Breast Cancer Clinical Trials in Seattle, Washington
18 studies are recruiting for breast cancer in Seattle, Washington 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.
Search these by distance from you
Studies now recruiting
-
A Study of HER3-DXd in Subjects With Locally Advanced or Metastatic Solid Tumors
This is a proof-of-concept study designed to investigate HER3-DXd monotherapy in locally advanced unresectable or metastatic solid tumors. The study is enrolling cohorts of participants with melanoma [cutaneous/acral], squamous cell carcinomas of the head and neck (SCCHN), HER2-negative gastric can…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Fred Hutchinson Cancer Center, Seattle, Washington
- Locations
- 96 in total
- Run by
- Daiichi Sankyo
-
A Study to Learn About the Study Medicine Called PF-07248144 in Combination With Fulvestrant in People With HR-positive, HER2-negative Advanced or Metastatic Breast Cancer Who Progressed After a Prior Line of Treatment.
The purpose of this study is to learn about the safety and effects of the study medicine PF-07248144 when given along with fulvestrant for the possible treatment of HR-positive, HER2-negative advanced or metastatic breast cancer. HR-positive breast cancer cells have proteins on their surface called…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Harborview Medical Center, Seattle, Washington
- Locations
- 433 in total
- Run by
- Pfizer
-
Phase 3 Study of Gedatolisib as First-Line Treatment for Patients With HR-Positive, HER2-Negative Advanced Breast Cancer (VIKTORIA-2)
This is a Phase 3, open-label, randomized, clinical trial evaluating the efficacy and safety of gedatolisib and palbociclib plus endocrine therapy for the treatment of patients with locally advanced or metastatic HR+/HER2- advanced breast cancer.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Fred Hutchinson Cancer Center, Seattle, Washington
- Locations
- 239 in total
- Run by
- Celcuity Inc
-
A Study Evaluating the Efficacy and Safety of Inavolisib Plus CDK4/6 Inhibitor and Letrozole vs Placebo + CDK4/6i and Letrozole in Participants With Endocrine-Sensitive PIK3CA-Mutated, Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer
This study will evaluate the efficacy and safety of the combination of inavolisib plus a cyclin-dependent kinase 4 and 6 inhibitor (CDK4/6i) and letrozole versus placebo plus a CDK4/6i and letrozole in the first-line setting in participants with endocrine-sensitive PIK3CA-mutated hormone receptor-p…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Swedish Cancer Institute - Issaquah, Seattle, Washington
- Locations
- 242 in total
- Run by
- Hoffmann-La Roche
-
The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)
The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation. The Phase 1 portion of the study will assess the safety, toler…
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- University of Washington, Fred Hutchinson Cancer Center, Seattle, Washington
- Locations
- 76 in total
- Run by
- PMV Pharmaceuticals, Inc
-
An Investigational Study of BG-75202 Alone and in Combination With Other Therapeutic Agents in Adults With Advanced Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-75202 (KAT6A/B inhibitor) alone and in combination with other therapies in participants with breast cancer and other advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fred Hutchinson Cancer Research Center, Seattle, Washington
- Locations
- 32 in total
- Run by
- BeOne Medicines
-
A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of BMS-986507 Combinations in Adult Participants With Advanced Solid Tumors
The purpose of this study is to evaluate the safety, tolerability, drug levels, and preliminary efficacy of BMS-986507 combinations in adult participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Swedish Medical Center, Seattle, Washington
- Locations
- 65 in total
- Run by
- Bristol-Myers Squibb
-
Palazestrant in Combination With Ribociclib for the First-line Treatment of ER+/HER2- Advanced Breast Cancer
This phase 3 clinical trial compares the efficacy and safety of palazestrant with ribociclib to letrozole and ribociclib in women and men who have not received prior systemic anti-cancer treatment for advanced breast cancer.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Clinical Trial Site, Seattle, Washington
- Locations
- 200 in total
- Run by
- Olema Pharmaceuticals, Inc.
