Clinical Trials for Breast Cancer

Currently registered clinical trials for Breast Cancer from ClinicalTrials.gov. 20 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Breast Cancer from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 20
  • Active, not recruiting: 9
  • Completed: 12
  • Other: 9

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT01174121 — Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment332
Study TypeINTERVENTIONAL
ConditionsMetastatic Colorectal Cancer; Metastatic Pancreatic Cancer; Metastatic Ovarian Cancer; Metastatic Breast Carcinoma; Metastatic Endocrine Tumors/ Neuroendocrine Tumors
Interventions; ;

Background:

The NCI Surgery Branch has developed an experimental therapy that involves taking white blood cells from patients’ tumors, growing them in the laboratory in large numbers, and then giving the cells back to the patient. These cells are called Tumor Infiltrating Lymphocytes, or TIL and we have given this type of treatment to over 200 patients with melanoma. Researchers want to know i…

NCT02595957 — Genomic Services Research Program

StatusRecruiting
PhaseN/A
SponsorNational Human Genome Research Institute (NHGRI)
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsColon Cancer; Breast Cancer

Background:

Genes are the instructions a person s body uses to function. Genome sequencing reads through all of a person s genes. Everyone has many gene variants, and most do not cause disease. Some gene variants called secondary findings may be important for a person s health even if they are not related to the reason why a person had genome sequencing done. Researchers want to learn more abo…

NCT04222413 — Metarrestin (ML-246) in Subjects With Metastatic Solid Tumors

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment116
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Tumors; Metastatic Pancreatic Cancer; Pediatric Solid Tumor; Advanced Breast Cancer; Malignant Peripheral Nerve Sheath Tumor
Interventions

Background:

Metastasis is the spread of cancer from one organ to a nonadjacent organ. It causes 90% of cancer deaths. No treatment specifically prevents or reduces metastasis. Researchers hope a new drug can help. It stops cancer cells from growing and spreading further and possibly shrink cancer lesions in distant organs.

Objective:

To find a safe dose of metarrestin and to see if this dose…

NCT05564377 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Locally Advanced or Advanced Solid Tumors, The ComboMATCH Screening Trial

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment2900
Study TypeINTERVENTIONAL
ConditionsAdvanced Malignant Solid Neoplasm; Anatomic Stage III Breast Cancer AJCC v8; Anatomic Stage IV Breast Cancer AJCC v8; Locally Advanced Malignant Solid Neoplasm; Malignant Female Reproductive System Neoplasm
Interventions; ;

This ComboMATCH patient screening trial is the gateway to a coordinated set of clinical trials to study cancer treatment directed by genetic testing. Patients with solid tumors that have spread to nearby tissue or lymph nodes (locally advanced) or have spread to other places in the body (advanced) and have progressed on at least one line of standard systemic therapy or have no standard treatmen…

NCT06058377 — Adding an Immunotherapy Drug, MEDI4736 (Durvalumab), to the Usual Chemotherapy Treatment (Paclitaxel, Cyclophosphamide, and Doxorubicin) for Stage II-III Breast Cancer

StatusRecruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment3680
Study TypeINTERVENTIONAL
ConditionsAnatomic Stage II Breast Cancer AJCC v8; Anatomic Stage III Breast Cancer AJCC v8; HER2-Negative Breast Carcinoma; Hormone Receptor-Positive Breast Carcinoma
Interventions; ;

This phase III trial compares the addition of an immunotherapy drug (durvalumab) to usual chemotherapy versus usual chemotherapy alone in treating patients with MammaPrint High 2 Risk (MP2) stage II-III hormone receptor positive, HER2 negative breast cancer. Immunotherapy with monoclonal antibodies, such as durvalumab, may help the body’s immune system attack the cancer, and may interfere with …

NCT05827081 — Phase IIIb Study of Ribociclib + ET in Early Breast Cancer

StatusRecruiting
PhasePhase 3
SponsorNovartis Pharmaceuticals
Enrollment1400
Study TypeINTERVENTIONAL
ConditionsEarly Breast Cancer
Interventions; ;

