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OncoMatch/Clinical Trials/NCT06311851

Transarterial Chemoembolization (TACE) Plus Bevacizumab for Liver Metastases

Is NCT06311851 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies Bevacizumab for cancer.

Phase 1/2RecruitingPardis Noor Medical Imaging and Cancer CenterNCT06311851Data as of Jun 2026Location: Iran

Treatment: BevacizumabTrans arterial chemoembolization (TACE) has emerged as a treatment option for chemotherapy-refractory diseases in Liver metastases. By delivering chemotherapy agents directly to the tumor site, TACE can maximize local drug concentrations and reduce systemic adverse reactions. Bevacizumab is a monoclonal antibody that functions as an angiogenesis inhibitor. It works by slowing the growth of new blood vessels by inhibiting vascular endothelial growth factor A (VEGF-A). The application of Bevacizumab during TACE has not been reported. In this study, we will evaluate the the overall survival (OS)、efficacy, and safety of the application of Bevacizumab during TACE in patients with Liver Metastases by designing an open, single-arm phase II clinical study.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Bevacizumab

Cancer type

Tumor Agnostic

Disease stage

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 80

Prior therapy

Cannot have received: liver resection

Prior liver resection

Cannot have received: transarterial chemoembolization

Previous TACE therapy received at other healthcare facilities

Lab requirements

Blood counts

platelet count >50×10^9 /L, hemoglobin >8.0 g/dL, ANC count ≥1.5 × 10^9/L

Kidney function

serum creatinine <1.5 times the upper limit of the normal range

Liver function

Child-Pugh class A or B; bilirubin <51 mmol/L; alanine and aspartate aminotransferase <3 times the upper limit of the normal range

Laboratory findings meeting specific criteria, including platelet count >50×10^9 /L, hemoglobin >8.0 g/dL, ANC count ≥1.5 × 10^9/L, bilirubin <51 mmol/L, alanine and aspartate aminotransferase <3 times the upper limit of the normal range, and serum creatinine <1.5 times the upper limit of the normal range.

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

Frequently asked questions

Is NCT06311851 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior liver resection, transarterial chemoembolization disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 80 years or younger.

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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