OncoMatch

OncoMatch/Clinical Trials/NCT03259867

Combination of TATE and PD-1 Inhibitor in Liver Cancer

Is NCT03259867 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Nivolumab Injectable Product and Trans-arterial tirapazamine embolization for hepatocellular carcinoma.

Phase 2RecruitingTeclison Ltd.NCT03259867Data as of Jun 2026

Treatment: Nivolumab Injectable Product · Trans-arterial tirapazamine embolizationThis is a multi-center, open-label phase IIA study that investigates the preliminary efficacy of Trans-arterial Tirapazamine Embolization (TATE) treatment of liver cancer followed by a PD-1 checkpoint inhibitor (nivolumab). Patients with two types of cancers will be enrolled, advanced hepatocellular carcinoma (HCC),and metastatic gastric cancer. All enrolled patients need to have liver lesions and have progressed on a prior immune checkpoint inhibitor.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Immunotherapy

Nivolumab Injectable Product

Other

Trans-arterial tirapazamine embolization

Cancer type

Hepatocellular Carcinoma

Gastric Cancer

Disease stage

Required: Stage IV

Metastatic disease required

advanced HCC or metastatic gastric cancer

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 80

Prior therapy

Must have received: immune therapy — advanced HCC

HCC patients...should have progressive disease (PD) on an immune therapy for advanced HCC

Must have received: systemic chemotherapy — metastatic gastric cancer

patients with metastatic gastric cancer...should have failed at least one line of systemic chemotherapy

Must have received: immune checkpoint inhibitor — metastatic gastric cancer

patients with metastatic gastric cancer...should have failed at least one line of...an immune checkpoint inhibitor

Lab requirements

Blood counts

Hgb >= 8, platelet >= 50,000

Kidney function

Cr <= 2

Liver function

AST and ALT < 10 X ULN, t-Bilirubin < 3, Child-Pugh scores 5-7 for HCC patients

Hgb>=8, platelet >= 50,000, Cr =< 2, AST and ALT < 10 X ULN, t-Bilirubin < 3, Child-Pugh scores 5-7 for HCC patients

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

US trial sites

  • University of California, Irvine · Orange, California
  • University of Oklahoma Health Science Center · Oklahoma City, Oklahoma
  • Medical College of Wisconsin · Milwaukee, Wisconsin

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT03259867 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received immune therapy and systemic chemotherapy.

What disease stage is eligible?

Stage IV is required (metastatic disease required).

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.

Check if I qualify