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Study details
Enrolling now

Combination of TATE and PD-1 Inhibitor in Liver Cancer

Teclison Ltd.
NCT IDNCT03259867ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

54

Study length

about 8.5 years

Ages

18–80

Locations

3 sites in CA, OK, WI

What this study is about

Researchers are testing the effectiveness of Trans-arterial Tirapazamine Embolization (TATE) treatment for liver cancer, followed by a PD-1 checkpoint inhibitor (nivolumab). The trial will enroll adults with advanced hepatocellular carcinoma (HCC) and metastatic gastric cancer who have progressed on a prior immune checkpoint inhibitor.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive Nivolumab Injectable Product
  • 2.Take Trans-arterial tirapazamine embolization

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVInjection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

immunotherapy (Immune checkpoint inhibitor; blocks PD-1 receptor on T cells)

Drug routes

infusion, injection

Endpoints

Primary: Overall Response Rate

Secondary: Duration of Response, Overall survival, Progression Free Survival, Time to Progression