The purpose of this open-label, multicenter, phase IIIb, single-arm study is to characterize the efficacy and safety of the combination of ribociclib and standard adjuvant endocrine therapy (ET) on invasive breast cancer-free survival (iBCFS), in a close to clinical practice patient population with HR-positive (HR+), HER2-negative (HER2-), Anatomic Stage Group III, IIB, and a subset of Stage II…

NCT06492616 — A Study of Elacestrant Versus Standard Endocrine Therapy in Women and Men With ER+,HER2-, Early Breast Cancer With High Risk of Recurrence

StatusRecruiting
PhasePhase 3
SponsorStemline Therapeutics, Inc.
Enrollment4220
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions; ;

The primary goal of this study is to evaluate the effectiveness of elacestrant versus standard endocrine therapy in participants with node-positive, Estrogen Receptor-positive (ER+), Human Epidermal Growth Factor-2 negative (HER2-) early breast cancer with high risk of recurrence.

NCT06551116 — QuantifyHER: Quantitative Immunofluorescence and/or RT-qPCR for Measuring HER2 in HER2-low Metastatic Breast Cancer

StatusRecruiting
PhaseN/A
SponsorAbramson Cancer Center at Penn Medicine
Enrollment200
Study TypeOBSERVATIONAL
ConditionsHER2-positive Metastatic Breast Cancer
Interventions

This study will assess whether a quantitative, HER2 assay can accurately and reliably discriminate between responders and non-responders among patients with HER2 IHCI+ metastatic breast cancer who are receiving T-Dxd.

NCT06444269 — Precision Medicine in Action: Phase II Trial of Response Adaptive Ablative Pre-operative SPBI (RAPS) and Non-operative Sentinel Lymph Node Biopsy in Patients With Early-stage ER+ Breast Cancer: RAPS Trial

StatusRecruiting
PhasePhase 2
SponsorUniversity of Texas Southwestern Medical Center
Enrollment53
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions;

1. Efficacy of PULSAR preoperative radiation 2. Evaluate potential of microbubble CEUS as an alternative to operative SLNBx 3. Evaluate potential of OA to evaluate treatment response of pre-operative radiation on the tumor

NCT06562192 — Phase I Study of [177Lu]Lu-NNS309 in Patients With Pancreatic, Lung, Breast and Colorectal Cancers

StatusRecruiting
PhasePhase 1
SponsorNovartis Pharmaceuticals
Enrollment162
Study TypeINTERVENTIONAL
ConditionsPancreatic Ductal Adenocarcinoma; Non-small Cell Lung Cancer; HR+/HER2- Ductal and Lobular Breast Cancer; Triple Negative Breast Cancer; Colorectal Cancer
Interventions;

The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of [177Lu]Lu-NNS309 and the safety and imaging properties of [68Ga]Ga-NNS309 in patients aged ≥ 18 years with locally advanced or metastatic pancreatic ductal adenocarcinoma (PDAC), non-small cell lung cancer (NSCLC), HR+/HER2- ductal and lobular breast cancer (BC), triple negative breast c…

NCT06830720 — A Non-interventional Study for Kisqali (Ribociclib) in Combination With an Aromatase Inhibitor for Adjuvant Treatment in Patients With HR+/HER2- Early Breast Cancer at High Risk of Recurrence

StatusRecruiting
PhaseN/A
SponsorNovartis Pharmaceuticals
Enrollment3250
Study TypeOBSERVATIONAL
ConditionsBreast Neoplasms
Interventions; ;

This non-interventional observational study evaluates the real-world effectiveness and safety profile of ribociclib in combination with an aromatase inhibitor for adjuvant treatment in patients with HR+/HER2- early breast cancer at high risk of recurrence, as well as patient compliance and quality of life.