-
ARTIDIS Nanomechanical Generated Measurements for Early Breast Lesions
This prospective, blinded, single-arm study aims to test the performance of nanomechanical phenotype in predicting tumor type, tumor aggressiveness, and neoadjuvant treatment response compared to the gold standard of histopathological assessment. The study involves patients with suspicious breast l…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Washington, Seattle, Washington
- Locations
- 6 in total
- Run by
- ARTIDIS AG
-
A Study of Elacestrant Versus Standard Endocrine Therapy in Women and Men With ER+,HER2-, Early Breast Cancer With High Risk of Recurrence
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.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Virginia Mason Medical Center, Seattle, Washington
- Locations
- 567 in total
- Run by
- Stemline Therapeutics, Inc.
-
Evaluating the Addition of Adjuvant Chemotherapy to Ovarian Function Suppression Plus Endocrine Therapy in Premenopausal Patients With pN0-1, ER-Positive/HER2-Negative Breast Cancer and an Oncotype Recurrence Score Less Than or Equal to 25
This Phase III Trial will determine whether adjuvant chemotherapy (ACT) added to ovarian function suppression (OFS) plus endocrine therapy (ET) is superior to OFS plus ET in improving invasive breast cancer-free survival (IBCFS) among premenopausal, early- stage breast cancer (EBC) patients with es…
- Stage
- Phase 3
- Ages
- 18 to 60
- Site
- Virginia Mason Medical Center, Seattle, Washington
- Locations
- 1261 in total
- Run by
- NRG Oncology
-
A Study of Emiltatug Ledadotin (Emi-Le) in Participants With Solid Tumors
A Study of Emi-Le in Participants with Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fred Hutchinson Cancer Center, Seattle, Washington
- Locations
- 26 in total
- Run by
- Day One Biopharmaceuticals, Inc.
-
I-SPY TRIAL: Neoadjuvant and Personalized Adaptive Novel Agents to Treat Breast Cancer
The purpose of this study is to further advance the ability to practice personalized medicine by learning which new drug agents are most effective with which types of breast cancer tumors and by learning more about which early indicators of response (tumor analysis prior to surgery via magnetic res…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Swedish Cancer Institute, Seattle, Washington
- Locations
- 42 in total
- Run by
- QuantumLeap Healthcare Collaborative
-
Quantitative MRI Assessment of Breast Cancer Therapy Response
The goal of this observational study is to investigate and validate multi-parametric magnetic resonance imaging (MRI) modalities for assessment of breast cancer response to neoadjuvant chemotherapy in a multi-site and multi-MRI scanner platform setting. This study is conducted at Oregon Health \& S…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Washington, Seattle, Washington
- Locations
- 4 in total
- Run by
- Corewell Health East
-
A Study of PARG Inhibitor ETX-19477 in Patients With Advanced Solid Malignancies
This is a two-part, open-label, multicenter, dose escalation and dose expansion study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and anti- tumor activity of ETX-19477, a novel reversible small molecule inhibitor of PARG.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fred Hutchinson Cancer Center, Seattle, Washington
- Locations
- 14 in total
- Run by
- 858 Therapeutics, Inc.
-
A Study of CLSP-1025 in Adult Patients With Solid Tumors That Harbor the p53 R175H Mutation
Phase 1 dose escalation and expansion study of CLSP-1025, a first-in-class HLA-A*02:01 specific T cell engager (TCE) targeting solid tumors that harbor the p53 R175H mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fred Hutchinson Cancer Center, Seattle, Washington
- Locations
- 21 in total
- Run by
- Clasp Therapeutics, Inc.
-
SYNERGY-AI: Artificial Intelligence Based Precision Oncology Clinical Trial Matching and Registry
International registry for cancer patients evaluating the feasibility and clinical utility of an Artificial Intelligence-based precision oncology clinical trial matching tool, powered by a virtual tumor boards (VTB) program, and its clinical impact on pts with advanced cancer to facilitate clinical…
- Stage
- Not phased
- Ages
- Any age
- Site
- Massive Bio SYNERGY-AI site, Seattle, Washington
- Locations
- 68 in total
- Run by
- Massive Bio, Inc.
-
MammaPrint, BluePrint, and Full-genome Data Linked With Clinical Data to Evaluate New Gene EXpression Profiles
The FLEX Registry will be implemented to operate as a large-scale, population based, prospective registry. All patients with stage I to III breast cancer who receive MammaPrint® and BluePrint testing on a primary breast tumor are eligible for entry into the FLEX Registry, which is intended to enabl…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Swedish Cancer Institute, Seattle, Washington
- Locations
- 134 in total
- Run by
- Agendia
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.