A Phase III Clinical Trial to Study the Tolerability and Immunogenicity of V503 a Multivalent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine in 16- to 26-Year-Old Men and 16- to 26-Year-Old Women
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of this study is to test the safety, tolerability, and immune response of V503 in young men and women.
Description
The purpose of this study is to test the safety, tolerability, and immune response of V503 in young men and women.
Details
| Condition | HPV |
|---|---|
| Age | 16years - 26years |
| Clinical Study Identifier | TX2874 |
| Last Modified on | 19 February 2024 |
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