NCT06995898 — The Vanguard Study: Testing a New Way to Screen for Cancer

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment24000
Study TypeINTERVENTIONAL
ConditionsBladder Carcinoma; Breast Carcinoma; Colorectal Carcinoma; Esophageal Carcinoma; Gastric Carcinoma
Interventions; ;

The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden o…

NCT07017673 — Phase II Trial of Ivonescimab in Combination With Carboplatin + Docetaxel in Patients With Early-Stage Triple Negative Breast Cancer

StatusRecruiting
PhasePhase 2
SponsorCedars-Sinai Medical Center
Enrollment34
Study TypeINTERVENTIONAL
ConditionsTNBC; TNBC - Triple-Negative Breast Cancer; Early Stage Triple-Negative Breast Carcinoma
Interventions; ;

This is a single arm phase II trial combination of ivonescimab and carbo-docetaxel every 3 weeks for 6 cycles in patients with early-stage triple negative breast cancer. The trial is designed to test the safety and efficacy of adding ivonescimab in patients with early TNBC undergoing neoadjuvant chemotherapy with carboplatin and docetaxel. Patients will receive ivonescimab 20 mg/kg IV on Day 1 …

NCT06982521 — Phase 3 Study of RLY-2608 + Fulvestrant vs Capivasertib + Fulvestrant as Treatment for Locally Advanced or Metastatic PIK3CA-mutant HR+/HER2- Breast Cancer

StatusRecruiting
PhasePhase 3
SponsorRelay Therapeutics, Inc.
Enrollment540
Study TypeINTERVENTIONAL
ConditionsPIK3CA Mutation; HER2- Negative Breast Cancer; Hormone Receptor Positive Tumor; Breast Cancer; Metastatic Breast Cancer
Interventions; ;

This is a global, multicenter, open-label, randomized Phase 3 study comparing the efficacy and safety of RLY-2608 + fulvestrant to capivasertib + fulvestrant for the treatment of patients with HR+/HER2- ABC with PIK3CA mutation following recurrence or progression on or after treatment with a CDK4/6 inhibitor.

NCT07671885 — Evaluating the Response-Guided Therapy With Neoadjuvant Endocrine Therapy to Optimize Adjuvant Treatment in Premenopausal HR+/HER2- Breast Cancer (JCOG2402, Young HOPE)

StatusRecruiting
PhasePhase 3
SponsorTokyo Women’s Medical University
Enrollment950
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions;

Young HOPE/JCOG2402 is a multicenter, randomized phase III study designed to evaluate response-guided therapy following neoadjuvant endocrine therapy to optimize adjuvant treatment in premenopausal HR+/HER2- Breast Cancer.

Premenopausal women with intermediate-risk HR-positive/HER2-negative breast cancer derive benefit from the addition of chemotherapy to endocrine therapy. However, previous s…

NCT07264790 — Assessment of Topical Minoxidil on Intraoperative Flap Perfusion and Cutaneous Flap Viability in Breast Recon

StatusRecruiting
PhasePhase 1
SponsorDuke University
Enrollment25
Study TypeINTERVENTIONAL
ConditionsBreast Reconstruction; Perfusion; Complications; High Risk for Breast Cancer; Genetic Predisposition
Interventions;

The purpose of the study is to determine whether pharmacologic delay using minoxidil in patients undergoing bilateral risk reducing mastectomy with reconstruction could achieve improvement in flap perfusion and flap viability at the time of surgery. Patients will undergo randomization of their breasts to determine which breast will receive the experimental intervention and which breast will ser…

NCT07528716 — Artificial Intelligence Model-Guided Neoadjuvant Anti-HER2 Targeted Therapy

StatusRecruiting
PhasePhase 3
SponsorFudan University
Enrollment280
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions; ;

Based on total pathologic complete response (tpCR) after surgery, to evaluate the efficacy of an artificial intelligence model-matched anti-HER2 targeted treatment strategy (investigational arm) versus nab-paclitaxel + carboplatin + trastuzumab + pertuzumab (PCbHP, control arm) as neoadjuvant therapy for patients with early or locally advanced human epidermal growth factor receptor 2 (HER2)-pos…

NCT07624617 — Fast-Her: Fasting Effects on Breast Cancer Treatment

StatusRecruiting
PhaseN/A
SponsorUniversity of Minnesota
Enrollment15
Study TypeINTERVENTIONAL
ConditionsMetastatic Breast Cancer
Interventions

We hypothesize that promoting a fasting state will strengthen the anti-cancer effects of PI3K inhibitors in metastatic breast cancer (MBC) treatment. The primary objective of this study is to assess acceptability of prolonged fasting in this population.

