Combination of TATE and PD-1 Inhibitor in Liver Cancer

Recruiting Phase 2 Interventional Study
Hepatocellular Carcinoma Gastric Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 80
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
54 (estimated)
Sponsor
Teclison Ltd. · Industry
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About This Trial
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…
Trial Locations
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Eligibility Criteria
1. Patients with a confirmed diagnosis of (1) advanced HCC or (2) metastatic gastric cancer. 2. Patients between ages 18 and 80 3. If HCC patients, they should have progressive disease (PD) on an immune therapy for advanced HCC. For patients with metastatic gastric cancer, they should have failed at…
Contacts

Ray Lee, MD. PhD

8043341076

ray.lee01@teclison.com

CONTACT

Chiwei Lu, PhD.

chiwei.lu4@teclison.com

CONTACT