Clinical trial

Assess the Safety & Reactogenicity of DTPa-IPV/Hib Vaccine Administered at 3, 4…

NCT00325156 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00325156
Title Assess the Safety & Reactogenicity of DTPa-IPV/Hib Vaccine Administered at 3, 4, 5 & 18 Mths of Age, in Healthy Infants
Official title An Open, Multicentric, Post-marketing Surveillance Study to Assess the Safety and Reactogenicity of GlaxoSmithKline Biologicals' DTPa-IPV/Hib Vaccine Administered at 3, 4, 5 and 18 Months of Age, in Healthy Infants.
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Diphtheria, Tetanus, Poliomyelitis, Acellular Pertussis, Haemophilus Influenzae Type b, Diphtheria-Tetanus-aPertussis-Poliomyelitis Vaccines
Intervention type Biological
Interventions GSK Biologicals' combined DTPa-IPV/Hib vaccine
Enrollment 2,590
Start date Nov 2, 2004
Primary completion Aug 23, 2007
Completion Aug 23, 2007
First posted May 12, 2006
Last update posted Jan 2, 2020
Countries Singapore

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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