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OncoMatch/Clinical Trials/NCT06315257

A Clinical Trial to Assess PVX7 Immunotherapy Regimens in Advanced Cervical Cancer Patients

Is NCT06315257 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies PVX7 for cervical cancer.

Phase 1RecruitingSidney Kimmel Comprehensive Cancer Center at Johns HopkinsNCT06315257Data as of May 2026

Treatment: PVX7A Feasibility Trial of PVX7 vaccine in advanced cervical cancer patients who have completed primary definitive therapy.

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Extracted eligibility criteria

Cancer type

Cervical Cancer

Disease stage

Required: Stage IIA, IIB, IIIA, IIIB, IVA

advanced (stage IB1-IVA) cervical cancer

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Must have received: surgical resection — primary

completed primary treatment (consisting of any of the following as per NCCN guideline standard of care: surgical resection, radiation, and/or platinum-based chemotherapy) within the past 12 months

Must have received: radiation therapy — primary

completed primary treatment (consisting of any of the following as per NCCN guideline standard of care: surgical resection, radiation, and/or platinum-based chemotherapy) within the past 12 months

Must have received: platinum-based chemotherapy — primary

completed primary treatment (consisting of any of the following as per NCCN guideline standard of care: surgical resection, radiation, and/or platinum-based chemotherapy) within the past 12 months

Lab requirements

Blood counts

white blood cell count ≥ 3,000; lymphocyte number ≥ 500; absolute neutrophil count ≥ 1,000; platelets ≥ 90,000; hemoglobin ≥ 9

Kidney function

creatinine < 1.5 X ULN or estimated creatinine clearance ≥ 60 ml/min per Modified Cockcroft-Gault Formula

Liver function

total bilirubin <1.5 X ULN, <3 x ULN if Gilbert's disease; AST/ALT <3 X ULN

Adequate organ function as defined by the following parameters: white blood cell count ≥ 3,000; lymphocyte number ≥ 500; absolute neutrophil count ≥ 1,000; platelets ≥ 90,000; hemoglobin ≥ 9; total bilirubin <1.5 X ULN, <3 x ULN if Gilbert's disease; AST/ALT <3 X ULN; creatinine < 1.5 X ULN or estimated creatinine clearance ≥ 60 ml/min per Modified Cockcroft-Gault Formula

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • The University of Alabama at Birmingham · Birmingham, Alabama
  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Baltimore, Maryland

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