Clinical trial

Compare the Immune Response & Safety Elicited by Henogen's Adjuvanted Hepatitis…

NCT00291954 · Henogen, Industry · Completed

Key facts

NCT number NCT00291954
Title Compare the Immune Response & Safety Elicited by Henogen's Adjuvanted Hepatitis B Vaccine vs Aventis Pasteur MSD's Hepatitis B Vaccine in Pre-Dialysis & Dialysis Patients Who Did Not Respond to Previous Hepatitis B Vaccination
Official title A Multicentric, Randomised Study Comparing the Immunogenicity and Safety of Henogen's Adjuvanted Hepatitis B Vaccine Given at 0, 1months to That of Aventis Pasteur MSD's Hepatitis B Given at 0, 1 Months in Pre-Dialysis, and Dialysis Patients Did Not Respond to Previous Hepatitis B Vaccination
Lead sponsor Henogen, Industry
Collaborators GlaxoSmithKline Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Hepatitis B
Intervention type Biological
Interventions HB-AS02V, HBVAXPRO vaccine
Enrollment 257
Start date Mar 1, 2006
Primary completion Oct 1, 2007
Completion Oct 1, 2007
First posted Feb 15, 2006
Last update posted Aug 28, 2008
Countries Belgium, Czechia, Hungary

At a glance

  • 10–99 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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