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Spots Global Cancer Trial Database for Efficacy of Å6 in Ovarian Cancer Patients Following First-Line Chemotherapy and a Rising CA125 Levels

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Trial Identification

Brief Title: Efficacy of Å6 in Ovarian Cancer Patients Following First-Line Chemotherapy and a Rising CA125 Levels

Official Title: A Phase 2 Randomized, Double-Blind Trial of the Clinical Activity and Safety of Å6 in Patients With Asymptomatic CA125 Progression of Epithelial Ovarian Cancer After First-Line Chemotherapy

Study ID: NCT00083928

Study Description

Brief Summary: The purpose of this study is to determine whether injections of Å6 are effective in treating ovarian cancer patients who have completed first-line therapy and currently have no detectable cancer but have experienced a doubling of CA 125 levels.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

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

Desert Oasis Cancer Center, Casa Grande, Arizona, United States

California Oncology of the Central Valley, Fresno, California, United States

USC Keck School of Medicine Women's and Childrens Hospital, Los Angeles, California, United States

University of California Irvine Medical Center, Orange, California, United States

UC Davis Health System, Sacramento, California, United States

Scripps Cancer Center, San Diego, California, United States

University of Colorado Cancer Center, Aurora, Colorado, United States

Florida Hospital Cancer Institute, Orlando, Florida, United States

Medical College of Georgia Dept. of OB/GYN, St. Agusta, Georgia, United States

Tripler Army Medical Center, Honolulu, Hawaii, United States

Gynecologic Oncology, Hinsdale, Illinois, United States

St. Vincent Gyn-Onc, Indianapolis, Indiana, United States

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

University of Louisville JG Brown Cancer Center, Louisville, Kentucky, United States

Hematology & Oncology Specialists, New Orleans, Louisiana, United States

Barnes Jewish Hospital, St. Louis, Missouri, United States

Gabrail Cancer Center, Canton, Ohio, United States

OSU College of Medicine, Columbus, Ohio, United States

University of Oklahoma College of Medicine, Oklahoma City, Oklahoma, United States

Gynecologic-Oncology Research and Development, LLC, Greenville, South Carolina, United States

Chattanooga GYN Oncology, Chattanooga, Tennessee, United States

Brooke Army Medical Center, Fort Sam Houston, Texas, United States

Carilion Gynecologic Oncology Associates, Roanoke, Virginia, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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