NCT07460752 — Evaluation of Alternative Site Goserelin Acetate Injection for Ovarian Function Suppression (OFS) in Local and Locally Advanced Premenopausal Hormone Receptor Positive Breast Cancer Patients

StatusRecruiting
PhasePhase 2
SponsorMayo Clinic
Enrollment98
Study TypeINTERVENTIONAL
ConditionsAnatomic Stage I Breast Cancer AJCC v8; Anatomic Stage II Breast Cancer AJCC v8; Anatomic Stage III Breast Cancer AJCC v8; Locally Advanced Hormone Receptor-Positive Breast Carcinoma
Interventions; ;

This phase II trial determines if giving goserelin acetate injections in the upper gluteal region is as effective for ovarian function suppression (OFS) as giving injections in the abdomen for ovarian function suppression (OFS) in premenopausal patients with hormone receptor positive breast cancer that has not spread to other parts of the body (localized) or that has spread to nearby tissue or …

NCT07681323 — Timing of ctDNA Testing in HR+/HER2- Advanced Breast Cancer

StatusRecruiting
PhaseN/A
SponsorGeneplus-Beijing Co. Ltd.
Enrollment400
Study TypeOBSERVATIONAL
ConditionsAdvanced Breast Cancer

This multicenter, prospective observational cohort study aims to investigate the impact of circulating tumor DNA (ctDNA) level and key actionable gene mutation status on prognosis and treatment response in patients with advanced hormone receptor-positive / human epidermal growth factor receptor 2-negative (HR+/HER2-) breast cancer.

Active, Not Recruiting

NCT02484404 — Phase I/II Study of the Anti-Programmed Death Ligand-1 Durvalumab Antibody (MEDI4736) in Combination With Olaparib and/or Cediranib for Advanced Solid Tumors and Advanced or Recurrent Ovarian, Triple Negative Breast, Lung, Prostate and Colorectal Can…

StatusActive, not recruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment268
Study TypeINTERVENTIONAL
ConditionsColorectal Neoplasms; Breast Neoplasms
Interventions; ;

Background:

- Durvalumab is a drug that may help people s immune systems respond to and kill cancer cells. Olaparib is a drug that may inhibit repairing DNA damage of cancer cells. Cediranib is a drug that may stop the blood vessel growth of cancer cells. This study has two components. In the phase 1 component of the study, researchers want to investigate how well participants tolerate the co…

NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment6452
Study TypeINTERVENTIONAL
ConditionsAdvanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma
Interventions; ;

This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…

NCT02445391 — Platinum in Treating Patients With Residual Triple-Negative Breast Cancer Following Neoadjuvant Chemotherapy

StatusActive, not recruiting
PhasePhase 3
SponsorECOG-ACRIN Cancer Research Group
Enrollment415
Study TypeINTERVENTIONAL
ConditionsEstrogen Receptor Negative; HER2/Neu Negative; Invasive Breast Carcinoma; Progesterone Receptor Negative; Stage II Breast Cancer
Interventions; ;

This randomized phase III trial studies how well cisplatin or carboplatin (platinum based chemotherapy) works compared to capecitabine in treating patients with remaining (residual) basal-like triple-negative breast cancer following chemotherapy after surgery (neoadjuvant). Drugs used in chemotherapy, such as cisplatin, carboplatin and capecitabine, work in different ways to stop the growth of …

NCT03747120 — Neoadjuvant Her2-targeted Therapy and Immunotherapy With Pembrolizumab [IIT2018-04-MCARTHUR-NEOHP]

StatusActive, not recruiting
PhasePhase 2
SponsorUniversity of Texas Southwestern Medical Center
Enrollment138
Study TypeINTERVENTIONAL
ConditionsHER2-positive Breast Cancer; Breast Cancer
Interventions; ;

A phase 2 open-label, randomized, multi-center trial to evaluate the efficacy and safety of neoadjuvant trastuzumab, pertuzumab and weekly paclitaxel (THP) as compared to neoadjuvant trastuzumab, pertuzumab, pembrolizumab and weekly paclitaxel (THP-pembrolizumab), or neoadjuvant trastuzumab, pembrolizumab and weekly paclitaxel (TH-pembrolizumab ) in chemo naive patients with invasive human epid…

NCT04521686 — Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 or IDH2 Mutations

