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Spots Global Cancer Trial Database for Tezacitabine With or Without 5-Fluorouracil (5-FU) for Advanced Esophageal Cancer or Gastric Cancer

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Trial Identification

Brief Title: Tezacitabine With or Without 5-Fluorouracil (5-FU) for Advanced Esophageal Cancer or Gastric Cancer

Official Title:

Study ID: NCT00054873

Study Description

Brief Summary: The purpose of this study is to evaluate the efficacy and safety of tezacitabine when given alone or in combination with 5-fluorouracil (5-FU) to subjects who have advanced esophageal or gastric adenocarcinoma.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

ACRC/Arizona Clinical Research Center, Tucson, Arizona, United States

Glendale Memorial Hospital, Glendale, California, United States

USC/Norris Comprehensive Cancer Center, Los Angeles, California, United States

Tower Hematology Oncology Medical Group, Los Angeles, California, United States

Comprehensive Cancer Center at DRMC, Palm Springs, California, United States

Desert Regional Medical Center, Palm Springs, California, United States

Sharp Clinical Oncology Research, San Diego, California, United States

UCSF Comprehensive Cancer Center, San Francisco, California, United States

Cancer Institute Medical Group, Santa Monica, California, United States

Denver VAMC, Denver, Colorado, United States

H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, United States

Memorial Regional Comprehensive Cancer Center, Weston, Florida, United States

Northwestern University, Feinberg School of Medicine, Division of Hematology/Oncology, Chicago, Illinois, United States

The University of Chicago, Chicago, Illinois, United States

Ochsner Clinic Foundation, New Orleans, Louisiana, United States

LSU Health Sciences Center, Dept. of Medicine, Hematology/Oncology, Shreveport, Louisiana, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

University of Michigan Medical Center, Ann Arbor, Michigan, United States

Josephine Ford Cancer Center, Henry Ford Health System, Detroit, Michigan, United States

Kansas City Oncology and Hematology Group, Kansas City, Missouri, United States

Washington University School of Medicine, St. Louis, Missouri, United States

Duke University Medical Center, Durham, North Carolina, United States

Cleveland Clinic Foundation, Cleveland, Ohio, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

The Sarah Cannon Cancer Center, Tennessee Oncology, Nashville, Tennessee, United States

Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, United States

University of Texas, MD Anderson Cancer Center, Houston, Texas, United States

Swedish Cancer Institute, Seattle, Washington, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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