Last updated on June 2017

First-in-Human Safety and Tolerability Study of MTL-CEBPA in Patients With Advanced Liver Cancer


Brief description of study

This is a First in Human study of a new single agent (MTL-CEBPA) in patients with advanced cancer of the liver. The study is in two parts: dose escalation followed by a dose expansion; both parts of the study will recruit advanced hepatocellular carcinoma patients with cirrhosis. All participants will be refractory to or ineligible for loco-regional therapy including surgery, radiofrequency tumour ablation, transarterial chemoembolisation or sorafenib. MTL-CEBPA consists of a double stranded RNA formulated into a SMARTICLES® liposomal nanoparticle and is designed to activate the CEBPA gene.

Clinical Study Identifier: NCT02716012

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Dr Han Chong Toh

National Cancer Centre
Singapore, Singapore
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Dr Cheng Ean Chee

National University Hospital
Singapore, Singapore
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Professor Kai-Wen Huang

National Taiwan University Hospital
Taipei, Taiwan
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Dr yuk-Ting Ma

University Hospitals Birmingham NHS Foundation Trust
Birmingham, United Kingdom
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Dr Bristi Basu

Cambridge University Hospitals NHS Trust
Cambridge, United Kingdom
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Professor Jeff Evans

The Beatson West of Scotland Cancer Centre
Glasgow, United Kingdom
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Professor Daniel Palmer

Clatterbridge Cancer Centre NHS Foundation Trust
Liverpool, United Kingdom
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Dr Debashis Sarker

Guy's and St. Thomas' NHS Foundation Trust
London, United Kingdom
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Professor Long R Jiao

Imperial College Healthcare NHS Trust
London, United Kingdom
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Professor Tim Meyer

University College London Hospitals NHS Foundation Trust
London, United Kingdom
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Professor Ruth Plummer

Newcastle upon Tyne Hospitals NHS Foundation Trust
Newcastle, United Kingdom
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