StatusActive, not recruiting
PhasePhase 1
SponsorEli Lilly and Company
Enrollment200
Study TypeINTERVENTIONAL
ConditionsCholangiocarcinoma; Chondrosarcoma; Glioma; Any Solid Tumor
Interventions; ;

This is an open-label, multicenter Phase 1 study to evaluate safety, tolerability and preliminary efficacy of oral LY3410738 in patients with isocitrate dehydrogenase 1 (IDH1) arginine 132 (R132)-mutant advanced solid tumors, including but not limited to cholangiocarcinoma, chondrosarcoma, and glioma or isocitrate dehydrogenase 2 (IDH2) arginine 140 (R140) or arginine 172 (R172) mutant cholangi…

NCT04567420 — DNA-guided Second Line Adjuvant Therapy for High Residual Risk, Estrogen Receptor Positive, HER-2 Negative Breast Cancer (DARE)

StatusActive, not recruiting
PhasePhase 2
SponsorCriterium, Inc.
Enrollment70
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions; ;

A randomized, Phase II trial of circulating tumor DNA-guided second line Adjuvant therapy for high Residual risk, Estrogen Receptor positive, HER-2 negative breast cancer (DARE)

NCT05038735 — Study to Assess the Efficacy and Safety of Alpelisib Plus Fulvestrant in Participants With HR-positive (HR+), HER2-negative, Advanced Breast Cancer After Treatment With a CDK4/6 Inhibitor and an Aromatase Inhibitor.

StatusActive, not recruiting
PhasePhase 3
SponsorNovartis Pharmaceuticals
Enrollment210
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions; ;

The purpose of this study is to complement Study CBYL719C2301 (SOLAR-1) and obtain more comprehensive data on the efficacy and safety of alpelisib (BYL719) in combination with fulvestrant compared with placebo plus fulvestrant in men or postmenopausal women with HR-positive, HER2-negative advanced breast cancer with a PIK3CA mutation who progressed or relapsed on or after treatment with an AI p…

NCT05703178 — Web-based Pain Coping Skills Training for Breast Cancer Survivors With AI-Associated Arthralgia

StatusActive, not recruiting
PhasePhase 3
SponsorNorthwestern University
Enrollment452
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; Arthralgia; Pain, Chronic
Interventions;

The main goal of this clinical trial is to test benefits of completing online pain coping skills training program in women who have been diagnosed with stage I-III breast cancer, who have completed their primary cancer treatment, who are taking an AI medication, and who have arthralgia. Arthralgia is a type of joint, bone, and muscle pain that is a common side effect of AI medications. The main…

NCT05607004 — (Z)-Endoxifen for the Treatment of Premenopausal Women With ER+/HER2- Breast Cancer

StatusActive, not recruiting
PhasePhase 2
SponsorAtossa Therapeutics, Inc.
Enrollment87
Study TypeINTERVENTIONAL
ConditionsBreast Neoplasms; Invasive Breast Cancer; Estrogen-receptor-positive Breast Cancer; HER2-negative Breast Cancer
Interventions;

This open-label research study is studying (Z)-endoxifen as a possible treatment for pre-menopausal women with ER+/HER2- breast cancer. (Z)-endoxifen belongs to a group of drugs called selective estrogen receptor modulators or “SERM”, which help block estrogen from attaching to cancer cells. This study has two parts: a pharmacokinetic part and a treatment part.

The PK part (how the body proces…

Not Yet Recruiting

NCT07676383 — Precision Navigation to Improve Community Cancer Screening Participation

StatusNot yet recruiting
PhaseN/A
SponsorHunan Cancer Hospital
Enrollment1500
Study TypeINTERVENTIONAL
ConditionsCancer Screening; Lung Cancer; Breast Cancer; Colorectal Cancer; Upper Gastrointestinal Cancer
Interventions;

This study will evaluate whether a precision navigation intervention can help community residents at high risk for cancer complete recommended cancer screening. The study will be conducted in communities participating in an urban cancer screening program in China.

