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Hepatocellular Carcinoma clinical trials

View clinical trials related to Hepatocellular Carcinoma.

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NCT ID: NCT03259581 Completed - Clinical trials for Hepatocellular Carcinoma

Safety of Transarterial Chemoembolization (TACE) in the Setting of an Elevated Bilirubin

Start date: January 2, 2018
Phase: Phase 1
Study type: Interventional

The aim of this study is to evaluate the safety of selective transarterial chemoembolization (TACE) of hepatocellular carcinoma (HCC) in the setting of an elevated total bilirubin, but relatively normal direct bilirubin.

NCT ID: NCT03254121 Completed - Clinical trials for Hepatocellular Carcinoma

Genome Studies of Hepatocellular Carcinoma Developed in Hepatitis C Patients With Sustained Virological Response

HEPCASUS
Start date: January 1, 2017
Phase:
Study type: Observational

In this international collaboration study, the research group will analyze somatic mutations of hepatocellular carcinoma (HCC) developed after sustained virological response (SVR) in patients treated with hepatitis C (HCV) therapy

NCT ID: NCT03248375 Completed - Clinical trials for Hepatocellular Carcinoma

Impact of Y90 Radiation Segmentectomy on HCC

Start date: August 3, 2016
Phase: N/A
Study type: Interventional

The aim of this pilot study is to assess the efficacy of radiation segmentectomy with Theraspheres in patients with unresectable hepatocellular carcinoma that would qualify for thermal ablation as per the BCLC guidelines, but are unable to receive thermal ablation due to unfavorable location of target lesions.

NCT ID: NCT03245190 Completed - Clinical trials for Hepatocellular Carcinoma

Study of Chiauranib in Patients With Advanced Hepatocellular Carcinoma

Start date: April 28, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Chiauranib, which simultaneously targets against VEGFR/Aurora B/CSF-1R, several key kinases involved in tumor angiogenesis, tumor cell mitosis, and chronic inflammatory microenvironment.

NCT ID: NCT03233360 Completed - Clinical trials for Hepatocellular Carcinoma

Hepatocellular Carcinoma Registry in Asia: The INSIGHT Registry

INSIGHT
Start date: April 17, 2017
Phase:
Study type: Observational

The INSIGHT ('Insight into Real-world Practice of Management of HCC in Asia-Pacific') registry is designed as a multi-centre longitudinal cohort study of patients diagnosed with HCC between 1st January 2013 and 31st December 2019 in nine countries (i.e., South Korea, Taiwan, Thailand, Japan, China, Hong Kong, Australia, New Zealand and Singapore). Approximately 30% of the sample size will be identified retrospectively and 70% will be identified prospectively from the start date of the registry (October 2016), with an even distribution of consecutively diagnosed patients within the different years.

NCT ID: NCT03232593 Completed - Clinical trials for Hepatocellular Carcinoma

A Study of Atezolizumab (Tecentriq®) in Ministry of Food and Drug Safety (MFDS)-Approved Indication(s)

Start date: November 29, 2017
Phase:
Study type: Observational

This Phase 4, prospective, multicenter, non-interventional, regulatory post-marketing surveillance study will collect information on the the safety and effectiveness of atezolizumab under the clinical practice, and update the drug label approved by the MFDS in Korea.

NCT ID: NCT03222076 Completed - Clinical trials for Hepatocellular Carcinoma

Nivolumab With or Without Ipilimumab in Treating Patients With Resectable Liver Cancer

Start date: September 28, 2017
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side effects and how well nivolumab with or with ipilimumab works in treating patients with liver cancer that can be removed by surgery. Immunotherapy with monoclonal antibodies, such as nivolumab and ipilimumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.

NCT ID: NCT03212625 Completed - Clinical trials for Hepatocellular Carcinoma

The Effect of Urea Cream on Sorafenib-associated Hand-Foot Skin Reaction

Start date: January 28, 2016
Phase: Phase 4
Study type: Interventional

Many investigators have studied for prevention and care of Hand-Foot Skin Reaction(HFSR), and urea cream is typical representative. Recent study was performed prevention effect of urea cream for Hand-Foot Skin Reaction(HFSR) on 871 Chinese. But the study did not designed as placebo-control group and it had big defect in double-blinded. Therefore, it needs complementary study as double-blinded placebo-controlled trial and effect of urea cream on Korean patient group.

NCT ID: NCT03203005 Completed - Clinical trials for Hepatocellular Carcinoma

IMA970A Plus CV8102 in Very Early, Early and Intermediate Stage Hepatocellular Carcinoma Patients

Start date: September 18, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This study is being carried out in order to evaluate a new cancer vaccine called IMA970A combined with CV8102, a new adjuvant for the treatment of liver cancer (hepatocellular carcinoma). It will be investigated whether IMA970A and CV8102 is safe and can trigger an immune response against the tumor, which may prevent the tumor (cancer) from recurring or spreading or may even lead to tumor shrinkage following the standard treatments the patients have previously received.

NCT ID: NCT03197155 Completed - Clinical trials for Hepatocellular Carcinoma

Direct-acting Antivirals and Hepatocellular Carcinoma Recurrence

RECAR
Start date: June 1, 2016
Phase: N/A
Study type: Observational

Background and Aims: Arrival of direct-acting antiviral (DAA) agents against hepatitis C virus (HCV) with high-sustained virological response (SVR) rates and very few side effects has drastically changed the management of HCV infection. The impact of DAA exposure on hepatocellular carcinoma (HCC) recurrence after a first remission in patients with advanced fibrosis remains to be clarified. Methods: 68 consecutive HCV patients with a first HCC diagnosis and under remission, subsequently treated or not with a DAA combination, were included. Clinical, biological, and virological data were collected at first HCC diagnosis, at remission and during the surveillance period.