Triple Negative Breast Cancer Clinical Trials
68 studies are recruiting for triple negative breast cancer in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies, page 3
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Evaluate BL-B01D1 in Patients With Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors
The objective of this study is to evaluate the safety, tolerability, and efficacy of BL-B01D1 in patients with Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Beverly Hills Cancer Center, Beverly Hills, California
- Locations
- 39 in total
- Run by
- SystImmune Inc.
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Neoadjuvant Therapy and Contrast-enhanced Mammography for Early Stage Breast Cancer
The purpose of this study is to compare a special type of mammogram that uses a contrast agent called contrast-enhanced digital mammography with contrast-enhanced digital breast tomosynthesis (CEDM+CEDBT), with breast magnetic resonance imaging imaging (MRI) for predicting the effect of neoadjuvant…
- Stage
- EARLY_Phase 1
- Ages
- 18 and older
- Site
- Stony Brook Breast Center, Stony Brook, New York
- Run by
- Alison Stopeck
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A Study of DR-0202 in Patients With Locally Advanced or Metastatic, Relapsed or Refractory Carcinomas
A phase 1a/1b, multicenter, open-label, dose escalation/expansion, multiple-dose study to evaluate the safety and activity of DR-0202 in patients with locally advanced or metastatic, relapsed or refractory carcinomas
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dren Investigational Site, Denver, Colorado
- Locations
- 10 in total
- Run by
- Dren Bio
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A Dose Escalation and Dose Expansion Study of Intratumoral ONM-501 Alone and in Combination With Cemiplimab in Patients With Advanced Solid Tumors and Lymphomas.
A phase 1, multicenter, open label, non-randomized dose escalation and dose expansion study to examine the maximum tolerated dose, (MTD), minimum effective dose (MED) and/or recommended dose for expansion (RDE) of intratumoral ONM-501 as monotherapy and in combination with a PD-1 checkpoint inhibit…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- St Vincent's Hospital, Darlinghurst, New South Wales
- Locations
- 16 in total
- Run by
- OncoNano Medicine, Inc.
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Sacituzumab Govitecan and Zimberelimab w/SRS in the Management of Metastatic Triple Negative Breast Cancer With Brain Metastases
This is a Phase I/II Study to determine the safety and efficacy of Sacituzumab Govitecan and Zimberelimab with stereotactic radiation (SRS) in participants with metastatic triple negative breast cancer with brain metastases, compared to treatment with Sacituzumab Govitecan alone.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Moffitt Cancer Center, Tampa, Florida
- Run by
- H. Lee Moffitt Cancer Center and Research Institute
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A Phase I/II Study of VLS-1488 in Subjects With Advanced Cancer
This is a first-in-human phase I/II study to examine the safety, tolerability and preliminary efficacy of VLS-1488 in subjects with advanced cancers.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Southern California, Los Angeles, California
- Locations
- 14 in total
- Run by
- Volastra Therapeutics, Inc.
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Lifestyle, Exercise, And Nutrition (LEAN) Trial on Pathologic Complete Response in TNBC
The purpose of this study is to examine whether a nutrition and exercise program can improve pathologic complete response (pCR) in women with triple-negative breast cancer (TNBC) receiving chemo-immunotherapy before surgery. Pathologic complete (pCR) response means that no cancer in the breast is s…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Yale University, New Haven, Connecticut
- Run by
- Yale University
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A Study to Evaluate the Safety and Efficacy of A2B395, an Allogeneic Logic-gated CAR T, in Participants With Solid Tumors That Express EGFR and Have Lost HLA-A*02 Expression
The goal of this study is to test A2B395, an allogeneic logic-gated Tmod™ CAR T-cell product in subjects with solid tumors including colorectal cancer (CRC), non-small cell lung cancer (NSCLC), head and neck squamous cell carcinoma (HNSCC), triple-negative breast cancer (TNBC), renal cell carcinoma…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Banner MD Anderson Cancer Center, Gilbert, Arizona
- Locations
- 10 in total
- Run by
- A2 Biotherapeutics Inc.
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A Phase 0 Multicenter Study of the Pharmacodynamic Effects of Intratumoral Microdose Administration of PBA-0111 in Patients With Solid Tumors
This is a multi-center, single arm, open-label, localized pharmacodynamic biomarker Phase 0 trial designed to study the biological effects within the tumor microenvironment of PBA-0111 when administered intratumorally in microdose quantities via the CIVO device.
- Stage
- EARLY_Phase 1
- Ages
- 18 and older
- Site
- LSU Health Sciences Center, Shreveport, Louisiana
- Run by
- Pure Biologics S.A.
