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Breast Neoplasms clinical trials

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NCT ID: NCT02141139 Not yet recruiting - Breast Neoplasms Clinical Trials

Perioperative Inflammation and Breast Cancer Outcome

Start date: September 2014
Phase: Phase 3
Study type: Interventional

It is increasingly recognized the NSAIDS (nonsteroidal antiinflammatory drug) might prevent the several cancers. In breast cancer, the role of NSAIDS (nonsteroidal antiinflammatory drug) has been suggested.However, there was no consistent results. surgery is main cause of inflammation for cancer patients. Therefore, we want to know the association between prevention of perioperative inflammation with NSAIDS and breast cancer outcomes.

NCT ID: NCT02140437 Withdrawn - Clinical trials for Carcinoma Breast Stage IV

Fulvestrant Combined Anastrozole Versus Anastrozole in Luminal A-like Postmenopausal ABC

Start date: March 2014
Phase: Phase 2
Study type: Interventional

This research is designed to investigate whether the addition of fulvestrant 500mg to anastrozole is better than anastrozole alone as first-line endocrine therapy for advanced breast cancer.

NCT ID: NCT02139358 Completed - Breast Cancer Clinical Trials

Phase I/IIa Trial of Gemcitabine Plus Trastuzumab and Pertuzumab in Previously Treated Metastatic HER2+ Breast Cancer

Start date: September 5, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and activity of gemcitabine plus trastuzumab and pertuzumab in patients with metastatic human epidermal growth factor receptor 2 (HER2)+ breast cancer who have progressed on at least one prior line of chemotherapy plus HER2 targeted agent such as T-DM1, trastuzumab, or lapatinib.

NCT ID: NCT02137837 Terminated - Breast Cancer Clinical Trials

S1222 Trial (Everolimus, Anastrozole and Fulvestrant) in Post-Menopausal Stage IV Breast Cancer

Start date: May 2014
Phase: Phase 3
Study type: Interventional

This randomized Phase III trial studies how well the combination of fulvestrant and everolimus together or the combination of anastrozole, fulvestrant and everolimus together, improve progression-free survival (PFS) versus fulvestrant alone.

NCT ID: NCT02137252 Terminated - Clinical trials for Ductal Carcinoma in Situ

Naltrexone RCT for Treatment-Emergent Fatigue in Patients Receiving Radiation Therapy for Breast Cancer

Start date: May 2014
Phase: Phase 2
Study type: Interventional

Naltrexone is a drug which blocks some effects of chemicals called beta-endorphins that are made in the body. Beta-endorphins can be made in response to stress, injury, and also pleasurable activities. In previous studies, it has been shown that levels of beta-endorphins in the blood go up during radiation therapy, and that this increase is linked to fatigue. This suggests that naltrexone may help to reduce fatigue in people who are getting radiation therapy In this research study, the investigators are looking to see whether naltrexone works better than a placebo in reducing fatigue during radiation therapy.

NCT ID: NCT02137083 Completed - Clinical trials for Metastatic Breast Cancer

A Trial Comparing Docetaxel Plus Fulvestrant With Docetaxel in Metastatic Breast Cancer

Start date: April 2014
Phase: Phase 2
Study type: Interventional

Comparing Docetaxel Plus Fulvestrant With Docetaxel in Patients With Metastatic Breast Cancer

NCT ID: NCT02136927 Terminated - Breast Cancer Clinical Trials

Bioavailability Study of SPARC1210 and Reference1210 in Subjects With Metastatic Breast Cancer

Start date: August 2014
Phase: Phase 1
Study type: Interventional

Pharmacokinetic, bioequivalence study

NCT ID: NCT02135159 Completed - Clinical trials for HER2-positive Breast Cancer

Patients With Brain Metastases From HER2-positive Breast Cancer

BIRTH
Start date: February 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the optimal sequences of combined trastuzumab emtansine (T-DM1) and whole-brain radiotherapy in patients presenting brain metastases from HER2-positive breast cancer in terms of acute toxicities and blood/cerebrospinal fluid T-DM1 pharmacokinetics.

NCT ID: NCT02134977 Completed - Breast Cancer Clinical Trials

Leuprorelin Acetate SR 11.25 mg Injection Kit Specified Drug-use Survey: "QOL Survey in Premenopausal Breast Cancer Patients"

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

The purpose of this survey is to examine the effect on QOL improvement and convenience of switching to Leuprorelin acetate 3 moths depot 11.25 mg Injection Kit (Leuplin SR 11.25 mg Injection Kit) from a 4-week adjuvant therapy with a LH-RHa 1 month depot over 48 weeks in premenopausal breast cancer patients in daily medical practice. Influence of condition of estrogen receptor expression on the efficacy and safety of Leuprorelin acetate SR 11.25 mg Injection Kit was also evaluated.

NCT ID: NCT02133677 Not yet recruiting - Clinical trials for Lung Cancer and Breast Cancer Patients With Brain Metastases

A Phase II Multi-center Pilot Study of Concurrent Temozolomide and Whole Brain Irradiation in Lung Cancer and Breast Cancer Patients With Brain Metastases

Start date: May 2014
Phase: Phase 2
Study type: Interventional

Brain metastasis (BM) is among the most feared complications in cancer because even small tumors may cause incapacitating neurologic symptoms. It is observed in more than 50% of patients with lung cancer and 15% to 25% of patients with breast cancer. Temozolomide (TMZ) is an oral alkylating agent that crosses blood-brain barrier (BBB). This pilot study aims to evaluate the efficacy, safety and tolerability of whole-brain radiotherapy (WBRT) plus concomitant TMZ in lung cancer and breast cancer patients with BM.