RecruitingPhase 2NCT05799144

pBI-11 & TA-HPV (With Pembrolizumab as Treatment for Patients w/Advanced, PD-L1 CPS≥1, hrHPV+ Oropharyngeal Cancer

An Open-Label Phase II Clinical Trial Assessing the Safety, Feasibility, Efficacy and Immunological Correlates of Heterologous Prime-Boost With pBI-11 (IM) and TA-HPV (IM) Combined With Pembrolizumab as Treatment for Patients With Advanced, PD-L1 CPS≥1, hrHPV+ Oropharyngeal Cancer


Sponsor

Michael K. Gibson

Enrollment

54 participants

Start Date

May 16, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II trial tests how well pB1-11 and human papillomavirus tumor antigen (TA-HPV) vaccines in combination with pembrolizumab work in treating patients with oropharyngeal cancer that has come back (recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic) and that is PD-L1 and human papillomavirus (HPV) positive. Oropharyngeal cancer is a type of head and neck cancer involving structures in the back of the throat (the oropharynx), such as the non-bony back roof of the mouth (soft palate), sides and back wall of the throat, tonsils, and back third of the tongue. Scientists have found that some strains or types of a virus called HPV can cause oropharyngeal cancer. pBI-11 is a circular deoxyribonucleic acid (DNA) (plasmid) vaccine that promotes antibody, cytotoxic T cell, and protective immune responses. TA-HPV is an investigational recombinant vaccina virus derived from a strain of the vaccina virus which was widely used for smallpox vaccination. Vaccination with this TA-HPV vaccine may stimulate the immune system to mount a cytotoxic T cell response against tumor cells positive for HPV, resulting in decreased tumor growth. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread by inhibiting the PD-1 receptor. These investigational vaccines could cause or enhance an immune response in the body against HPV, during which time the activity of pembrolizumab against oropharyngeal cancer associated with HPV may be strengthened. These drugs in combination may be more effective in increasing the ability of the immune system to fight oropharyngeal cancer than pembrolizumab alone.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two vaccine-based therapies (pBI-11 and TA-HPV, which target HPV proteins) together with pembrolizumab (a standard immunotherapy drug) in patients with HPV-positive oropharyngeal cancer (throat cancer caused by HPV) that has returned or spread. **You may be eligible if...** - You are 18 or older - You have been diagnosed with recurrent or metastatic HPV-positive (p16+) oropharyngeal cancer that has not been previously treated for recurrence - Your tumor expresses PD-L1 (CPS score ≥1, a marker that indicates likely response to immunotherapy) - You are planned to start pembrolizumab as standard care - You have a good performance status (ECOG 0–1) **You may NOT be eligible if...** - Your cancer is not p16+ or does not have PD-L1 expression (CPS <1) - You have already received treatment for recurrent/metastatic disease - Other health or prior treatment criteria apply Talk to your doctor to see if this trial is right for you.

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

BIOLOGICALDNA Vaccine

Given pBI-11 IM

BIOLOGICALHuman Papillomavirus Tumor Antigen Vaccine

Given into a muscle

BIOLOGICALPembrolizumab

Given into vein

PROCEDUREComputed Tomography (CT)

Undergo a CT

PROCEDUREMagnetic Resonance Imaging (MRI)

Undergo an MRI

PROCEDUREMagnetic Resonance Imaging

Undergo blood sample collection

PROCEDUREBiopsy

Undergo tumor biopsy


Locations(2)

University of Alabama Birmingham

Birmingham, Alabama, United States

Vanderbilt University/Ingram Cancer Center

Nashville, Tennessee, United States

View Full Details on ClinicalTrials.gov

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NCT05799144