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A Beta-only IL-2 ImmunoTherapY Study
This is a Phase 1/2, multi-center, open-label, dose-escalation and expansion study to evaluate safety and tolerability, PK, pharmacodynamic, and early signal of anti-tumor activity of MDNA11 alone or in combination with a checkpoint inhibitor in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sharp Memorial Hospital, San Diego, California
- Locations
- 27 in total
- Run by
- Medicenna Therapeutics, Inc.
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A Study to Evaluate the Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension in Triple Negative Breast Cancer Patients
The Nanosomal Docetaxel Lipid Suspension (NDLS) consists of uniformly sized micro particles of docetaxel suspended in a lipid based formulation. The advantage of such a Lipid Based formulation of Docetaxel is an improvement of the safety profile by eliminating excipients, polysorbate 80 and ethanol…
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Columbus Regional Research Institute, LLC, Columbus, Georgia
- Locations
- 4 in total
- Run by
- Jina Pharmaceuticals Inc.
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A Multicenter Cancer Biospecimen Collection Study
This study will collect de-identified tumor samples, with correlated clinical/demographic data and tissue histology, from patients selected or scheduled for pre-treatment tumor biopsy or who have had a recent pre-treatment tumor biopsy. These specimens and clinical data may be used in subsequent st…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Curebase, San Francisco, California
- Run by
- Cofactor Genomics, Inc.
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Correlation of Clinical Response to Pathologic Response in Patients With Early Breast Cancer
The purpose of this study is to learn whether clinical response (the amount a tumor shrinks based on imaging or tumor measurements obtained by physical exam) predicts pathologic response (the amount of tumor remaining when surgery is performed) in participants with breast cancer who are receiving c…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Harris Health System - Smith Clinic, Houston, Texas
- Locations
- 2 in total
- Run by
- Baylor Breast Care Center
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Phase 1a and Phase 2 Study for Safety, Preliminary Efficacy, PK and PD of ST-067
This is a multiphase, multicenter study, which includes a Phase 1a open-label, dose escalation monotherapy study of ST-067 given as an SC injection with or without obinutuzumab [Gazyva®] pre-treatment, by IV infusion, and in combination with pembrolizumab. A Phase 2 monotherapy arm is also planned;…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HonorHealth Research Institute, Scottsdale, Arizona
- Locations
- 6 in total
- Run by
- Simcha IL-18, Inc.
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Study of CRX100 as Monotherapy and in Combination With Pembrolizumab in Patients With Advanced Solid Malignancies
This clinical study is an open-label, Phase 1, dose-escalation study to determine the safety, tolerability, and efficacy of the drug product produced by Administering CRX100 alone and in combination with Pembrolizumab in advanced solid malignancies. Patients will be screened and evaluated to determ…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- HonorHealth Research Institute, Scottsdale, Arizona
- Locations
- 3 in total
- Run by
- BioEclipse Therapeutics
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A First-in-human, Phase I, Open-label, Multicenter Study of NM1F(Anti-PVRIG) in Patients With Advanced Solid Tumors
A Phase 1 Study to Investigate the Safety, Tolerability, Pharmacokinetics/Pharmacodynamics, and Antitumor Activity of NM1F as Monotherapy and in Combination with Pembrolizumab in Subjects with Locally Advanced/Metastatic Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology, Dallas, Dallas, Texas
- Locations
- 2 in total
- Run by
- Hefei TG ImmunoPharma Co., Ltd.
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First in Human Phase 1 Study of AG01 Anti-Progranulin/GP88 Antibody in Advanced Solid Tumor Malignancies
This is a first in human phase 1 study of AG01 an anti-Progranulin/Glycoprotein88 (PGRN/GP88) antibody in patients with advanced solid tumors. AG01 is a recombinant monoclonal antibody expressed in a CHO production cell line. The antibody AG01 binds to human PGRN/GP88, expressed on cancer cells. Th…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, Maryland
- Run by
- A&G Pharmaceutical Inc.
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The Gut Microbiome and Immune Checkpoint Inhibitor Therapy in Solid Tumors
The microbiome has the potential to serve as a robust biomarker of clinical response to immunotherapy. Additionally, microbial manipulation, through diet, exercise, prebiotics, probiotics, or microbially-derived metabolites, may prove to be beneficial in promoting anti-tumor immune responses. Howev…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Baptist Health Clinical Research, Elizabethtown, Kentucky
- Run by
- VastBiome
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.