OncoMatch/Clinical Trials/NCT03913117
Study of Treatment for HPV16+ ASC-US or LSIL
Is NCT03913117 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including pNGVL4aCRTE6E7L2 and TA-CIN for asc-us.
Treatment: pNGVL4aCRTE6E7L2 · TA-CIN — Phase I clinical trial to assess safety of pNGVL4aCRTE6E7L2 DNA and TA-CIN protein vaccinations, and to seek the appropriate dose of the pNGVL4aCRTE6E7L2 DNA vaccine
Check if I qualifyExtracted eligibility criteria
Biomarker criteria
Required: HPV16 positive
Disease stage
Excluded: Stage CIN2+
Prior therapy
Cannot have received: HPV vaccine
Prior vaccination with any HPV antigen (prophylactic or therapeutic)
Cannot have received: LEEP or cervical conization procedure
Patients who have had a prior LEEP or cervical conization procedure
Lab requirements
Blood counts
White blood cell count > 3,000; Absolute lymphocyte number > 500; Absolute neutrophil count > 1,000; Platelets > 90,000; Hemoglobulin > 9
Kidney function
Creatinine < 2.5X the institutional limit of normal
Liver function
Total bilirubin <3 X the institutional limit of normal; AST(SGOT)/ALT(SGPT) <3 X the institutional limit of normal
Patients must have adequate organ function at the time of enrollment as defined by the following parameters: White blood cell count > 3,000; Absolute lymphocyte number > 500; Absolute neutrophil count > 1,000; Platelets > 90,000; Hemoglobulin > 9; Total bilirubin <3 X the institutional limit of normal; AST(SGOT)/ALT(SGPT) <3 X the institutional limit of normal; Creatinine < 2.5X the institutional limit of normal
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- UAB | The University of Alabama at Birmingham · Birmingham, Alabama
- Johns Hopkins University · Baltimore, Maryland
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
Could you qualify for this trial?
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