RecruitingPhase 1NCT05985681

Testing RG1-VLP Vaccine to Prevent HPV-related Cancers

A Dose Escalation Phase I Trial of the Safety and Immunogenicity of RG1-VLP, A Candidate Broadly Protective Vaccine for the Prevention of HPV-Associated Cancer


Sponsor

National Cancer Institute (NCI)

Enrollment

18 participants

Start Date

Jan 27, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This phase I trial tests the safety, side effects, and best dose of RG1-virus-like particle (VLP) in preventing human papillomavirus (HPV)-related cancers in women. RG1-VLP is a vaccine that aims to protect against rare HPV types not targeted by currently approved HPV vaccines. HPV is a common sexually-transmitted infection that can cause certain genital and oral cancers. RG1-VLP contains a protein of HPV type 16 (HPV16) with a slightly different structure than the licensed Gardasil-9 vaccine. Gardasil-9 is approved by the Federal Drug Administration to help protect against diseases caused by some types of HPV. Gardasil-9 also contains 9 different HPV proteins. Both vaccines contain alum to stimulate the immune system. The usual approach for the prevention of HPV-related cancers for patients who are at increased risk is to consider the currently approved HPV vaccine like Gardasil-9, as well as to be followed closely by their doctor to watch for the development of cancer via routine pap smears. This trial may allow researchers to find out whether the RG1-VLP vaccine can safely trigger an immune response against HPV in healthy women and if it is better or worse than the usual approach for the prevention of HPV-related cancers.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Biospecimen Collection, a biological treatment called HPV16 RG1 VLP Vaccine, and others for people with human papillomavirus-related carcinoma. The study is currently recruiting participants at 5 locations. People eligible for this study include women aged 18 Years to 60 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBiospecimen Collection

Undergo blood sample and vaginal swab collection

BIOLOGICALHPV16 RG1 VLP Vaccine

Given IM

OTHERQuestionnaire Administration

Ancillary studies

BIOLOGICALRecombinant Human Papillomavirus Nonavalent Vaccine

Given via injection


Locations(5)

University of Alabama at Birmingham Cancer Center

Birmingham, Alabama, United States

Johns Hopkins University/Sidney Kimmel Cancer Center

Baltimore, Maryland, United States

Staten Island University Hospital

Staten Island, New York, United States

University of Wisconsin Carbone Cancer Center - University Hospital

Madison, Wisconsin, United States

Medical University Vienna

Vienna, Austria

View Full Details on ClinicalTrials.gov

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NCT05985681


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