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Spots Global Cancer Trial Database for A Phase II Study of E7389 in Patients With Breast Cancer, Previously Treated With Anthracycline, Taxane and Capecitabine

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Trial Identification

Brief Title: A Phase II Study of E7389 in Patients With Breast Cancer, Previously Treated With Anthracycline, Taxane and Capecitabine

Official Title: A Phase II Open Label Single-Arm Study of E7389 in Patients With Locally Advanced or Metastatic Breast Cancer, Previously Treated With Anthracycline, Taxane, and Capecitabine Therapy, Refractory to the Last Prior Therapy for Their Disease

Study ID: NCT00246090

Conditions

Breast Cancer

Interventions

E7389

Study Description

Brief Summary: The purpose of this study is to evaluate the efficacy and safety of E7389 in Patients with locally advanced or metastatic breast cancer, previously treated with anthracycline, taxane, and capecitabine as prior therapy, and who are refractory to the last prior therapy for their disease.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Birmingham Hematology and Oncology, Birmingham, Alabama, United States

Birmingham Hematology and Oncology, Birmingham, Alabama, United States

Mercy Cancer Center, Hot Springs, Arkansas, United States

Arkansas Cancer Research Center, Little Rock, Arkansas, United States

Wilshire Oncology Medical Group, Inc., La Verne, California, United States

Rocky Mountain Cancer Center-Midtown, Denver, Colorado, United States

Rocky Mountain Cancer Center-Rose, Denver, Colorado, United States

Rocky Mountain Cancer Center, Littleton, Colorado, United States

Cancer Research Network, Plantation, Florida, United States

Hematology-Oncology Associates, Port Saint-Lucie, Florida, United States

Dr. Elizabeth Tan-Chiu, PA, Tamarac, Florida, United States

Peachtree Hematology And Oncology Consultants, Atlanta, Georgia, United States

University of Chicago, Chicago, Illinois, United States

Decatur Memorial Hospital, Decatur, Illinois, United States

Cancer Care and Hematology Specialist of Chicagoland, Niles, Illinois, United States

Central Indiana Cancer Center, Indianapolis, Indiana, United States

Monroe Medical Center, Munster, Indiana, United States

Northern Indiana Cancer Research Consortium, South Bend, Indiana, United States

University of Kansas Medical Center, Kansas City, Kansas, United States

Frederick Memorial Hospital, Regional Cancer Therapy Center, Frederick, Maryland, United States

Park Nicollet Institute, Minneapolis, Minnesota, United States

Missouri Cancer Associates, Columbia, Missouri, United States

Montana Cancer Specialists, Missoula, Montana, United States

Comprehensive Cancer Centers of Nevada, Henderson, Nevada, United States

New York Oncology Hematology, P.C, Albany, New York, United States

North Shore Hematology Oncology Associates, East Setakuet, New York, United States

Huntington Medical Group, PC, Huntington Station, New York, United States

Weill Cornell Breast Cancer Center, New York, New York, United States

SUNY Upstate Medical University, Syracuse, New York, United States

Northwestern Carolina Oncology And Hematology, PA, Hudson, North Carolina, United States

Raleigh Hematology Oncology Associates, Raleigh, North Carolina, United States

'Signal Point Hematology/Oncology, Inc., Middletown, Ohio, United States

Medical University of Ohio, Toledo, Ohio, United States

Cancer Care Associates, Oklahoma City, Oklahoma, United States

Cancer Care Associates, Oklahoma City, Oklahoma, United States

Cancer Care Associates, Tulsa, Oklahoma, United States

Willamette Valley Cancer Center, Eugene, Oregon, United States

Northwest Cancer Specialist Rose Qtr, Portland, Oregon, United States

Kaiser Permanente, Central Interstate Clinic, Hematology Oncology, Portland, Oregon, United States

Northwest Cancer Specialist Hoyt, Portland, Oregon, United States

Charleston Hematology Oncology, Charleston, South Carolina, United States

University of Tennessee Medical Center, Knoxville, Tennessee, United States

Harrington Cancer Center, Amarillo, Texas, United States

Texas Oncology, P.A. Bedford, Bedford, Texas, United States

Center For Oncology Research and Treatment, PA, Dallas, Texas, United States

Texas Oncology PA, Dallas, Texas, United States

Sammons Cancer Center-Dallas, Dallas, Texas, United States

El Paso Cancer Treatment Center West, El Paso, Texas, United States

El Paso Cancer Treatment Center, El Paso, Texas, United States

Texas Oncology PA, Houston, Texas, United States

Baylor College of Medicine, Breast Cancer Clinic, Houston, Texas, United States

North Texas Regional Cancer Center, Plano, Texas, United States

Tyler Cancer Center, Tyler, Texas, United States

Valley Oncology PA, Weslaco, Texas, United States

Utah Cancer Specialists, Salt Lake City, Utah, United States

Fairfax Northern VA Hematology Oncology PC, Fairfax, Virginia, United States

Oncology and Hematology Associates, Salem, Virginia, United States

Cancer Care Northwest, Spokane, Washington, United States

Northwest Cancer Specialist, Vancouver, Washington, United States

Yakima Valley Memorial Hospital, Yakima, Washington, United States

Hamilton Health Sciences Juravinski Cancer Centre, Hamilton, Ontario, Canada

NW Ontario Regional Cancer Centre, Thunder Bay, Ontario, Canada

Toronto East General Hospital, Toronto, Ontario, Canada

Centre Hospitaliere Universitaire de Montreal, Montreal, Quebec, Canada

McGill University, Dept. of Oncology, Clinical Research Program, Montreal, Quebec, Canada

Contact Details

Name: Dale Shuster, Ph.D.

Affiliation: Eisai Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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