Eligible participants will be adults aged 45 to 74 years who are permanent residents of participating communities and have been ide…

NCT06983691 — Patient Navigation for HER2+ Metastatic Breast Cancer Patients Treated With Tucatinib

StatusNot yet recruiting
PhaseN/A
SponsorDuke University
Enrollment26
Study TypeINTERVENTIONAL
ConditionsHER2+ Metastatic Breast Cancer (MBC)
Interventions

The goal of this study is to test a novel nurse-delivered patient navigation program for women with HER2+ metastatic breast cancer (mBC) receiving tucatinib, trastuzumab, and capecitabine. The program will focus on enhancing understanding of the treatment regimen, managing symptoms and adherence, and improving coping and self-management skills. If successful, the program could be integrated int…

NCT07619534 — Collection of CSF Samples From Participants With Metastatic Triple Negative Breast Cancer (TNBC) and HER2+ Breast Cancer With no Prior History Nor Active Radiographically Detectable Brain Metastases

StatusNot yet recruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment139
Study TypeOBSERVATIONAL
ConditionsBreast Cancer; Breast Carcinoma; Cancer of the Breast; Malignant Neoplasm of Breast
Interventions

Background:

Breast cancer is the most common cancer among women. It can often spread to the liver, lungs, bones, or brain. Breast cancer that spreads to the brain is often fatal. Researchers want to know if tumor DNA found in spinal fluid, blood, or tumor tissue can help predict when the cancer will spread to the brain. They want to collect these fluid and tissue samples for research.

Objecti…

NCT07689929 — Research on AI Models for Predicting Breast Cancer Treatment Effectiveness to Guide Her-2 Targeted ADC Therapy

StatusNot yet recruiting
PhaseN/A
SponsorZhejiang Cancer Hospital
Enrollment900
Study TypeOBSERVATIONAL
ConditionsBreast Cancer

This study aims to develop an AI-based predictive tool to help clinicians more accurately determine whether breast cancer patients can benefit from HER-2-targeted antibody-drug conjugate (T-DXd) therapy before treatment. While HER-2-targeted ADC drugs have significantly improved outcomes for patients with HER-2 positive and low-expression advanced breast cancer, there are notable individual dif…

NCT07619365 — Trastuzumab Deruxtecan and Lovastatin in HER2-low and Ultralow Advanced or Metastatic Breast Cancer

StatusNot yet recruiting
PhasePhase 2
SponsorWashington University School of Medicine
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; Advanced Breast Cancer; Metastatic Breast Cancer
Interventions;

The purpose of this study is to evaluate use of lovastatin, a drug that may lower CAV-1 levels, in order to increase HER2 expression on cells and enhance the uptake and efficacy of trastuzumab deruxtecan (T-DXd) in HER2-low and ultralow advanced metastatic breast cancer. Trastuzumab deruxtecan (T-DXd) is an FDA approved antibody drug conjugate for HER2-low and ultralow breast cancer and lovasta…

NCT07690852 — Environmental Exposure Assessment in High-Risk and Early-Onset Breast Cancer Care

StatusNot yet recruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment423
Study TypeOBSERVATIONAL
ConditionsBreast Carcinoma
Interventions

This study evaluates patient and provider attitudes about environmental exposure risk assessments into clinical care for female patients at average or high risk for breast cancer and/or diagnosed with early onset breast cancer.

NCT07689721 — ctDNA-Guided Intraventricular Therapy for CNS Malignancies

StatusNot yet recruiting
PhaseN/A
SponsorAlireza Mansouri
Enrollment77
Study TypeINTERVENTIONAL
ConditionsLeptomeningeal Disease; Glioblastoma; Brain Metastases; Non-Small Cell Lung Cancer; Breast Cancer
Interventions

This prospective, single-center study will evaluate whether cerebrospinal fluid (CSF) circulating tumor DNA (ctDNA) testing using the Belay Summit assay can improve the clinical management of patients with malignant gliomas or brain metastases from non-small cell lung cancer (NSCLC) or breast cancer who are suspected of having central nervous system (CNS) disease. Patients undergoing clinically…

Enrolling by Invitation

NCT07328516 — Natural History Study of Early Life Exposures in Agriculture (ELEA)

StatusEnrolling by invitation
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment64277
Study TypeOBSERVATIONAL
ConditionsProstate Cancer; Leukemia; Breast Cancer; Melanoma; Colorectal Cancer

Study Description:

ELEA is an observational cohort study that will collect exposure information and biospecimens from the adult children of the Agricultural Health Study (AHS) cohort (https://aghealth.nih.gov/about; Protocol OH93NCN013).

