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Breast Neoplasms clinical trials

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NCT ID: NCT00334139 Completed - Breast Cancer Clinical Trials

Effect of Zoledronic Acid on Bone Metabolism in Patients With Bone Metastasis and Prostate or Breast Cancer

Start date: May 2006
Phase: Phase 4
Study type: Interventional

Bisphosphonates have been used extensively in the treatment and the prevention of skeletal complications associated with bone metastases in patients with breast cancer and prostate cancer. The purpose of this study is to assess the effect of zoledronic acid patients with prostate cancer or breast cancer and bone metastasis.

NCT ID: NCT00333775 Completed - Breast Cancer Clinical Trials

A Study of Bevacizumab (Avastin) in Women With HER2 Negative Metastatic Breast Cancer

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

This study will evaluate the efficacy and safety of 2 doses of Avastin in combination with docetaxel, versus docetaxel plus placebo, in patients with metastatic HER2 negative breast cancer who are candidates for taxane-based chemotherapy but who have not received prior chemotherapy for metastatic disease. The anticipated time on treatment is 1-2 years and the target sample size is 500+ individuals.

NCT ID: NCT00333229 Terminated - Clinical trials for Primary Hormone Receptor Negative Breast Cancer in Premenopausal Women

A Study of Zoledronic Acid in the Prevention of Cancer Therapy-induced Bone Loss

Start date: March 2006
Phase: Phase 4
Study type: Interventional

Breast cancer and osteoporosis are two of the most frequent diseases in women. Estrogen may be associated with bone loss and the risk of breast cancer because of its potent effects on the mitotic activity of breast epithelium and on bone turnover. This study is will assess the safety and efficacy of Zoledronic acid 4 mg, given every 3 months over 24 months, in improving bone mineral density in premenopausal women with hormone receptor negative breast cancer and adjuvant chemotherapeutic treatment compared to placebo. This study is not recruiting patients in the United States.

NCT ID: NCT00333047 Completed - Clinical trials for Metastatic Breast Cancer

Letrozole in Metastatic Breast Cancer in Combination With Chemotherapy

Start date: July 2002
Phase: Phase 2/Phase 3
Study type: Interventional

Therapeutic interventions for patients with metastatic breast cancer are aimed at prolonging survival and improving the quality of life. The objective of this trial is to assess if an initial chemotherapy followed by an endocrine therapy leads to a longer disease-free interval as compared to chemotherapy alone.

NCT ID: NCT00332852 Completed - Breast Cancer Clinical Trials

Letrozole as Early Adjuvant Treatment of Postmenopausal Patients With Primary Breast Cancer

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

This is a prospective open-label one-arm phase III trial designed to evaluate the safety and efficacy of letrozole 2.5 mg administered orally daily for 24 months as adjuvant therapy in postmenopausal patients with primary breast cancer. This trial is not recruiting patients in the United States.

NCT ID: NCT00332709 Completed - Osteoporosis Clinical Trials

Safety/Efficacy of Letrozole Monotherapy or in Combination With Zoledronic Acid as Extended Adjuvant Treatment of Postmenopausal Patients With Primary Breast Cancer

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

This was a prospective, randomized, open-label, two arm phase III trial designed to evaluate the efficacy and safety of zoledronic acid in preventing bone loss in postmenopausal women with operable breast cancer who had received 4 to 6 years of adjuvant tamoxifen therapy after resection of the tumor. Patients were treated with letrozole 2.5 mg orally per day or letrozole 2.5 mg orally per day in combination with zoledronic acid 4 mg/6 months as an infusion. This trial did not recruit patients in the United States.

NCT ID: NCT00331942 Recruiting - Breast Cancer Clinical Trials

Breast Cancer Associated Antibodies

Start date: July 2006
Phase: N/A
Study type: Observational

To determine the ability of the Cimmunology process to lead to in vitro antibody production, the ability of the ELISA assays to detect any of those antibodies, and to establish the relationship between the ELISA results and the clinical / pathological status of the patient. The statistical significance of the CAAb test results will be determined.

NCT ID: NCT00331630 Completed - Breast Cancer Clinical Trials

Abraxane and Lapatinib in Treating Patients With Stage I, Stage II, or Stage III Breast Cancer

Start date: May 4, 2006
Phase: Early Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as Abraxane, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Lapatinib may stop the growth of tumor cells by blocking some of the enzymes needed for their growth. Giving Abraxane together with lapatinib may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving Abraxane together with lapatinib works in treating patients with stage I, stage II, or stage III breast cancer.

NCT ID: NCT00331552 Completed - Clinical trials for HER2-positive Breast Cancer

Doxorubicin Hydrochloride Liposome, Cyclophosphamide, and Trastuzumab in Treating Patients With Stage IV Breast Cancer

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

Drugs used in chemotherapy, such as doxorubicin hydrochloride liposome and cyclophosphamide, 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 trastuzumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Giving more than one drug (combination chemotherapy) together with trastuzumab may be a better way to block tumor growth.

NCT ID: NCT00331097 Completed - Breast Cancer Clinical Trials

ELDA: Elderly Breast Cancer - Docetaxel in Adjuvant Treatment

Start date: July 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare disease free survival of elderly breast cancer patients treated with standard adjuvant chemotherapy (CMF) versus experimental adjuvant chemotherapy (weekly docetaxel).