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Carcinoma clinical trials

View clinical trials related to Carcinoma.

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NCT ID: NCT01414426 Completed - Clinical trials for Precancerous Condition

Vandetanib in Preventing Head and Neck Cancer in Patients With Precancerous Head and Neck Lesions

Start date: January 2012
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well vandetanib works in preventing head and neck cancer in patients with precancerous head and neck lesions. Chemoprevention is the use of certain drugs to keep cancer from forming. The use of vandetanib may keep cancer from forming in patients with premalignant lesions

NCT ID: NCT01413113 Completed - Clinical trials for Recurrent Thyroid Cancer

Iodine I 131 and Pazopanib Hydrochloride in Treating Patients With Recurrent and/or Metastatic Thyroid Cancer Previously Treated With Iodine I 131 That Cannot Be Removed By Surgery

Start date: December 2011
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects and best dose of iodine I 131 when given together with pazopanib hydrochloride in treating patients with recurrent and/or metastatic thyroid cancer previously treated with iodine I 131 that cannot be removed by surgery. Radioactive drugs, such as iodine I 131, may carry radiation directly to cancer cells and not harm normal cells. Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving iodine I 131 together with pazopanib hydrochloride may be an effective treatment for thyroid cancer.

NCT ID: NCT01412671 Completed - Clinical trials for Carcinoma, Renal Cell

Nexavar Post-marketing Surveillance for RCC in Japan: Early Access Program

Start date: February 27, 2008
Phase:
Study type: Observational

This study is an early access program of 'Nexavar post-marketing surveillance (PMS) for renal cell carcinoma (RCC) in Japan' which is a regulatory, local prospective and observational study for patients with unresectable or advanced RCC under real-life practice conditions. The objective of this study is to assess safety and effectiveness of Nexavar at some limited sites which joined to clinical trial of Nexavar, before available of it in the market. The enrollment period is 2 months, and patients who received Nexavar will be recruited and followed one year since starting Nexavar administration. The data of this study will be integrated into the Nexavar PMS and the data will not be analyzed and reported alone.

NCT ID: NCT01411436 Completed - Clinical trials for Carcinoma, Hepatocellular

Nexavar Post-marketing Surveillance for Hepatocellular Carcinoma in Japan

Start date: May 2009
Phase: N/A
Study type: Observational

This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of patients who have received Nexavar for unresectable hepatocellular carcinoma (HCC). The objective of this study is to assess safety and effectiveness of Nexavar under real-life practice conditions. This study is an all case investigation of which the enrollment period is 2 or 3 months (dependent on sites) for Child-Pugh A; for Child-Pugh B or C, the enrollment continues until agreement to stop with Pharmaceuticals Medical Devices Agency (PMDA). All patients who have received Nexavar will be recruited and followed one year since starting Nexavar administration.

NCT ID: NCT01411423 Completed - Clinical trials for Carcinoma, Renal Cell

Nexavar Post-marketing Surveillance for Renal Cell Carcinoma in Japan

Start date: April 18, 2008
Phase:
Study type: Observational

This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of patients who have been administered with Nexavar for unresectable or advanced renal cell carcinoma (RCC). The objective of this study is to assess safety and effectiveness of Nexavar under real-life practice conditions. This study is an all case investigation of which the enrollment period is 15 months, and all patients who received Nexavar will be recruited and followed one year since starting Nexavar administration.

NCT ID: NCT01409499 Completed - Clinical trials for Hepatocellular Carcinoma

Palliative Treatments for Patients With Advanced Hepatocellular Carcinoma (HCC)

2011PTAHCC
Start date: January 2011
Phase: Phase 4
Study type: Interventional

The standard treatment choice for advanced hepatocellular carcinoma (HCC) is sorafenib, and its efficacy is limited. More active treatments were performed in patients with advanced HCC in China, which include radical hepatectomy or TACE. The study is to investigate whether the active treatment will profit survival of patients, and to evaluate the safety.

NCT ID: NCT01406574 Completed - Clinical trials for Hepatocellular Carcinoma

Phase I/II Study of OPB-31121 in Patients With Progressive Hepatocellular Carcinoma

Start date: July 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is: Phase1: To evaluate the safety and determine the recommended dose (RD) Phase2: To evaluate the efficacy

NCT ID: NCT01405183 Completed - Colorectal Cancer Clinical Trials

Association Between Hepatitis C Infection and Renal Cell Carcinoma

Start date: January 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine if there is an association between hepatitis C infection and kidney cancer. All patients who are diagnosed with kidney cancer and who will either have a biopsy or surgery will be offered to be tested for hepatitis C. The control group will be colon cancer patients. Both groups would be of recent diagnosis (6 months).

NCT ID: NCT01404104 Completed - Clinical trials for Renal Cell Carcinoma

Neo-adjuvant Temsirolimus in Patients With Advanced Renal Cell Carcinoma

Start date: September 2008
Phase: N/A
Study type: Interventional

Temsirolimus is a drug that is being studied to possibly treat kidney cancer. It works by starving the cancer of nutrients, by cutting off the blood supply, which is hoping to shrink the cancer. This study will look at the experimental use of temsirolimus, 12 weeks prior to the surgical removal of the entire kidney or a portion of the kidney that is involved by the tumor.

NCT ID: NCT01403480 Completed - Clinical trials for Basal Cell Carcinoma

Rates of Positive Basal Cell Carcinomas (BCCs) in Re-excisions

Start date: January 2008
Phase: N/A
Study type: Observational

Basal Cell Carcinoma (BCC) is the most common malignant growth in the world. Treatment is primarily surgical with the goal of excising the growth in its entirety. When pathology results show that this has not been achieved, a re-excision is routinely performed. This study examines retrospectively the percentage of re-excisions of BCC that actually proved to be positive (exhibited growth) among those re-excisions performed at Rambam Healthcare Campus and Zvulun Community Medical Center during the years 2008-10.