A Phase I/Ib trial of Ad-REIC in liver cancer: study protocol

Author:

Oyama Astushi1ORCID,Shiraha Hidenori1,Uchida Daisuke1,Iwamuro Masaya2,Kato Hironari1,Takaki Akinobu1,Ikeda Fusao1,Onishi Hideki1,Yasunaka Tetsuya1,Takeuchi Yasuto1,Wada Nozomu1,Iwasaki Yoshiaki1,Sakata Masahiro1,Okada Hiroyuki1,Kumon Hiromi3

Affiliation:

1. Department of Gastroenterology & Hepatology, Okayama University Faculty of Medicine, 2-5-1, Shikata-cho, Okayama 700-8558, Japan

2. Department of General Medicine, Okayama University Faculty of Medicine, 2-5-1, Shikata-cho, Okayama 700-8558, Japan

3. Innovation Center Okayama for Nanobio-Targeted Therapy (ICONT), Okayama University, 2-5-1, Shikata-cho, Okayama 700-8558, Japan

Abstract

This study will assess the safety and efficacy of the administration of adenoviral vector expressing the human-reduced expression in immortalized cells (Ad-REIC) to a liver tumor in patients with hepatocellular carcinoma (HCC) or liver metastasis of pancreatic cancer. A Phase I clinical study of Ad-REIC administration to a liver tumor in a patient with HCC or liver metastasis of pancreatic cancer will be conducted. The study is a single-arm, prospective, nonrandomized, noncomparative, open-label, single-center trial performed in Okayama University Hospital, Okayama, Japan. Ad-REIC will be injected into the liver tumor under ultrasound guidance. Ad-REIC administration will be repeated a total of three-times every 2 weeks. The primary end point is the dose-limiting toxicity and incidence of adverse events. The secondary end points are the objective response rate and disease control rate. This study aims to expand the indication of Ad-REIC by assessing its safety and efficacy in patients with HCC or liver metastasis of pancreatic cancer.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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