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Carcinoma clinical trials

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NCT ID: NCT00357422 Completed - Clinical trials for Hepatocellular Carcinoma

Comparison Study of Operation and PEIT for Small, Solitary Hepatocellular Carcinoma (HCC)

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to choose the preferred treatment modality for solitary, small hepatocellular carcinoma.

NCT ID: NCT00356460 Completed - Melanoma Clinical Trials

Safety and Efficacy Study of GC1008 to Treat Renal Cell Carcinoma or Malignant Melanoma

Start date: September 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, pharmacokinetics and pharmacodynamics of GC1008, a human anti-transforming growth factor-beta (TGFβ) monoclonal antibody in previously treated patients with locally advanced or metastatic renal cell carcinoma or malignant melanoma.

NCT ID: NCT00355862 Completed - Clinical trials for Hepatocellular Carcinoma

Immunosuppression in Patients Undergoing Liver Transplantation for Hepatocellular Carcinoma

Start date: January 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of sirolimus-based immunosuppressive therapy in patients following orthotopic liver transplantation (OLT) for hepatocellular carcinoma (HCC), with regard to HCC recurrence-free patient survival.

NCT ID: NCT00355355 Completed - Clinical trials for Carcinoma, Hepatocellular

A Phase 3 Study of Talaporfin Sodium and Interstitial Light Emitting Diodes Treating Hepatocellular Carcinoma (HCC)

Start date: July 2006
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the survival of patients treated with Litx™ versus standard of care therapies in the treatment of unresectable hepatocellular carcinoma (HCC), and to demonstrate the safety of Litx™ therapy. Litx™ consists of a light-activated drug, talaporfin sodium (LS11, Light Sciences Oncology, Bellevue, Washington), and a light generating device, composed of light-emitting diodes (LEDs), that is energized by a power controller and percutaneously placed in the target tissue inside the body.

NCT ID: NCT00355238 Completed - Clinical trials for Hepatocellular Carcinoma (HCC)

A Phase II Open Label Study of BMS-582664 in Locally Advanced or Metastatic Hepatocellular Cancer

Start date: December 31, 2006
Phase: Phase 2
Study type: Interventional

The purpose of this clinical research study is to learn if BMS-582664 can shrink or slow the growth of advanced liver cancer. The safety of this treatment will also be studied.

NCT ID: NCT00353301 Completed - Clinical trials for Renal Cell Carcinoma

Erlotinib and Sirolimus for the Treatment of Metastatic Renal Cell Carcinoma

Start date: July 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test the safety and efficacy of the combination of erlotinib hydrochloride (Tarceva™) and sirolimus (Rapamune™) in the treatment of patients with metastatic kidney cancer.

NCT ID: NCT00353015 Completed - Clinical trials for Gastrointestinal Cancer

Irinotecan and Cisplatin for High Grade Neuroendocrine Carcinoma of the Gastrointestinal Tract

Start date: March 2003
Phase: Phase 2
Study type: Interventional

Primary Objective: 1. Assess the clinical activity defined by response rate of irinotecan and cisplatin in untreated patients with metastatic or unresectable high grade neuroendocrine carcinoma of the gastrointestinal tract. Secondary Objective: 1. To assess the safety profile of irinotecan and cisplatin in untreated patients with metastatic or unresectable high grade neuroendocrine carcinoma of the gastrointestinal tract.

NCT ID: NCT00352300 Completed - Neutropenia Clinical Trials

Carboplatin, Paclitaxel, and Pegfilgrastim in Treating Patients With Stage III or Stage IV Ovarian Epithelial, Fallopian Tube, Primary Peritoneal, or Carcinosarcoma Cancer

Start date: June 2006
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects of giving carboplatin and paclitaxel together with pegfilgrastim in treating patients with stage III or stage IV ovarian epithelial, fallopian tube, primary peritoneal, or carcinosarcoma cancer. Drugs used in chemotherapy, such as carboplatin and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Colony-stimulating factors, such as pegfilgrastim, may increase the number of immune cells found in bone marrow or peripheral blood and may help the immune system recover from the side effects of chemotherapy. Giving carboplatin and paclitaxel together with pegfilgrastim after surgery may kill any tumor cells that remain after surgery.

NCT ID: NCT00351949 Completed - Clinical trials for Stage IV Renal Cell Carcinoma

IMP321 Phase 1 Trial in Metastatic Renal Cell Carcinoma (MRCC)

Start date: September 2005
Phase: Phase 1
Study type: Interventional

Single-center, open label, non-randomized, fixed dose-escalation, phase 1 study, performed in ambulatory and day-hospital setting

NCT ID: NCT00341146 Completed - Clinical trials for Nasopharyngeal Carcinoma

Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s)

Start date: April 1, 2001
Phase:
Study type: Observational

The objective of this study is to characterize genes associated either with susceptibility or resistance to the development nasopharyngeal carcinoma (NPC) in a Chinese population where the incidence of NPC is as high as 50 in 100,000. NPC has been and remains a unique model of human malignancy for understanding a multi-step carcinogenic process involving a ubiquitous virus (Epstein-Barr virus), environmental carcinogens, and an NPC susceptibility gene. Up to 95% of all NPC patients at early or late stage of the disease have IgA antibodies directed to the EBV virus VCA (viral capsid antigen). Environmental factors have also been implicated as significant risk factors in the development of NPC. In addition, certain alleles in HLA genes have shown associations with NPC, perhaps in concert with a family of T-cell receptor genes (TCR). Other data suggest that a microsatellite marker on Chromosome 6 may be associated with an NPC-disease associated gene.