drugset / Trial / NCT01353703
Immunogenicity and Safety Study in Infants of GlaxoSmithKline Biologicals' Infanrix Hexa™ (DTPa-HBV-IPV/Hib) Vaccine
RandomizedParallel-groupOpen-labelPrevention
Summary
This study evaluates the immunogenicity and safety of Infanrix hexa™ (DTPa-HBV-IPV/Hib) when administered as a primary vaccination course to Indian infants according to a 6-10-14 weeks or a 2-4-6 months schedule.
Timeline
- Start
- 2012-04-16
- Primary completion
- 2013-02-25
- Completion
- 2013-02-25
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Infanrix hexa | Vaccine | — | Intramuscular |