Clinical trial

Study Evaluating Persistence of Anti-HBs Antibodies in Uraemic Patients…

NCT00445185 · Henogen, Industry · Completed

Key facts

NCT number NCT00445185
Title Study Evaluating Persistence of Anti-HBs Antibodies in Uraemic Patients Receiving Henogen's HBV Vaccine, or Fendrix™
Official title A Study to Evaluate the Persistence of Anti-HBs Antibodies at Months 12, 24 and 36 in Pre-dialysis or Dialysis Patients Who Have Received a Primary Vaccination Course of Either Henogen's HBV Vaccine, HB-AS02V or GSK Biological's Fendrix™
Lead sponsor Henogen, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Hepatitis B
Intervention type Biological
Interventions Henogen HB vaccine, Fendrix vaccine
Enrollment 102
Start date Mar 1, 2007
Primary completion Jul 1, 2009
Completion Nov 1, 2009
First posted Mar 8, 2007
Last update posted Nov 19, 2009
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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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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