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Study identifier: NCT05639972 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

E7 T-cell Receptor (TCR) -T Cell Induction Therapy for Locoregionally Advanced HPV-associated Cancers

Condition: HPV-Associated Cervical Carcinoma · HPV-Related Carcinoma · HPV-Related Malignancy  ·  Sponsor: Christian Hinrichs

PhasePhase 1/Phase 2
Planned participants15
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this study is to determine the feasibility of administration of a single dose of E7 TCR-T cells as induction therapy prior to definitive treatment (chemoradiation or surgery) of locoregionally advanced HPV-associated cancers. The intent of E7 TCR-T cell treatment is to shrink or eliminate tumors and thereby facilitate definitive therapy and increase overall survival. This study seeks to determine 1) if E7 TCR-T cells can be administered without undue delay in definitive treatment, 2) the tumor response rate to E7 TCR-T cell treatment, and 3) the disease-free survival rate at 2 and 5 years. Participants will undergo an apheresis procedure to obtain T cells that will be genetically engineered to generate E7 TCR-T cells. They will receive a conditioning regimen, a single infusion of their own E7 TCR-T cells, and adjuvant aldesleukin. Participants will follow up to assess safety and determine tumor response and will return to their primary oncology team for definitive therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Tobi Adewale  ·  732-710-2406  ·  olutobi@cinj.rutgers.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Rutgers Cancer InstituteNew Brunswick, New Jersey, United StatesRecruiting
RWJBarnabas Health - Robert Wood Johnson University HospitalNew Brunswick, New Jersey, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05639972