Tetravalent meningococcal serogroups A, C, W-135 and Y conjugate vaccine is well tolerated and immunogenic when co-administered with measles–mumps–rubella–varicella vaccine during the second year of life: An open, randomized controlled trial
“…MenACWY-TT aşısının çocuk, adolesan, erişkin ve 55-103 yaş arası popülasyonda da immünojenik ve güvenilir olduğu yapılan çalışmalarda gösterilmiştir (25)(26)(27)(28)(29)(30)(31)(32)(33)(34) . Baxter ve ark.…”
Section: Menacwy-tt Ile Ilgili Yürütülen Antikor Sürekliliğiunclassified
“…MenACWY-TT aşısının çocuk, adolesan, erişkin ve 55-103 yaş arası popülasyonda da immünojenik ve güvenilir olduğu yapılan çalışmalarda gösterilmiştir (25)(26)(27)(28)(29)(30)(31)(32)(33)(34) . Baxter ve ark.…”
Section: Menacwy-tt Ile Ilgili Yürütülen Antikor Sürekliliğiunclassified
“…44 A further study by Vesikari et al also showed that MenACWY-TT was non-inferior to MenC-CRM197 and was immunogenic in terms of serogroups A, W and Y when administered one thousand toddlers aged 12 to 23 months. 45 In a more recent phase III study conducted in Finland where 1303 healthy toddlers aged 12 to 18 monthsout of the 1554 enrolled -were included in the analysis, Men-ACWY-TT was found immunogenic in 100% of the subjects with hSBA titers > 1:8 and non-inferior to HibMenCY-TT for the serogroups C and Y. 46 Immunogenicity in children Knuf et al established in his study the immunogenicity of four experimental formulations of MenACWY-TT in 268 children aged 3 to 5 years and demonstrated that it was non-inferior to the tetravalent PS vaccine (Mencevax TM , GSK Biologicals).…”
Section: Immunogenicity Of Menacwy-ttmentioning
confidence: 99%
“…45 Group 1 (MMRVCACWY-TT group) received both MenACWY-TT and MMRV at visit one then a second dose of MMRV after 12 weeks, group 2 (ACWY-TT group) received MenACWY-TT at visit one followed with 2 doses of MMRV separated by 6 weeks each, group 3 (MMRV group)received MMRV at visit one then MenC-CRM197 in 6 weeks and a second dose of MMRV 6 weeks later, and group 4 (MenC group) received MenC-CRM197 followed in 6 weeks by 2 doses of MMRV separated by 6 weeks each. The primary objective was to assess the immunogenicity and safety of MenACWY-TT.…”
Introduction: Meningococcal disease is a major cause of morbidity and mortality worldwide with reported epidemics and outbreaks in different parts of the world. Despite the availability of antimicrobial therapy, challenges remain in early recognition and prevention of disease. Several vaccines have been developed to date aiming at preventing disease spread. Discussion: MenACWY-TT (Nimenrix TM ) has been extensively studied for use in different age groups. Phase II and III randomized trials have demonstrated its immunogenicity when administered in children aged 1 year and older, adolescents and adults. It has an acceptable safety profile with minor adverse events comparable to other vaccines. Follow up studies have shown persistence of protective antibodies up to three years. MenACWY-TT was safely and effectively coadministered with different recommended vaccines. Conclusion: MenACWY-TT is a safe and immunogenic vaccine that can be used to protect against these four serogroups in individuals older than 1 year of age.
“…Twenty-nine clinical trials [26][27][28][29][30][31][32][33][34][35][37][38][39][40][41][42][43][44][45][46][47][48][49][50] reported the incidence of febrile seizure or vaccine related febrile seizure within 0-28, 0-42 or 0-56 days (0-28/42/56 days) after first MMRV vaccine dose in healthy children aged 9-24 months, twenty-five of them [26][27][28][29][30][33][34][35][37][38][39][40][41][42][43][45][46][47][48][49][50] also reported the incidence within a smaller risk window of 7 to 10 days (7-10 days) after vaccination. Children in 17 clinical trials [27][28][29]…”
Section: Description Of Studies Includedmentioning
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