Clinical Trials Logo

Carcinoma, Hepatocellular clinical trials

View clinical trials related to Carcinoma, Hepatocellular.

Filter by:

NCT ID: NCT03230318 Completed - Clinical trials for Intrahepatic Cholangiocarcinoma

Derazantinib in Subjects With FGFR2 Gene Fusion-, Mutation- or Amplification- Positive Inoperable or Advanced Intrahepatic Cholangiocarcinoma

FIDES-01
Start date: September 28, 2017
Phase: Phase 2
Study type: Interventional

This Phase II, open-label, single-arm study evaluated the anti-cancer activity of derazantinib in subjects with inoperable or advanced intrahepatic cholangiocarcinoma (iCCA) who received at least one prior regimen of systemic therapy. Patients received an oral once-daily total dose of 300 mg derazantinib capsules.

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: NCT03215290 Completed - Clinical trials for Liver Carcinoma Resectable

Trans-parenchymal Compressing Suture in Major Liver Resection

Start date: October 2016
Phase: N/A
Study type: Interventional

Non-anatomical liver resection with appropriate resection margin was regarded as a potential curative treatment for selected major hepatic carcinoma due to preserving maximal normal liver, especially in cirrhotic patients. But occurrence of cutting surface related complications become a main challenge.

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: NCT03200171 Completed - Hepatitis C Clinical Trials

Effect of DAAs on Behavior of HCC in HCV Patients

Start date: February 10, 2018
Phase:
Study type: Observational

Investigators aim to study the effect of direct acting antiviral agents (DAAs) on behavior of hepatocellular carcinoma (HCC) and overall survival in patients with chronic hepatitis C (CHC).

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.

NCT ID: NCT03178409 Completed - Clinical trials for Hepatocellular Carcinoma

Combined HCC-MFCCC

Start date: January 1, 2004
Phase: N/A
Study type: Observational

Combined hepatocellular and mass-forming cholangiocarcinoma (cHCC-MFCCC) is a rare tumor. The aim of this study was the analysis of the outcome comparing such tumor with classic hepatocellular carcinoma (HCC) and mass-forming cholangiocarcinoma (MFCCC).

NCT ID: NCT03176485 Completed - Clinical trials for Hepatocellular Carcinoma

Evaluation of Pathway Modulation by Raf, MEK, & Kinase Inhibitors

Start date: October 17, 2014
Phase: N/A
Study type: Interventional

This is a pilot study designed to evaluate the cutaneous effect of systemic inhibition of the tyrosine kinase pathway in the presence or absence of solar simulated light exposure. A maximum of 45 subjects will be accrued into the overall study we anticipate approximately 25 patients in the Raf inhibitor group and 10 patients each into the Tyrosine Kinase and MEK inhibitor arms of the study.

NCT ID: NCT03164382 Completed - Liver Cancer Clinical Trials

Hepatic Arterial Infusion of Oxaliplatin, Fluorouracil/Leucovorin Versus Sorafenib in Advanced Hepatocellular Carcinoma

Start date: March 1, 2017
Phase: Phase 3
Study type: Interventional

This trial was designed to investigate whether the survival outcome, response rate and safety of hepatic arterial infusion of oxaliplatin, fluorouracil/leucovorin regimens for patients with Barcelona-Clinic Liver Cancer (BCLC)-C stage hepatocellular carcinoma was superior than those of the standard treatment with sorafenib or not.