The primary hypothesis is that early life exposures, particularly those found in the agricultural environment, are associated with cancer and other adverse h…

Completed Trials

NCT00006421 — Breast Imaging Studies in Women at High Genetic Risk of Breast Cancer: Annual Follow-Up Study

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment200
Study TypeOBSERVATIONAL
ConditionsBreast Cancer
Interventions

This study will explore new screening methods for early detection of breast and ovarian cancer in women at high risk for these diseases, because they have an altered breast cancer 1 (BRCA1) or breast cancer 2 (BRCA2) gene. It will also try to determine if breast tissue characteristics in women with a BRCA1 or BRCA2 mutation differ from those in women with a normal gene.

Premenopausal women bet…

NCT00040222 — Clinical, Genetic, Behavioral, Laboratory and Epidemiologic Characterization of Individuals and Families at High Risk of Breast/Ovarian Cancer

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment377
Study TypeOBSERVATIONAL
ConditionsFamilial Ovarian Cancer; Familial Breast Cancer; BRCA1-associate Malignancies; BRCA2-associated Malignancies

Individuals and families with known or suspected syndromes that include breast, ovarian or genetically-related cancers are enrolled in this family study, which is a syndrome-specific sub-set of the long-standing DCEG Human Genetics Program umbrella family studies protocol (78-C-0039). Cancer outcomes are documented through review of medical, vital, and pathology records. Selected individuals an…

NCT00475761 — Breast Mammogram and Tissue Study

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment466
Study TypeOBSERVATIONAL
ConditionsBreast Neoplasms

Background:

Women whose mammograms show a lot of dense areas are more likely to develop breast cancer and to have cancers that are missed by mammograms.

It is unclear why some factors lead to having dense breasts and why having dense breasts increases the risk of developing breast cancer.

Objectives:

To determine why some women s breasts look dense on mammograms.

To determine what types of…

NCT03671330 — Efficacy and Safety of Ribociclib in Pre- and Postmenopausal Chinese Women With HR Positive, HER2-negative, Advanced Breast Cancer.

StatusCompleted
PhasePhase 2
SponsorNovartis Pharmaceuticals
Enrollment327
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions; ;

This was a randomized, double-blind, placebo-controlled study conducted in Chinese women with hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-) advanced breast cancer, plus an open-label, single-arm pharmacokinetic (PK) subset in postmenopausal Chinese women with HR+, HER2- advanced breast cancer.

NCT05365230 — A Randomized Trial Evaluating Personalized vs Guideline-based Well Follow-up Strategies for Patients With Early-stage Breast Cancer

StatusCompleted
PhasePhase 4
SponsorOttawa Hospital Research Institute
Enrollment261
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions;

After breast cancer patients complete the acute phase of their treatment (i.e. surgery, chemotherapy and/or radiation therapy), they are routinely followed in clinic every 3-6 months for several years. Multiple guideline recommendations exist with no consensus on the optimal follow-up schedule due to lack of randomized data to support any particular follow-up recommendation. Therefore the inves…

NCT07691294 — Endoscopic Assisted Latissimus Dorsi Musculocutaneous Flap for Breast Reconstruction

StatusCompleted
PhaseN/A
SponsorKasr El Aini Hospital
Enrollment15
Study TypeINTERVENTIONAL
ConditionsAcquired Breast Deformity; Breast Cancer; Post Burn Breast Deformities
Interventions

This prospective single-arm case series evaluates the feasibility, safety, and clinical outcomes of endoscopic-assisted latissimus dorsi musculocutaneous flap harvest for breast reconstruction. The study includes women with post-oncologic or post-burn breast deformities requiring autologous tissue reconstruction with a skin paddle measuring 6 cm or less in its greatest dimension.

