Clinical trial

Safety and Immunogenicity Study of a Booster Dose of GSK Biologicals' 10-valent…

NCT00370227 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00370227
Title Safety and Immunogenicity Study of a Booster Dose of GSK Biologicals' 10-valent Pneumococcal Conjugate Vaccine
Official title To Assess Safety, Reactogenicity & Immunogenicity of a Booster Dose of Pneumococcal Conjugate Vaccine, Co-admin With GSK Biologicals' MMRV Vaccine in Children (2nd yr of Life) Primed With the Pneumococcal Conjugate Vaccine in Study 105553.
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Infections, Streptococcal
Intervention type Biological
Interventions 10 valent pneumococcal conjugate (vaccine)
Enrollment 390
Start date Oct 1, 2006
Completion Mar 1, 2007
First posted Aug 31, 2006
Last update posted Oct 28, 2016
Countries Finland

At a glance

  • 1–9 Study sites
  • No 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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