drugset / Trial / NCT00680914

Primary Vaccination Course in Children Receiving Pneumococcal Conjugate Vaccine GSK 1024850A or Prevenar™ and Hiberix™

NCT00680914

Phase 3 Completed 503 enrolled GlaxoSmithKline
RandomizedParallel-groupSingle-blindPrevention

Summary

The purposes of this study are: To demonstrate the immunogenicity in terms of antibody response following primary vaccination of Korean infants with the pneumococcal conjugate vaccine GSK 1024850A compared to Prevenar™ when co-administered with a Haemophilus influenzae type b (Hib) vaccine in children during the first 6 months of life. To evaluate the safety/reactogenicity in terms of solicited and unsolicited symptoms and serious adverse events following primary vaccination of Korean infants with the pneumococcal conjugate vaccine GSK 1024850A.

Timeline

Start
2008-06-10
Primary completion
2009-05-08
Completion
2009-05-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Prevnar 13 Vaccine Intramuscular
Subject Synflorix Vaccine Intramuscular
Background HAEMOPHILUS INFLUENZAE TYPE B STRAIN 20752 CAPSULAR POLYSACCHARIDE TETANUS TOXOID CONJUGATE ANTIGEN Vaccine Intramuscular