/MenACWY group), 4CMenB (4CMenB group), or MenACWY-CRM alone (MenACWY group) at ages 3, 5, 7 and 13 months. Non-inferiority of immune responses of co-administration to single administration of vaccines was assessed at 1 month post-booster dose (primary objective). Immunogenicity was evaluated pre- and 1 month post-primary and booster vaccinations using human serum bactericidal assay (hSBA). Safety was assessed. RESULTS: At 1 month post-booster vaccination, between-group hSBA geometric mean titer (GMT) ratios ranged from 0.89 to 1.03 for serogroup B strains (group 4CMenB/MenACWY over 4CMenB), and from 1.05 to 2.48 for ACWY serogroups (group 4CMenB/MenACWY over MenACWY). The lower limit of the 2-sided 95% confidence intervals for all GMT ratios was >0.5; the primary objective was demonstrated. Across all groups and serogroup B strains, 68-100% and 87-100% of children had hSBA titers ≥5 at 1 month post-primary and booster vaccination, respectively. For serogroups ACWY, ≥96% (post-primary vaccination) and ≥98% (post-booster vaccination) of children in all groups had hSBA titers ≥4. Post-booster vaccination, GMTs increased ≥5.99-fold from pre-booster values for each strain/serogroup. Solicited adverse events (AEs) were more frequent in groups 4CMenB/MenACWY and 4CMenB than in MenACWY; incidence of all other AEs was similar between groups. Serious AEs were reported for 6, 13, and 11 participants in groups 4CMenB/MenACWY, 4CMenB, and MenACWY, respectively; 1 (group 4CMenB) was considered vaccine-related. CONCLUSION: Immune responses elicited by co-administration of 4CMenB and MenACWY-CRM was non-inferior to single immunization. Co-administration of vaccines was immunogenic and well tolerated in infants. ClinicalTrials.gov: NCT02106390.
RCT Entities:
BACKGROUND: Invasive meningococcal disease has its highest incidence in infants. Co-administration of serogroup B (4CMenB) and quadrivalent conjugate (MenACWY-CRM) vaccines could protect against 5 clinically-relevant meningococcal serogroups. METHODS: This phase 3b, open, multicenter study (NCT02106390), conducted in Mexico and Argentina, enrolled and randomized (1:1:1) 750 healthy infants to receive either 4CMenB co-administered with MenACWY-CRM (4CMenB/MenACWY group), 4CMenB (4CMenB group), or MenACWY-CRM alone (MenACWY group) at ages 3, 5, 7 and 13 months. Non-inferiority of immune responses of co-administration to single administration of vaccines was assessed at 1 month post-booster dose (primary objective). Immunogenicity was evaluated pre- and 1 month post-primary and booster vaccinations using human serum bactericidal assay (hSBA). Safety was assessed. RESULTS: At 1 month post-booster vaccination, between-group hSBA geometric mean titer (GMT) ratios ranged from 0.89 to 1.03 for serogroup B strains (group 4CMenB/MenACWY over 4CMenB), and from 1.05 to 2.48 for ACWY serogroups (group 4CMenB/MenACWY over MenACWY). The lower limit of the 2-sided 95% confidence intervals for all GMT ratios was >0.5; the primary objective was demonstrated. Across all groups and serogroup B strains, 68-100% and 87-100% of children had hSBA titers ≥5 at 1 month post-primary and booster vaccination, respectively. For serogroups ACWY, ≥96% (post-primary vaccination) and ≥98% (post-booster vaccination) of children in all groups had hSBA titers ≥4. Post-booster vaccination, GMTs increased ≥5.99-fold from pre-booster values for each strain/serogroup. Solicited adverse events (AEs) were more frequent in groups 4CMenB/MenACWY and 4CMenB than in MenACWY; incidence of all other AEs was similar between groups. Serious AEs were reported for 6, 13, and 11 participants in groups 4CMenB/MenACWY, 4CMenB, and MenACWY, respectively; 1 (group 4CMenB) was considered vaccine-related. CONCLUSION: Immune responses elicited by co-administration of 4CMenB and MenACWY-CRM was non-inferior to single immunization. Co-administration of vaccines was immunogenic and well tolerated in infants. ClinicalTrials.gov: NCT02106390.