drugset / Trial / NCT01251276

Hepatitis B Challenge Dose in Adults (V232-059-10)

NCT01251276

Phase 3 Completed 204 enrolled Merck Sharp & Dohme LLC
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this trial is to describe the Seroprotection Rate (SPR) at least 2 years following completion of a primary series with a hepatitis B vaccine (Base Study V232-059, NCT00440531) and 1 month following a challenge dose with a Modified Process Hepatitis B vaccine.

Timeline

Start
2010-11-30
Primary completion
2011-04-12
Completion
2011-04-12

Drugs

EvaluationDrugModalityDoseRoute
Subject HBVAXPRO Vaccine 10 ug Intramuscular