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Neoplasms clinical trials

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NCT ID: NCT00436423 Completed - Neoplasm Metastasis Clinical Trials

A Phase Ⅱ Study of Gemcitabine Combination With TS-1 in Patient With Advanced or Recurred Pancreatic Cancer

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

The primary objective of the study is to Evaluate the response rate of Gemcitabine with TS-1 in Korean patient with advanced but inoperable, metastatic or recurrent pancreatic cancer who is not receiving anti cancer therapy.

NCT ID: NCT00435214 Completed - Cervical Neoplasia Clinical Trials

Human Papillomavirus (HPV) and Risk of Cervical Precancer and Cancer

Start date: January 29, 2007
Phase:
Study type: Observational

Background: - In most women, HPV infection does not cause symptoms and the infection goes away on its own. In a small percentage of women, the HPV infection does not go away and sometimes can result in cervical precancer or cancer. - There are several different types of HPV. A better understanding of which types are related to cervical precancer and cancer may help guide doctors in clinical management of women who test positive for HPV and better understand why some women develop disease while others do not. Objectives: - To determine whether certain types of HPV are more risky than others and if so, whether they warrant separate detection in screening for cervical precancer and cancer. - To determine if lasting infection by different HPV types carry different risk of cervical precancer and cancer. - To determine what viral and genetic factors influence the development of cervical precancer and cancer. - To evaluate new HPV tests and new biomarkers of cervical cancer risk. Eligibility: -Women 30 years of age and older who are in the cervical cancer screening program at the Kaiser Permanente health plan in Northern California. Women who tested positive for HPV and a random sample of women who tested negative for the virus are included. Design: -Data about participants genetic background and the type of carcinogenic HPV with which they are infected are analyzed.

NCT ID: NCT00434109 Completed - Clinical trials for Neuroendocrine Tumor

Phase II Study of Sunitinib Malate Following Hepatic Artery Embolization

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

The purpose of this study is to decide if a medicine that slows growth of new blood vessels can be give after the embolization procedure to prevent or delay new growth of blood vessels to tumors.

NCT ID: NCT00433485 Completed - Clinical trials for Non-melanomatous Skin Cancer

Topical Sirolimus in Patients With Basal Cell Nevus Syndrome and in Healthy Participants

Start date: n/a
Phase: Phase 1
Study type: Interventional

RATIONALE: Studying samples of blood and tissue from patients with basal cell nevus syndrome and from healthy participants in the laboratory may help doctors learn more about changes that may occur in DNA and identify biomarkers related to basal cell nevus syndrome. Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. The use of sirolimus may keep basal cell skin cancer from forming in patients with basal cell nevus syndrome. PURPOSE: This phase I trial is studying topical sirolimus in patients with basal cell nevus syndrome and in healthy participants.

NCT ID: NCT00432302 Completed - Neoplasms Clinical Trials

Investigation of Mass Balance of the Test Drug and Major Metabolites

Start date: January 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to: a) Determine how the body takes up the test drug and distributes it into various body organs and tissues, how it processes the drug and how it ultimately removes it; and b) Examine how well the test drug works against cancer, and whether it is safe and tolerable to take

NCT ID: NCT00429416 Completed - Clinical trials for Hematologic Malignancies

Research Study to Determine if an Experimental Agent, LLME Can Decrease the Incidence and Severity of Graft-Versus-Host-Disease (GVHD) Following Blood (Hematopoietic) Stem Cell Transplantation

Start date: March 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research study is to determine if an experimental agent, LLME can decrease the incidence and severity of Graft-Versus-Host-Disease (GVHD) following blood (hematopoietic) stem cell transplantation

NCT ID: NCT00429143 Completed - Clinical trials for Hematologic Malignancies

A Two-Step Approach to Bone Marrow Transplant Using Cells From A Partially-Matched Relative

Start date: January 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to develop a way of treating patients who do not have a completely matched family donor or a readily available unrelated donor with bone marrow transplant by using a partially-matched family donor. Patients receiving this type of transplant will receive chemotherapy and/or radiation to treat their disease. They will also receive their donor's cells in 2 parts. During the first part, the donor's lymphocytes will be exposed to one of the chemotherapy agents to help the patient become tolerant to the lymphocytes. In the second part of the transplant, the patient will receive their donor's stem cells to help recover their peripheral blood counts and establish long-term engraftment. The hypothesis of this study is that in partially-matched allogeneic transplant, there is a defined number of donor T-cells that can be treated and given to the recipient to avoid post-transplant infection without causing severe graft-versus-host disease.

NCT ID: NCT00428675 Completed - Neoplasms Clinical Trials

A New Tool for Assessing Fatigue in Individuals With Advanced Cancer

Start date: October 2005
Phase:
Study type: Observational

Fatigue is a common problem in advanced cancer and palliative care. The development of tools to measure fatigue, however, has been slowed by their inability to distinguish between fatigue and other related symptoms, such as tiredness. Our work suggests that these distinctions are important because they serve as markers for stressors associated with advancing disease. We have developed a tool that we believe will distinguish between these two states as well as exhaustion. In this study we will conduct some initial tests of this tool in preparation for its use as an outcome indicator in future studies.

NCT ID: NCT00428545 Completed - Lymphoma Clinical Trials

Bevacizumab and Bortezomib in Patients With Advanced Malignancy

Start date: January 2007
Phase: Phase 1
Study type: Interventional

The goal of this clinical research study is to find the highest tolerable dose of Avastin™ (bevacizumab) and Velcade™ (bortezomib) that can be given in combination to patients with a metastatic or unresectable advanced malignancy. The safety and effectiveness of this drug combination will also be studied.

NCT ID: NCT00428285 Completed - HIV Infections Clinical Trials

Tolerability, Safety, & Efficacy of Argon Plasma Coagulation to Treat Anal Intraepithelial Neoplasia in HIV-Positive Men

Start date: February 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess if argon plasma coagulation (APC) is a safe and well tolerated treatment method for anal intraepithelial neoplasia (AIN) grade 2/3 in HIV-positive men having sex with men (MSM).