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Breast Neoplasms clinical trials

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NCT ID: NCT02950259 Active, not recruiting - Clinical trials for Triple Negative Breast Cancer

Pre-operative IRX-2 in Early Stage Breast Cancer (ESBC)

Start date: February 9, 2017
Phase: Phase 1
Study type: Interventional

The goal of this study is assess the safety and tolerability of the IRX-2 regimen in patients with early stage breast cancer (ESBC) and to estimate the pathologic complete response rate to neoadjuvant anthracycline-based and non-platinum containing chemotherapy in patients with triple-negative breast cancer who have received the IRX-2 Regimen before chemotherapy.

NCT ID: NCT02950064 Active, not recruiting - Breast Neoplasms Clinical Trials

A Study to Determine the Safety of BTP-114 for Treatment in Patients With Advanced Solid Tumors With BRCA Mutations

Start date: September 2016
Phase: Phase 1
Study type: Interventional

This is a phase 1, Open-label, multicenter Dose Escalation study of BTP-114, a novel platinum product, in patients with advanced solid tumors and BRCA or other DNA repair mutation. This clinical study is comprised of 2 sequential parts: Part 1 (Dose Escalation) and Part 2 (Expansion). The purpose of this study is to evaluate the safety, pharmacokinetics and the anti-cancer activity of BTP-114.

NCT ID: NCT02949167 Active, not recruiting - Breast Cancer Clinical Trials

MyHealth: Follow-up After Breast Cancer Treatment

MyHealth
Start date: November 2016
Phase: N/A
Study type: Interventional

Approximately 24,000 women attend a follow-up care program after end of primary treatment for breast cancer (BC) in Denmark. There is no well-conducted, larger randomized controlled trials (RCT) outlining a gold standard for follow-up programs ensuring early detection of recurrence, good management of symptoms and cost-effectiveness. The primary aim of this randomised, controlled trial is to test whether a nurse-led individually tailored symptom management program (MyHealth) will significantly reduce reported symptoms among BC patients following primary treatment compared to physician-led scheduled follow-up. Secondary, the investigators will examine patient activation (self-management), anxiety, depression, fear of recurrence, work ability, time to recurrence, overall survival, health behavior changes, health care utilization and financial costs in the two arms. The MyHealth program provides patients with a nurse-led education focusing on management of symptoms, an electronic platform to report symptoms to the nurses and support in symptom management and navigation of patients to appropriate health care services.

NCT ID: NCT02947685 Active, not recruiting - Clinical trials for HER-2 Positive Breast Cancer

Randomized, Open Label, Clinical Study of the Targeted Therapy, Palbociclib, to Treat Metastatic Breast Cancer

PATINA
Start date: June 21, 2017
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to demonstrate that the combination of palbociclib with anti-HER2 therapy plus endocrine therapy is superior to anti-HER2-based therapy plus endocrine therapy alone in improving the outcomes of subjects with hormone receptor-positive, HER2+ metastatic breast cancer.

NCT ID: NCT02942615 Active, not recruiting - Breast Neoplasms Clinical Trials

The Safety Management of Cardiac Toxicity in Breast Cancer Patients Under Multidiscipline Therapy.

Start date: June 27, 2017
Phase: N/A
Study type: Interventional

This trial is to explore the optimal strategies for guaranteeing the cardiac safety of breast cancer patients following adjuvant radiotherapy in the modern era of multidisciplinary treatment.

NCT ID: NCT02942355 Active, not recruiting - Breast Cancer Clinical Trials

Trial of Anastrozole and Palbociclib in Metastatic HER2-Negative Breast Cancer

Start date: December 7, 2016
Phase: Phase 2
Study type: Interventional

This is an open-label, pilot study designed to evaluate the safety and feasibility of combining anastrozole and palbociclib in the following two cohorts: Cohort A) as first-line therapy and Cohort B) as maintenance therapy after first-line chemotherapy in postmenopausal patients with HR-positive, HER2-negative metastatic breast cancer. Pre- and perimenopausal women must receive therapy with an LHRH agonist. The LHRH agonist will be by choice for an approved LHRH agonist administered according to its respective prescribing information. Following informed consent and eligibility check, subjects will be enrolled to either Cohort A or Cohort B.

NCT ID: NCT02926196 Active, not recruiting - Clinical trials for Triple Negative Breast Neoplasms

Adjuvant Treatment for High-risk Triple Negative Breast Cancer Patients With the Anti-PD-l1 Antibody Avelumab

A-Brave
Start date: June 17, 2016
Phase: Phase 3
Study type: Interventional

Phase III randomized trial of the anti-PD-L1 antibody avelumab as adjuvant or post-neoadjuvant treatment for high-risk triple negative breast cancer patients. The overall protocol-defined patient population will include the following two strata of patients: - Stratum A - Patients who have completed treatment with curative intent including surgery of the primary tumor followed by adjuvant chemotherapy . - Stratum B - Patients who have completed treatment with curative intent including neoadjuvant chemotherapy followed by surgery of the primary tumor and (if indicated) further adjuvant chemotherapy.

NCT ID: NCT02918084 Active, not recruiting - Breast Cancer Clinical Trials

CONcurrent vs SEqueNTial Adjuvant Treatments in Early Breast Cancer

GIM10-CONSENT
Start date: June 2013
Phase: Phase 3
Study type: Interventional

Breast cancer is the most common form of cancer among women. For patients candidated for adjuvant chemotherapy and endocrine therapy the optimal timing for their has not been clearly defined yet.

NCT ID: NCT02913430 Active, not recruiting - Clinical trials for Metastatic Breast Cancer

Treatment of Metastatic Breast Cancer With Fulvestrant Plus Palbociclib or Tamoxifen Plus Palbociclib

Start date: April 24, 2018
Phase: Early Phase 1
Study type: Interventional

To assess longitudinal changes in allele frequency of ESR1 mutation in plasma in patients treated with Fulvestrant plus palbociclib compared to tamoxifen plus palbociclib

NCT ID: NCT02909361 Active, not recruiting - Clinical trials for Metastatic Breast Cancer

Fulvestrant 500mg in Patients With Advanced Breast Cancer

Start date: October 11, 2017
Phase:
Study type: Observational [Patient Registry]

Fulvestrant 500mg in Patients With Advanced Breast Cancer