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. 2011 Jul 22;4:137–147. doi: 10.2147/IDR.S12716

Table 2.

Overview of published clinical studies of MenACWY-CRM in children and adolescents

Age group Immunogenicity among MenACWY-CRM recipients Safety and tolerability among MenACWY-CRM recipients
Infants from 2 months of age* 60%–92% of two-dose and 81%–99% of three-dose recipients had protective hSBA titers (≥4)52 Most common reactions were injection site redness and irritability52
Infants from 6 months of age 86%–100% of two-dose recipients had protective hSBA titers (≥4)54 Most common reactions were injection site redness and irritability54
Toddlers 86%–100% of two-dose primed and 94%–100% of three-dose primed toddlers had protective hSBA titers (≥4)52 Most common reactions were injection site redness and irritability52
65%–100% of unprimed toddlers had protective hSBA titers (≥4) after two doses54
Children aged 2–10 years 83%–95% of two-dose recipients had protective hSBA titers (≥4)56 Most common reactions were injection site pain, headache, and irritability56
Adolescents 75%–96% of adolescents had protective hSBA titers (≥4)58,59 Most common reactions were injection site pain and headache58,59

Note:

*

Used an adjuvant vaccine formulation.

Abbreviation: hSBA, human complement.