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NCT03259867 · ClinicalTrials.gov registry record · Phase 2

Combination of TATE and PD-1 Inhibitor in Liver Cancer

A Phase 2 study of Gastric Cancer and Hepatocellular Carcinoma, sponsored by Teclison.

Recruiting
Registry status
Phase 2
Development phase
54
Enrollment target
3
Study locations

NCT03259867 is a Phase 2 study of Gastric Cancer and Hepatocellular Carcinoma that is actively recruiting participants, run by Teclison. The registered enrollment target is 54 participants, below the 319-participant average among 153 other Gastric Cancer trials with a reported enrollment target (83% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT03259867, a Phase 2 study of Gastric Cancer and Hepatocellular Carcinoma, is actively recruiting participants, sponsored by Teclison.

RECRUITING
Registry status
Phase 2
Development phase
54 participants
Enrollment target
3
Study locations

Study Summary

This 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.

Interventions

  • DRUG Nivolumab Injectable Product
  • COMBINATION_PRODUCT Trans-arterial tirapazamine embolization

Study Locations (3)

California

  • University of California, Irvine - Orange

Oklahoma

  • University of Oklahoma Health Science Center - Oklahoma City

Wisconsin

  • Medical College of Wisconsin - Milwaukee

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2017-07-01
Est. Completion 2025-12-31
Phase Phase 2

Sponsor

Teclison

4 total trials

What the Registry Record Tells You About NCT03259867

The ClinicalTrials.gov registry entry for NCT03259867 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 319-participant average among 153 other Gastric Cancer trials with a reported enrollment target (83% lower). The listed sponsor is Teclison, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Gastric Cancer appearing as the primary indexed condition, and to 2 interventions - of which Nivolumab Injectable Product is the first listed.

NCT03259867 reports 3 study locations spanning 3 distinct geographic areas - top geographies include California, Oklahoma, Wisconsin.

Frequently Asked Questions

What is clinical trial NCT03259867 about?

NCT03259867 is a clinical study titled "Combination of TATE and PD-1 Inhibitor in Liver Cancer". This 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...

What is the current status of trial NCT03259867?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 54 participants. The study started on 2017-07-01. Estimated completion is 2025-12-31.

What conditions does trial NCT03259867 study?

This clinical trial studies the following conditions: Gastric Cancer, Hepatocellular Carcinoma.

What interventions are being tested in trial NCT03259867?

The interventions under investigation include: Nivolumab Injectable Product (DRUG), Trans-arterial tirapazamine embolization (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT03259867?

This trial is sponsored by Teclison, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03259867 being conducted?

This trial has 3 study locations across California, Oklahoma, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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