The primary o…

NCT05565534 — Diabetes Care for Breast Cancer Patients

StatusCompleted
PhaseN/A
SponsorWeill Medical College of Cornell University
Enrollment74
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; PreDiabetes; Type 2 Diabetes
Interventions

The goal of this study is to find a new way to make diabetes care better for patients with breast cancer and diabetes who are currently receiving cancer treatment. We will have two groups, the researchers will decide who is in which group. One group will be working with a nurse who is trained in diabetes care while the other does not. This will allow the investigators to see if having a trained…

NCT06115902 — A Study of TQB2102 for Injection in Patients With Recurrent/Metastatic Breast Cancer

StatusCompleted
PhasePhase 1
SponsorChia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.
Enrollment153
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions

TQB2102 is an antibody-drug conjugate comprised of a humanised antibody against Human Epidermal Growth Factor Receptor 2 (HER2), an enzyme-cleavable linker, and a topoisomerase I inhibitor payload, which combine the ability of antibodies to specifically target tumour cells with the highly potent killing activity of drugs with payloads too toxic for systemic administration. This is a Phase 1/Pha…

StatusCompleted
PhaseN/A
SponsorAstraZeneca
Enrollment22
Study TypeOBSERVATIONAL
ConditionsUnresectable Breast Cancer; Metastatic Breast Cancer; HER2-low Expressing Breast Cancer; HER2-positive Breast Cancer
Interventions

Trastuzumab deruxtecan (T-DXd) has been studied in multiple global prospective DESTINY-Breast trials and has a marketing authorization from Health Canada for patients with HER2-positive metastatic breast cancer (mBC) and HER2-low mBC, respectively.

Multiple stakeholders, including clinicians, patients, regulators, and healthcare decision makers, are interested in real-world treatment-related o…

NCT06636591 — Pilot Study of Neoadjuvant Chemotherapy Combined With Immunotherapy and Multimodal Thermal Therapy for HER2-negative Breast Cancer

StatusCompleted
PhaseN/A
SponsorFudan University
Enrollment14
Study TypeINTERVENTIONAL
ConditionsBreast Cancer Female; HER2-negative Breast Cancer
Interventions;

In this study, breast cancer (BC) patients eligible for inclusion will be divided into two groups according to molecular typing and subtyping, which combined immunotherapy and multimodal thermal therapy with conventional neoadjuvant chemotherapy, to explore methods of immune induction for BC, enhance the efficacy of immunotherapy, and accumulate data for subsequent stages of clinical study.

NCT07689253 — Does Anesthesia Technique Impact on the Long-term Outcome 5 and 10 Years After the First Intervention in Primary Breast Cancer Surgery? A Follow-up Analysis.

StatusCompleted
PhaseN/A
SponsorUniversity of Zurich
Enrollment161
Study TypeOBSERVATIONAL
ConditionsBreast Cancer Females; Circulating Tumor Cells.Breast; Follow Up Analysis

Goal of this observational study is to analyze data about cancer recurrence rates 5 and 10 years after primary breast cancer surgery with propofol or sevoflurane anesthesia. Only patients who were enrolled in the primary interventional trial can participate.

NCT06529120 — Adaptation and Pilot Testing of a Mindfulness-Based Insomnia and Symptom Management Intervention for Women With Breast Cancer Receiving Treatment in Rural Medically Underserved Areas

StatusCompleted
PhaseN/A
SponsorDuke University
Enrollment15
Study TypeINTERVENTIONAL
ConditionsBreast Cancer
Interventions

Women with breast cancer often experience multiple difficult symptoms, for example insomnia, fatigue, stress, and pain. This study is being done to test a mindfulness-based insomnia and symptom management intervention for women with breast cancer (Nite2Day). Participants will complete six, 45-60 minute intervention sessions with a study therapist. Intervention sessions will be conducted remotel…

Other (Terminated)

NCT04251533 — Study Assessing the Efficacy and Safety of Alpelisib + Nab-paclitaxel in Subjects With Advanced TNBC Who Carry Either a PIK3CA Mutation or Have PTEN Loss

StatusTerminated
PhasePhase 3
SponsorNovartis Pharmaceuticals
Enrollment137
Study TypeINTERVENTIONAL
ConditionsTriple Negative Breast Neoplasms
Interventions; ;

The purpose of this study was to determine whether treatment with alpelisib in combination with nab-paclitaxel is safe and effective in subjects with advanced triple negative breast cancer (aTNBC) who carry either a PIK3CA mutation (Study Part A) or have PTEN loss (Study Part B1) or PTEN loss without PIK3CA mutation (Study Part B2)