This is a phase I clinical study that aims to assess the safety and immunogenicity of a novel, escalating dose regimen of R21/Matrix-M™ in healthy, malaria-naïve adults.
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Safety of R21/Matrix-Mâ„¢ administered in an escalating dose, multi prime vaccination schedule versus a standard prime-boost regimen in healthy UK adults, measured by the number of solicited adverse events in each group
Timeframe: 7 days post-vaccination
Safety of R21/Matrix-Mâ„¢ administered in an escalating dose, multi prime vaccination schedule versus a standard prime-boost regimen in healthy UK adults, measured by the number of unsolicited adverse events and laboratory adverse events in each group
Timeframe: 28 days post-vaccination.
Safety of R21/Matrix-Mâ„¢ administered in an escalating dose, multi prime vaccination schedule versus a standard prime-boost regimen in healthy UK adults, measured by the number of serious adverse events in each group
Timeframe: For the follow-up period of the study, between 1-2 years
Humoral immunogenicity of R21/Matrix-Mâ„¢ administered in an escalating dose, multi-prime vaccination schedule verus a standard prime-boost regimen in healthy UK adults
Timeframe: For the follow-up period of the study, between 1-2 years