Clinical trial

To Test 2 Doses of GSK Biologicals' Oral Live Attenuated Human Rotavirus (HRV)…

NCT00140686 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00140686
Title To Test 2 Doses of GSK Biologicals' Oral Live Attenuated Human Rotavirus (HRV) Vaccine in Healthy Infants in Co-administration With Specific Childhood Vaccines
Official title A Multi-country & Multi-center Study to Assess the Efficacy, Safety & Immunogenicity of 2 Doses of GSK Biologicals' Oral Live Attenuated Human Rotavirus (HRV) Vaccine in Healthy Infants in Co-administration With Specific Childhood Vaccines
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Infections, Rotavirus
Intervention type Biological
Interventions Rotavirus (vaccine)
Enrollment 3,994
Start date Sep 1, 2004
Primary completion Aug 1, 2006
Completion Aug 1, 2006
First posted Sep 1, 2005
Last update posted Mar 23, 2017
Countries Czechia, Finland, France, Germany, Italy, Spain

At a glance

  • 100–999 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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