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Carcinoma, Hepatocellular clinical trials

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NCT ID: NCT03695952 Recruiting - Clinical trials for Hepatocellular Carcinoma

A Prospective Cohort Study of Patients With Hepatobiliary Cancer Treated With Immune Checkpoint Inhibitors

Start date: July 1, 2018
Phase:
Study type: Observational [Patient Registry]

Although immune checkpoint inhibitors including nivolumab and pembrolizumab are now available for the management of hepatobiliary cancers in Korea, there is a lack of data for the efficacy and safety of these agents in the real-world setting. This study aims to prospectively evaluate the efficacy of safety of nivolumab and pembrolizumab against advanced hepatocellular carcinoma and biliary tract cancer.

NCT ID: NCT03695250 Terminated - Clinical trials for Unresectable Hepatocellular Carcinoma

BMS-986205 and Nivolumab as First or Second Line Therapy in Treating Patients With Liver Cancer

Start date: October 16, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial studies the side effects and best dose of IDO1 inhibitor BMS-986205 (BMS-986205) when given together with nivolumab and how well it works as first or second line therapy in treating patients with liver cancer. BMS-986205 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as nivolumab, may interfere with the ability of tumor cells to grow and spread. Giving BMS-986205 and nivolumab may work better in treating patients with liver cancer.

NCT ID: NCT03686709 Recruiting - Clinical trials for Hepatocellular Carcinoma

Y90 Radioembolization Dose Delivery and Radiation Exposure Assessment

Start date: June 19, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to examine critical aspects of radiation exposure, dose delivery, and systemic yttrium-90 (Y90) exposure related to the infusion of Y90 microspheres for treatment of hepatocellular carcinoma (HCC) and other metastatic liver disease.

NCT ID: NCT03682276 Recruiting - Clinical trials for Hepatocellular Carcinoma

Safety and Bioactivity of Ipilimumab and Nivolumab Combination Prior to Liver Resection in Hepatocellular Carcinoma

PRIME-HCC
Start date: March 1, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The PRIME-HCC trial will assess the effects of combination treatment with nivolumab (OPDIVO) and ipilimumab (YERVOY) pre-operatively in hepatocellular carcinoma patients for whom liver resection is planned. The trial will be conducted at a small number of National Health Service hospitals in the UK. Participants will receive two doses of nivolumab and a single dose of ipilimumab in the weeks before their planned surgery.

NCT ID: NCT03674073 Recruiting - Clinical trials for Hepatocellular Carcinoma

A Study Combining Personalized Neoantigen-based Dendritic Cell Vaccine With Microwave Ablation for the Treatment of Hepatocellular Carcinoma

Start date: October 15, 2018
Phase: Phase 1
Study type: Interventional

This is a single institution, open-label, multi-arm, pilot study of a personalized neoantigen-based dendritic cell (DC) vaccine combined with microwave ablation in subjects with Hepatocellular Carcinoma (HCC). Patients with HKLC stage IIa HCC are eligible for enrollment. In this study, the investigators are looking at the safety, feasibility of the personalized neoantigen-based DC vaccine combined with microwave ablation as well as the T cell immune response to the vaccine.

NCT ID: NCT03672305 Not yet recruiting - Clinical trials for Primary Hepatocellular Carcinoma

Clinical Study on the Efficacy and Safety of c-Met/PD-L1 CAR-T Cell Injection in the Treatment of HCC

Start date: October 1, 2018
Phase: Early Phase 1
Study type: Interventional

Title: Single-center, open clinical study on the efficacy and safety of c-Met/PD-L1 T cell injection in the treatment of primary hepatocellular carcinoma Stage: Phase I clinical trial Purpose: To evaluate the efficacy and safety of c-Met/PD-L1 CAR-T cells in patients with primary hepatocellular carcinoma Object: patients with primary hepatocellular carcinoma Sample size: 50 cases Number of centres:1 Study design: CT, MRI, PET and blood biochemical tests were performed before treatment to evaluate the state of HCC. Peripheral blood of the patient was extracted and PBMC was isolated. CAR-T cells were obtained by tranducing PBMC with c-Met/PD-L1 CAR lentivirus, and the proliferation capacity and immune phenotype of the cells were tested. After passing the inspection, the cells were re-injected into the patient three times. The efficacy and safety of c-Met/PD-L1 CAR-T cells was assessed respectively at 4 week, 12 week, 24 week and 48 week after treatment. Trial product: c-Met/PD-L1 CAR-T cells Course of treatment: 3 days for a course of treatment, only one course of treatment. A second course is given as appropriate if the treatment is beneficial to the patient.

NCT ID: NCT03668158 Not yet recruiting - Clinical trials for Hepatocellular Carcinoma

Multi-center Study on Therapy-oriented Molecular Subtyping of Hepatocellular Carcinoma

Start date: November 20, 2018
Phase:
Study type: Observational

The purpose of this study is to establish molecular subtyping of HCC.

NCT ID: NCT03663114 Completed - Clinical trials for Carcinoma, Hepatocellular

A Post-marketing Observational Study on Risk Factors for Hepatic Encephalopathy in Participants With Unresectable Hepatocellular Carcinoma

Start date: July 2, 2018
Phase:
Study type: Observational

This study is a post-marketing observational study of lenvatinib in participants with unresectable hepatocellular carcinoma. The primary objective of this study is assessment of risk factors for hepatic encephalopathy.

NCT ID: NCT03662841 Terminated - Clinical trials for Carcinoma, Hepatocellular

Ablative Chemoembolization for Unresectable and Large Hepatocellular Carcinoma

Start date: July 13, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to study the safety and tumor response of ACE for large HCC.

NCT ID: NCT03655002 Active, not recruiting - Clinical trials for Recurrent Hepatocellular Carcinoma

IRX-2, Cyclophosphamide, and Nivolumab in Treating Patients With Recurrent or Metastatic and Refractory Liver Cancer

Start date: February 21, 2019
Phase: Phase 1
Study type: Interventional

This phase Ib trial studies the side effects and best dose of IRX-2 when given together with cyclophosphamide and nivolumab in treating patients with liver cancer that has come back or spread to other parts of the body and does not response to treatment. Biological therapies, such as IRX-2, may stimulate or suppress the immune system in different ways and stop tumor cells from growing. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving IRX-2, cyclophosphamide, and nivolumab may work better than the IRX?2 regimen alone in treating patients with hepatocellular carcinoma.