CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 26 enrolled / 26 target
Drug / intervention
PRGN-2009 +6 morebiological
Likely dose
Pembrolizumab 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05996523
NCT05996523Phase 2ActiveUpdate Overdue (0.8/mo)Completion was 13mo ago

Phase II Trial of Immunotherapeutic HPV Vaccine PRGN-2009 With Pembrolizumab Before Standard Treatment in Subjects With Newly Diagnosed HPV-Associated Oropharyngeal Cancer

National Cancer Institute (NCI)·interventional·Posted Aug 18, 2023·Updated Jun 23, 2026

In Brief

A Phase 2 clinical trial evaluating PRGN-2009, Pembrolizumab, and 5 other interventions for Oropharyngeal Squamous Cell Carcinoma (SCC). Active but no longer recruiting, targeting 26 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

Background: Cancers in and around the mouth associated with human papilloma virus (HPV) are common. Two treatments (the drug pembrolizumab and the HPV vaccine PRGN-2009) have been shown to work well when used individually against these cancers. Researchers want to find out if they might work better when used together. Objective: To test pembrolizumab combined with PRGN-2009 in people with HPV-positive cancers in and around the mouth. Eligibility: Adults aged 18 and older newly diagnosed with HPV-positive cancers in and around the mouth. Design: Participants will be screened. They will have a physical exam with blood tests. They will have imaging scans. They may need to have a biopsy: A sample of tissue will be taken from the tumor. PRGN-2009 is given as an injection under the skin. Pembrolizumab is given through a tube attached to a needle inserted into a vein in the arm. Participants will have at least 3 clinic visits: At the first, they will receive both the drug and the vaccine; 15 days later, they will receive a second shot of the vaccine. At the third visit, about 1 week after the second, they will have follow-up tests. During these visits, participants will give samples of blood, urine, and saliva. Imaging scans and biopsies will be repeated. They will have tests of their heart function. Participants may opt to return for another follow-up visit about 1 month after their second dose of the vaccine. Participants will have follow-up contacts by phone 3 and 6 months after starting the study. The calls will continue once a year for 5 years.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2Active
2024202520262027202820292030
First PostedAug 18, 2023
Enrollment StartNov 7, 2023
Primary CompletionMay 22, 2025
Study CompletionJul 16, 2030
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 2.9 years ago

Arms & Interventions

Arm 1/PRGN 5x10^11 Viral Particles Subcutaneously Plus Pembrolizumab 200mg Intravenousexperimental

PRGN 5x10\^11 Viral Particles (VP) subcutaneous (SC) plus pembrolizumab 200mg intravenous (IV) as induction/ neoadjuvant therapy

Biological: PRGN-2009Drug: PembrolizumabDiagnostic Test: EKGDiagnostic Test: CTDiagnostic Test: PET scanDiagnostic Test: MRIProcedure: Biopsy

Interventions

PRGN-2009biological

PRGN-2009 5x10\^11 viral particles (VP) subcutaneously (SC) approximately two weeks apart

Pembrolizumabdrug

Pembrolizumab 200 mg intravenously (IV) concurrently with the first vaccine dose

EKGother

Baseline, completion visit, and safety follow-up visit.

CTother

Screening and baseline (neck and chest), and completion visit (neck).

PET scanother

Screening and baseline (neck and chest).

MRIother

Screening and baseline (neck and chest), and completion visit (neck).

Biopsyprocedure

Baseline and completion visit.