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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 (Jun 2026). This Phase 1 trial studies PVX7 for cervical cancer.

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

Treatments studied

Other

PVX7

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)

Demographics

Female only

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

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06315257 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received surgical resection and radiation therapy.

What disease stage is eligible?

Stage IIA or IIB or IIIA or IIIB or IVA is required.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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