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Condition Guide

New Treatments & Clinical Trials for Human Papillomavirus Infection

Last updated September 2026Data from ClinicalTrials.gov144 active trials
← Browse all Human Papillomavirus Infection trials

Human papillomavirus infection is extremely common — most sexually active people get it at some point. Most infections clear on their own within two years, but some high-risk HPV types can cause cervical cancer, head and neck cancers, and other cancers. Vaccination prevents infection, and regular screening catches cervical changes early.

What's actually going on in research

Trials are testing therapeutic vaccines that help the immune system clear persistent HPV infections, immune checkpoint inhibitors for HPV-related cancers, and combination approaches pairing vaccines with immunotherapy. Researchers are also studying better screening methods, treatment for pre-cancerous cervical changes, and ways to identify who's at highest risk for cancer.

Therapeutic vaccines

Unlike preventive HPV vaccines, therapeutic vaccines aim to treat existing infections by training the immune system to recognize and destroy infected cells. Several are in trials for cervical pre-cancer and HPV-related cancers.

Immunotherapy combinations

Checkpoint inhibitors like pembrolizumab are approved for some HPV-related cancers. Trials are testing them earlier in treatment and combining them with therapeutic vaccines or chemotherapy.

Screening advances

Studies are testing self-collection methods for HPV screening and DNA tests that predict which infections will progress to cancer. Better risk stratification could reduce unnecessary procedures.

What to know before you search

Eligibility typically depends on HPV type, whether infection has caused cellular changes or cancer, site of disease, and prior treatments.

What types of trials are currently open

  • Therapeutic vaccine trials — Testing vaccines designed to clear persistent HPV infections or treat pre-cancerous changes in the cervix or other sites.
  • Immunotherapy trials — Testing checkpoint inhibitors and other immune drugs for HPV-related cancers of the cervix, throat, anus, and other sites.
  • Treatment trials for pre-cancer — Testing less invasive treatments for cervical intraepithelial neoplasia, such as topical medications or targeted ablation.
  • Screening and prevention studies — Testing new HPV tests, self-collection methods, and ways to predict which infections need treatment.
  • Observational studies — Following people with HPV to understand why some infections clear and others persist, and what factors increase cancer risk.

Recently added Human Papillomavirus Infection trials

RecruitingInterventional study

C2001P-CS6: Testing the Feasibility of Different HPV Screening and Care Strategies for Women Living With HIV

The overall goal of this study is to inform the design and establish feasibility for a future clinical trial to determine the optimal management of women living with HIV (WLWH) with high-risk human papillomavirus (hrHPV) detected on HPV-based cervical cancer screening. WLWH have a higher diversity of anogenital HPV types causing cervical high-grade squamous intraepithelial lesions (hHSIL) and invasive cancer compared to women without HIV. While there is consensus that women testing positive for HPV 16 and/or 18 should be immediately managed and treated, optimal management strategies for women with other hrHPV types (non-16/18) are not well defined. This prospective cohort study will enroll WLWH undergoing cervical cancer screening using primary HPV testing. Women will self-collect vaginal specimens for hrHPV testing using the Abbott Alinity m HPV assay, which provides extended HPV genotyping and a proxy for HPV viral load based on cycle threshold (CT) values. Women with hrHPV detected will return for further evaluation and treatment as indicated. A subset of women will return at Month 6 for repeat evaluation. The study will evaluate feasibility for a future trial by examining recruitment, retention, return for evaluation, and completion of treatment. It will also explore management strategies for women with non-16/18 hrHPV based on extended genotyping and HPV viral load compared to standard of care approaches using visual inspection with acetic acid (VIA).

Nairobi, Kenya
RecruitingObservational study

Share your story about living with HPV infection

This qualitative phenomenological study aims to explore the lived experiences of women diagnosed with human papillomavirus (HPV) infection. The study will examine women's emotional responses to the diagnosis, its perceived effects on daily life, sexual life and partner relationships, their experiences of disclosing the diagnosis, and their information and support needs. Eligible women diagnosed with HPV infection will participate in individual semi-structured interviews. The interview data will be analyzed thematically to identify common themes reflecting participants' experiences and perceptions.

Bilecik, Bilecik, Turkey (Türkiye)
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