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Liver Cancer clinical trials

View clinical trials related to Liver Cancer.

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NCT ID: NCT01180959 Completed - Liver Cancer Clinical Trials

Erlotinib Plus Bevacizumab in Hepatocellular Carcinoma (HCC) as Second-line Therapy

Start date: April 14, 2011
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if the combination of AvastinTM (bevacizumab) and Tarceva (erlotinib hydrochloride) can help to control advanced liver cancer. The safety of this drug combination will also be studied.

NCT ID: NCT01178801 Recruiting - Liver Cancer Clinical Trials

Sharable Knowledge Mining Platform

Start date: March 2010
Phase: N/A
Study type: Observational

As a result of increasing adoption of health information systems in hospitals, more and more health records can be gathered and accumulated in the healthcare data repository. For this reason, the opportunity of analyzing and mining the healthcare data for quality improvement is increasing and becoming more and more important. The purpose of the project is to gather the clinical data relevant to liver cancer, and adopt the knowledge discovery and mining modules in information technology (IT) for analyzing and discovering the knowledge from the gathered clinical data. We can analyze the gathered clinical data for comparing the outcomes of different treatment strategies, finding out new diagnosis and staging criteria and factors, and other hidden knowledge included in the clinical data. Afterwards, the discovered results and the mining algorithms can be shared though the sharable knowledge mining platform provided by our project.

NCT ID: NCT01171924 Completed - Breast Cancer Clinical Trials

A Phase Ib Expansion Study Investigating the Safety, Efficacy, and Pharmacokinetics of Intravenous CUDC-101 in Subjects With Advanced Head and Neck, Gastric, Breast, Liver and Non-small Cell Lung Cancer Tumors

Start date: July 2010
Phase: Phase 1
Study type: Interventional

This is a phase Ib open label, expansion study of CUDC-101 in patients with advanced head and neck, gastric, breast, liver, and non-small cell lung cancer tumors. CUDC-101 is a multi-targeted agent designed to inhibit epidermal growth factor receptor (EGFR), human epidermal growth factor receptor Type 2 (Her2) and histone deacetylase (HDAC). The study is designed to compare the safety and tolerability of CUDC-101 when administered at the maximum tolerated dose on either a 5 days/week schedule or a 3 days/week schedule.

NCT ID: NCT01164202 Completed - Liver Cancer Clinical Trials

Chemoembolization of the Liver With or Without Sunitinib Malate in Treating Patients With Liver Cancer

SATURNE
Start date: July 2010
Phase: Phase 2/Phase 3
Study type: Interventional

RATIONALE: Chemoembolization kills tumor cells by blocking the blood flow to the tumor and keeping anticancer drugs near the tumor. Sunitinib malate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. It is not yet known whether chemoembolization is more effective with or without sunitinib malate in treating patients with liver cancer. PURPOSE: This randomized phase II/III trial is studying the side effects of chemoembolization of the liver and to see how well in works when given together with or without sunitinib malate in treating patients with liver cancer.

NCT ID: NCT01151761 Terminated - Liver Cancer Clinical Trials

PII of SBRT & Chemo for Unresectable Cholangiocarcinoma Followed by Liver Transplantation

Start date: January 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine progression-free survival at 12 months for stereotactic body radiotherapy (SBRT) and chemotherapy for unresectable hilar cholangiocarcinoma (CCA). Investigators hope to learn more about neoadjuvant SBRT and chemotherapy for unresectable CCA, and if SBRT followed by chemotherapy can lead to successful liver transplantation. This knowledge is important for this patient group as this disease is a highly lethal malignancy that often presents as unresectable, however surgery or transplantation are the only curative options.

NCT ID: NCT01099631 Completed - Liver Cancer Clinical Trials

IL-2 Expressing, Attenuated Salmonella Typhimurium in Unresectable Hepatic Spread

Start date: April 2010
Phase: Phase 1
Study type: Interventional

The working hypothesis is that oral administration of an attenuated strain of Salmonella typhimurium is safe and efficacious for patients with unresectable hepatic metastasis from a solid tumor cancer. The primary objective of the study is to determine the MTD of Salmonella typhimurium in the treatment.

NCT ID: NCT01082224 Active, not recruiting - Liver Cancer Clinical Trials

Contrast-Enhanced CT and MRI in Diagnosing and Staging Liver Cancer Using UNOS Policy

ACRIN6690
Start date: December 2010
Phase: N/A
Study type: Interventional

RATIONALE: Diagnostic procedures, such as contrast-enhanced CT scan and contrast-enhanced MRI, may help find liver cancer and find out how far the disease has spread. PURPOSE: This clinical trial is studying contrast-enhanced CT scan and contrast-enhanced MRI in diagnosing and staging liver cancer in patients with chronic liver disease.

NCT ID: NCT01079767 Terminated - Liver Cancer Clinical Trials

Temsirolimus in Treating Patients With Advanced Liver Cancer and Cirrhosis

Start date: January 2010
Phase: Phase 2
Study type: Interventional

RATIONALE: Temsirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase II trial is studying how well temsirolimus works in treating patients with advanced liver cancer and cirrhosis.

NCT ID: NCT01076517 Approved for marketing - Liver Cancer Clinical Trials

A Humanitarian Device Exemption Treatment Protocol of TheraSphere For Treatment of Unresectable Hepatocellular Carcinoma

Start date: n/a
Phase:
Study type: Expanded Access

To provide Therasphere treatment for patients diagnosed with unresectable liver cancer.

NCT ID: NCT01075555 Completed - Liver Cancer Clinical Trials

Sorafenib Tosylate With or Without Pravastatin in Treating Patients With Liver Cancer and Cirrhosis

Start date: February 2010
Phase: Phase 3
Study type: Interventional

RATIONALE: Sorafenib tosylate and pravastatin may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Sorafenib tosylate may also stop the growth of liver cancer by blocking blood flow to the tumor. It is not yet known whether sorafenib tosylate is more effective when given alone or together with pravastatin in treating patients with liver cancer and cirrhosis. PURPOSE: This randomized phase III trial is studying sorafenib tosylate given together with pravastatin to see how well it works compared with giving sorafenib tosylate alone in treating patients with liver cancer and cirrhosis.