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OncoMatch/Clinical Trials/NCT06341907

Application of MRD Combined With Personalized Vaccine in the Treatment of Postoperative Recurrence Prevention of EOC

Is NCT06341907 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2/3 trial studies Neoantigen polypeptide vaccine for epithelial ovarian cancer.

Phase 2/3RecruitingSecond Affiliated Hospital of Wenzhou Medical UniversityNCT06341907Data as of Jun 2026Location: China

Treatment: Neoantigen polypeptide vaccineThe goal of this clinical trial is as follows:(1) Establish a clinical technical system for ctDNA dynamic monitoring of MRD in postoperative EOC patients, providing a new technical means for postoperative recurrence prevention and monitoring of EOC patients.(2) Establish a clinical technical system for adjuvant treatment of postoperative recurrence prevention for EOC patients with conventional protocols combined with personalized vaccines, so as to provide a new treatment method for postoperative recurrence prevention for EOC patients, with a view to obtaining a better survival prognosis.(3) To establish and improve the prediction process of Neoantigen for ovarian cancer and the in vitro evaluation system of the effectiveness of neoantigen vaccine, achieve independent innovation of tumor neoantigen vaccine treatment technology, and cultivate a group of technical forces to master the development of modern tumor vaccine drugs.(4) The new technology system has been promoted and applied in 5 hospitals in the province.

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Extracted eligibility criteria

Treatments studied

Other

Neoantigen polypeptide vaccine

Cancer type

Ovarian Cancer

Disease stage

Required: Stage II, III, IV

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 70
Female only

Prior therapy

Cannot have received: immunotherapy

Patients who have received other immunotherapy within 1 month (such as immunotherapy with checkpoint inhibitors, therapeutic antibodies, immune cell therapy, and immune system modulator therapy)

Lab requirements

Blood counts

neutrophil count ≥1.5×109 /l; hemoglobin ≥10.0 g/dl; platelet count ≥100×109 /l

Kidney function

creatinine clearance ≥60 ml/min

Liver function

total bilirubin ≤2× uln; ast and alt ≤2× uln

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

Frequently asked questions

Is NCT06341907 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior immunotherapy disqualifies patients from enrollment.

What disease stage is eligible?

Stage II or III or IV is required.

Is there an age limit?

Yes. Patients must be 70 years or younger.

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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