drugset / Trial / NCT01548118
Evaluate the Safety of Recombinant Human Papillomavirus Bivalent (Types 16 and 18) Vaccine (Yeast) in Healthy Females
RandomizedParallel-groupQuadruple-blind
Summary
This study will evaluate the safety of a novel recombinant human papillomavirus bivalent ( types 16 and 18 ) vaccine ( Yeast ) with different dose in healthy females between 9-45 years of age at enrollment.
Timeline
- Start
- 2012-02
- Primary completion
- 2012-10
- Completion
- 2012-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HPV 16/18 VLP AS04 | Vaccine | 0.5 ml | Intramuscular |
| Subject | HPV 16/18 VLP AS04 | Vaccine | 1 ml | Intramuscular |