Safety and Immunogenicity of V540B in Healthy Adults (V540B-002).
Merck Sharp & Dohme LLC · NCT06623409
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–45 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 124
- US sites recruiting
- 2
- Study start
- November 12, 2024
- Record last updated
- October 8, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Researchers are looking for new ways to prevent cancers related to human papillomavirus (HPV). HPV is a common virus that can cause an infection. There are many different types of HPV. Most people's immune system can fight HPV infection and it goes away without treatment. For some people, HPV infections can last longer and may cause cancer years later.
A standard vaccine to prevent HPV-related cancers is GARDASIL®9 (G9). G9 protects against 9 types of HPV but it does not protect against other types of HPV. The study vaccine (called V540B) is designed to protect against the same HPV types that G9 protects against plus other HPV types. The main goal of this study is to learn about the safety of V540B in healthy adults and if people tolerate it.
Being studied: GARDASIL®9 (G9); V540B
Conditions: Healthy
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
The key inclusion criteria include but are not limited to the following:
- Is in good health based on medical history, physical examination, vital sign (VS) measurements and electrocardiograms (ECGs) performed before randomization.
Exclusion Criteria
The key exclusion criteria include but are not limited to the following:
- Has a history of abnormal Pap smears, HPV- related external genital lesions (eg,condyloma acuminate, vulval intraepithelial neoplasia (VIN), or prostatic intraepithelial neoplasia (PIN)) or external genital cancer (eg, penile cancer), HPV-related vaginal or anal lesions (eg, condyloma acuminata or vaginal intraepithelial neoplasia (VaIN)) or vaginal or anal cancer.
- Has a history of cancer (malignancy).
- Has received any HPV vaccine or is expected to receive any HPV vaccine during the study, outside the protocol.
Recruiting US locations
Velocity Clinical Research, Hallandale Beach ( Site 0003)
Hallandale, FL 33009
Site contact: Study Coordinator · 954-455-5757
Research Centers of America ( Hollywood ) ( Site 0001)
Hollywood, FL 33024
Site contact: Study Coordinator · 954-324-4706
Study contacts (from the official record)
- Toll Free Number · 1-888-577-8839 · Trialsites@msd.com
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