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Endometrial Neoplasms clinical trials

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NCT ID: NCT01068483 Completed - Breast Cancer Clinical Trials

Safety of BKM120 Monotherapy in Advanced Solid Tumor Patients

Start date: November 2008
Phase: Phase 1
Study type: Interventional

This is a first-in-man, phase I clinical research study with BKM120, a potent and highly specific oral pan-class I phosphatidylinositol-3-kinase (PI3K) inhibitor. The study consists of a dose escalation part followed by a MTD expansion part. Once the MTD has been defined, the MTD expansion part will be opened for enrollment.

NCT ID: NCT01068249 Active, not recruiting - Endometrial Cancer Clinical Trials

Letrozole and RAD001 With Advanced or Recurrent Endometrial Cancer

Start date: April 30, 2010
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if the combination of RAD001 (everolimus) and Femara (letrozole) can help to control recurrent or progressive endometrial cancer. The safety of this drug combination will also be studied.

NCT ID: NCT01065662 Completed - Ovarian Cancer Clinical Trials

AZD2171 and Temsirolimus in Patients With Advanced Gynecological Malignancies

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

The purpose of this research study is to determine the safety of the combination of the two drugs cediranib and temsirolimus and the highest doses of these two drugs that can be given in combination to people safely. Cediranib is a drug that may stop blood supply to the tumor and therefore help keep cancer cells from growing. Temsirolimus is a drug that may stop cancer cells from growing. These drugs have been used in other research studies in ovarian and kidney cancer and these studies suggest that these drugs may help to keep cancer from growing in this research study.

NCT ID: NCT01049126 Completed - Endometrial Cancer Clinical Trials

Retrospective Case Study Examining Patient Outcomes Compared to the ChemoFx Assay in Endometrial Cancer Patients

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

The purpose of this study is to assess the relationship of assay sensitive patients versus assay resistant patients with progression free survival.

NCT ID: NCT01045187 Completed - Endometrial Cancer Clinical Trials

Feasibility Study Using the Xoft System for the Treatment of Endometrial Cancer

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

Multicenter, non-randomized, feasibility study to evaluate the treatment and assess acute safety of the FDA Cleared Axxent Electronic Brachytherapy System and vaginal applicator for intracavitary vaginal cuff treatment according to the physician's current standard of care.

NCT ID: NCT01041027 Terminated - Clinical trials for Endometrial Adenocarcinoma

Radiation Therapy, Paclitaxel, and Carboplatin in Treating Patients With High-Risk Endometrial Cancer

Start date: January 16, 2009
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well radiation therapy, paclitaxel, and carboplatin work in treating patients with high-risk endometrial cancer. Radiation therapy uses high energy x rays to kill tumor cells. Drugs used in chemotherapy, such as paclitaxel and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing or by stopping them from spreading. Giving radiation therapy with chemotherapy may kill more tumor cells.

NCT ID: NCT01013324 Completed - Endometrial Cancer Clinical Trials

Study of XL147 (SAR245408) in Advanced or Recurrent Endometrial Carcinoma

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

There has not been any systemic therapy approved in the United States or in Europe for treating advanced or recurrent endometrial cancer (EC). This study will evaluate the safety and preliminary efficacy of XL147 in advanced or recurrent EC. Constitutively active phosphatidylinositol-3 kinase (PI3K)/phosphatase and tensin homolog on chromosome 10 (PTEN) pathway signaling is common in EC and involved in the development and/or progression of the disease. PTEN deficiency and/or activating mutations/amplification in the PIK3CA gene that encodes the p110α catalytic subunit of PI3K have been frequently detected in EC patients. XL147 is a potent and highly selective inhibitor of the Class I PI3K family of lipid kinases. In addition, in vivo preclinical data have demonstrated that XL147 targets both proximal and distal signaling in the PI3K/PTEN pathway. Therefore, XL147 may have utility in the treatment of subjects with advanced or recurrent EC.

NCT ID: NCT01005329 Completed - Clinical trials for Endometrial Adenocarcinoma

Intensity-Modulated Radiation Therapy, Cisplatin, and Bevacizumab Followed by Carboplatin and Paclitaxel in Treating Patients Who Have Undergone Surgery for Endometrial Cancer

Start date: November 6, 2009
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side effects of giving intensity-modulated radiation therapy together with cisplatin and bevacizumab followed by carboplatin and cisplatin and to see how well they work in treating patients who have undergone surgery for high-risk endometrial cancer. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Drugs used in chemotherapy, such as cisplatin, 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. Monoclonal antibodies, such as bevacizumab, can block the ability of tumor cells to grow and spread. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving intensity-modulated radiation therapy together with chemotherapy and bevacizumab after surgery may kill any tumor cells that remain after surgery.

NCT ID: NCT00997373 Completed - Clinical trials for Endometrial Carcinoma

Letrozole as a Treatment of Endometrial Cancer

Start date: October 2009
Phase: N/A
Study type: Interventional

Some cases of endometrial cancer are dependent on estrogen for their growth. Letrozole blocks estrogen production in the body. The purpose of this study is to determine if the investigators can predict which patients might benefit from Letrozole treatment by studying the many different forms of the estrogen receptor molecule that exist within the cancer tissues. To participate in this study, the patients must be 40 years of age or older and have biopsy-proven endometrial carcinoma, either well differentiated or moderately differentiated forms. Also, to be eligible to participate in this study, the patients need to be healthy enough to have a hysterectomy. If the patients are less than age 60, they will need a blood test (FSH) to confirm that they have gone into menopause.

NCT ID: NCT00987051 Completed - Clinical trials for Endometrial Neoplasms

Sentinel Node and Endometrial Cancer

Senti-Endo
Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the relevance of sentinel node in endometrial cancer. Sentinel node is thought to reflect the status of lymph node. Only 10 to 20% of women with endometrial cancer exhibit lymph node metastasis hence systematic lymphadenectomy is questionable. In breast cancer, melanoma and vulvar cancer, sentinel node has emerged as an alternative to complete lymphadenectomy.