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Spots Global Cancer Trial Database for Clinical Trial for Ovarian Cancer (OvaRex®)

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Trial Identification

Brief Title: Clinical Trial for Ovarian Cancer (OvaRex®)

Official Title: A Double-Blind, Placebo-Controlled, Multicenter Clinical Trial of Intravenous OvaRex® MAb-B43.13 as Post Chemotherapy Consolidation for Epithelial Carcinoma of Ovarian, Tubal or Peritoneal Origin

Study ID: NCT00050375

Conditions

Ovarian Cancer

Interventions

oregovomab

Study Description

Brief Summary: This study will compare the time to disease relapse between OvaRex® MAb-B43.13-treated patients and placebo-treated patients. This study will also compare assessments of survival, quality of life, immune response and safety between active and placebo groups.

Detailed Description: This a Phase III, double-blind, placebo-controlled, multi-center study of intravenous OvaRex® MAb-B43.13 as post-chemotherapy consolidation for epithelial carcinoma of ovarian, tubal, or peritoneal origin.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Comprehensive Cancer Institute, Huntsville, Alabama, United States

Western Regional Community Clinical Oncology Program, Phoenix, Arizona, United States

Little Rock Hematology Oncology Assoc., Little Rock, Arkansas, United States

St. Jude Medical Center, Fullerton, California, United States

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

Cedars-Sinai Medical Center, Los Angeles, California, United States

UCLA School of Medicine, Los Angeles, California, United States

Gynecologic Oncology Associates, Newport Beach, California, United States

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

Sharp Memorial Hospital, San Diego, California, United States

Stanford University, Stanford, California, United States

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

University of Connecticut Cancer Center, Farmington, Connecticut, United States

Northwestern Connecticut Oncology Hematology Associates, LLP, Torrington, Connecticut, United States

Florida Gynecologic Oncology, Fort Myers, Florida, United States

Florida Hospital Cancer Institute, Orlando, Florida, United States

Pensacola Research Consultants, Pensacola, Florida, United States

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

Medical College of Georgia, Augusta, Georgia, United States

The University of Chicago Hospitals, Chicago, Illinois, United States

St. Vincent Gynecologic Oncology, Indianapolis, Indiana, United States

Michiana Hematology Oncology PC, South Bend, Indiana, United States

Brown Cancer Center, Louisville, Kentucky, United States

Louisville Oncology, Louisville, Kentucky, United States

Lake Charles Medical Surgical Clinic, Lake Charles, Louisiana, United States

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

The Harry and Jeanette Weinberg Cancer Institute, Baltimore, Maryland, United States

New England Medical Center, Boston, Massachusetts, United States

Women's Specialty Center, Jackson, Mississippi, United States

Ellis Fischel Cancer Center, Columbia, Missouri, United States

Jersey Shore Medical Center, Neptune, New Jersey, United States

North Shore University Hospital, Manhasset, New York, United States

St. Vincent's Comprehensive Cancer Center, New York City, New York, United States

Nyack Hospital, Nyack, New York, United States

SUNY-HSC Syracuse, Crouse Hospital, Syracuse, New York, United States

Blumenthal Cancer Center, Charlotte, North Carolina, United States

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

University Hospital - Health Systems, Cleveland, Ohio, United States

GYN Oncology and Pelvic Surgery Associates, Columbus, Ohio, United States

ProMedica Health Systems, Toledo, Ohio, United States

Medical College of Ohio Cancer Institute, Toledo, Ohio, United States

Oklahoma University Health Sciences Center, Oklahoma City, Oklahoma, United States

Northwest Cancer Specialists-Northrup, Portland, Oregon, United States

Magee-Womens Hospital, Pittsburgh, Pennsylvania, United States

Brown University School of Medicine, Providence, Rhode Island, United States

South Carolina Oncology Associates, Columbia, South Carolina, United States

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

Chattanooga GYN Oncology, Chattanooga, Tennessee, United States

West Clinic, PC, Memphis, Tennessee, United States

Arlington Cancer Center, Arlington, Texas, United States

Southwest Regional Cancer Center, Austin, Texas, United States

Univ. of Texas SW Medical Center at Dallas, Dallas, Texas, United States

Texas Oncology, PA, Dallas, Texas, United States

Texas Oncology, Fort Worth, Texas, United States

The Center for Cancer and Blood Disorders, Fort Worth, Texas, United States

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

University of Virginia Cancer Center, Charlottesville, Virginia, United States

VA Oncology Associates, Norfolk, Virginia, United States

Carilion GYN Oncology Associates, Roanoke, Virginia, United States

Swedish Medical Center, Seattle, Washington, United States

Cancer Care Northwest, Spokane, Washington, United States

Northwest Cancer Specialists-Vancouver, Vancouver, Washington, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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