Breast Cancer Clinical Trial

A Study of Single-Agent Eribulin Mesylate as First-Line Therapy for Locally Recurrent or Metastatic Human Epidermal Growth Factor Receptor Two (HER2) Negative Breast Cancer

Summary

The purpose of this study is to assess the efficacy and safety of single-agent eribulin mesylate for first-line treatment of subjects with locally recurrent or metastatic breast cancer.

View Full Description

Full Description

This is a multicenter, single-arm, Phase 2 trial to assess the efficacy and safety of single-agent eribulin mesylate for first-line treatment of subjects with locally recurrent or metastatic human epidermal growth factor receptor (HER2)-negative breast cancer. A total of 52 adult female subjects will be enrolled and treated with eribulin mesylate (1.4 mg/m2 as an intravenous [i.v.] infusion over 2 to 5 minutes on Days 1 and 8 of each 3-week cycle).

View Eligibility Criteria

Eligibility Criteria

Key Inclusion Criteria

Females age 18 years or older at the time of informed consent

Have histologically or cytologically proven adenocarcinoma of the breast

Subjects with locally recurrent or metastatic disease with at least one measurable lesion according to Response Evaluation Criteria in Solid Tumors

(RECIST) criteria v 1.1

Human epidermal growth factor receptor (HER2)-negative disease as determined by fluorescence in situ hybridization (FISH) or 0 or 1+ by immunohistochemical (IHC) staining.

Life expectancy of greater than 24 weeks

Eastern Cooperative Oncology Group (ECOG) Performance Score (PS) of 0, 1 or 2

At least 12 months since prior neoadjuvant or adjuvant chemotherapy

At least 2 weeks since prior radiotherapy or endocrine therapy, with complete recovery from the effects of these interventions

Adequate renal function

Adequate bone marrow function

Adequate liver function

Key Exclusion Criteria

Subjects who meet any of the following criteria will be excluded from participation in this study:

Prior chemotherapy, biologic therapy, or investigational therapy for locally recurrent or metastatic breast cancer

Subjects who have had a prior malignancy other than carcinoma in situ of the cervix or nonmelanoma skin cancer

Prior exposure of greater than 360 mg/m2 doxorubicin or liposomal doxorubicin, greater than 120 mg/m2 mitoxantrone, greater than 90 mg/m2 idarubicin, or greater than720 mg/m2 epirubicin

Inflammatory breast cancer

Clinically significant cardiovascular impairment

Subjects with known CNS disease are not eligible, except for those with treated brain metastasis.

Pulmonary lymphangitic involvement that results in pulmonary dysfunction requiring the use of oxygen

Currently pregnant or breast-feeding.

Subjects with pre-existing Grade 3 or 4 neuropathy. Any peripheral neuropathy must recover to Grade 2 before enrollment.

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

56

Study ID:

NCT01268150

Recruitment Status:

Completed

Sponsor:

Eisai Inc.

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 17 Locations for this study

See Locations Near You

University of Miami
Miami Florida, 33136, United States
Augusta Oncology Associates
Augusta Georgia, 30901, United States
Central Georgia Cancer Care
Macon Georgia, 31088, United States
Northwest Georgia Oncology Centers, P.C.
Marietta Georgia, 30060, United States
Central Indiana Cancer Centers
Indianapolis Indiana, 46219, United States
Missouri Cancer Associates
Columbia Missouri, 65201, United States
Hematology Oncology Centers of Northern Rockies
Billings Montana, 59101, United States
New York Oncology Hematology, P.C.
Albany New York, 12206, United States
Weill Cornell Medical Center
New York New York, 10021, United States
Northwest Cancer Specialists, P.C.
Portland Oregon, 97225, United States
The West Clinic
Memphis Tennessee, 38120, United States
Texas Oncology- Bedford
Bedford Texas, 76022, United States
Texas Oncology - Medical City Dallas
Dallas Texas, 75230, United States
Texas Oncology-Dallas Presbyterian Hospital
Dallas Texas, 75231, United States
Cancer Care Centers of South Texas
San Antonio Texas, 78217, United States
Texas Oncology- Tyler
Tyler Texas, 75702, United States
Columbia Basin Hematology and Oncology
Kennewick Washington, 99336, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

56

Study ID:

NCT01268150

Recruitment Status:

Completed

Sponsor:


Eisai Inc.

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider