drugset / Trial / NCT00445185

Study Evaluating Persistence of Anti-HBs Antibodies in Uraemic Patients Receiving Henogen's HBV Vaccine, or Fendrix™

NCT00445185

Phase 3 Completed 102 enrolled Henogen
RandomizedParallel-groupOpen-labelPrevention

Summary

The current extension study will assess the persistence of anti-HBs antibodies at Months 12, 24 and 36 after primary vaccination with Henogen's HBV vaccine or Fendrix™. This protocol posting deals with the objectives \& outcome measures of the extension phase at Months 12, 24 and 36. The objectives \& outcome measures of the primary phase are presented in a separate protocol posting (NCT00291941).

Timeline

Start
2007-03
Primary completion
2009-07
Completion
2009-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Fendrix Vaccine
Subject HB-AS02 Vaccine