Therapy for High-Risk HPV 16-Positive Oropharynx Cancer Patients
Part of paid clinical trials in Baltimore, Maryland.
- Sponsor
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- Study ID
- NCT04001413
- Phase
- PHASE2
- Status
- Withdrawn
Conditions
- HPV Positive Oropharyngeal Squamous Cell Carcinoma
- HPV-Related Carcinoma
- Oropharynx Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- MEDI0457 — DRUGMEDI0457 is an investigational drug that will be administered with the Cellectra Device in this study
- Durvalumab — DRUGDurvalumab is an investigational drug in this study.
Study Details
Combination immune checkpoint inhibitor and DNA vaccine will result in clearance of HPV DNA biomarkers (oral and/or plasma) for patients with persistent HPV-16 E6/E7 DNA (HPV biomarker) after treatment with curative intent.
Key Dates
- Start date
- Sep 17, 2019
- Status verified
- Jul 2022
- Primary completion
- Mar 25, 2021
- Completion
- Mar 25, 2021
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- No Intervention: Arm A: ObservationalNo intervention, observational arm.
- Experimental: Arm B: Durvalumab AloneDurvalumab will be administered as an IV Infusion.
- Experimental: Arm C: MEDI0457 and DurvalumabMEDI0457 is an injection. Durvalumab will be administered as an IV Infusion.
Primary Outcome Measure
Number of participants in whom there is clearance of Human Papiloma Virus (HPV) biomarkers post-intervention [ Time Frame: Up to 5 years ]
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Johns Hopkins University | Baltimore | Maryland | 21287 | - |
| Mount Sinai School of Medicine | New York | New York | 10029 | - |
| Mount Sinai School of Medicine, The Tisch Cancer Institute | New York | New York | 10029 | - |
| University of Pennsylvania | Philadelphia | Pennsylvania | 19104 | - |
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