drugset / Trial / NCT01251276
Hepatitis B Challenge Dose in Adults (V232-059-10)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HBVAXPRO | Vaccine | 10 ug | Intramuscular |