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Spots Global Cancer Trial Database for Bicalutamide (Casodex™) Versus Placebo in Patients With Early Prostate Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Bicalutamide (Casodex™) Versus Placebo in Patients With Early Prostate Cancer

Official Title: A Randomized Double-Blind Comparative Trial of Bicalutamide (Casodex™) Versus Placebo in Patients With Early Prostate Cancer.

Study ID: NCT00657904

Interventions

Bicalutamide
Placebo

Study Description

Brief Summary: The purpose of this trial is to study the effect - in terms of time to progression and overall survival - of 2 years of adjuvant bicalutamide 150mg monotherapy, versus placebo, in subjects with histologically or cytologically confirmed non-metastatic adenocarcinoma of the prostate gland.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Research Site, Birmingham, Alabama, United States

Research Site, Mobile, Alabama, United States

Research Site, Scottsdale, Arizona, United States

Research Site, Tucson, Arizona, United States

Research Site, Berkeley, California, United States

Research Site, Laguna Woods, California, United States

Research Site, Newport Beach, California, United States

Research Site, San Diego, California, United States

Research Site, San Francisco, California, United States

Research Site, Santa Monica, California, United States

Research Site, Thousand Oaks, California, United States

Research Site, Torrance, California, United States

Research Site, Van Nuys, California, United States

Research Site, Denver, Colorado, United States

Research Site, Middlebury, Connecticut, United States

Research Site, New Haven, Connecticut, United States

Research Site, Washington, District of Columbia, United States

Research Site, Aventura, Florida, United States

Research Site, Bay Pines, Florida, United States

Research Site, Boca Raton, Florida, United States

Research Site, Daytona Beach, Florida, United States

Research Site, Fort Myers, Florida, United States

Research Site, Gainesville, Florida, United States

Research Site, Miami, Florida, United States

Research Site, Ocala, Florida, United States

Research Site, St. Augustine, Florida, United States

Research Site, Atlanta, Georgia, United States

Research Site, Chicago, Illinois, United States

Research Site, Fort Wayne, Indiana, United States

Research Site, Greenwood, Indiana, United States

Research Site, Iowa City, Iowa, United States

Research Site, Kansas City, Kansas, United States

Research Site, Louisville, Kentucky, United States

Research Site, Shreveport, Louisiana, United States

Research Site, Greenbelt, Maryland, United States

Research Site, Rockville, Maryland, United States

Research Site, Burlington, Massachusetts, United States

Research Site, Newtown, Massachusetts, United States

Research Site, Ann Arbor, Michigan, United States

Research Site, Detroit, Michigan, United States

Research Site, Rochester, Minnesota, United States

Research Site, Hattiesburg, Mississippi, United States

Research Site, Jackson, Mississippi, United States

Research Site, St. Louis, Missouri, United States

Research Site, Omaha, Nebraska, United States

Research Site, Lebanon, New Hampshire, United States

Research Site, Albany, New York, United States

Research Site, Bronx, New York, United States

Research Site, Manhasset, New York, United States

Research Site, New York, New York, United States

Research Site, Rochester, New York, United States

Research Site, Syracuse, New York, United States

Research Site, Asheville, North Carolina, United States

Research Site, Durham, North Carolina, United States

Research Site, Raleigh, North Carolina, United States

Research Site, Cincinnati, Ohio, United States

Research Site, Portland, Oregon, United States

Research Site, Lancaster, Pennsylvania, United States

Research Site, Philadelphia, Pennsylvania, United States

Research Site, Cordova, Tennessee, United States

Research Site, Nashville, Tennessee, United States

Research Site, Dallas, Texas, United States

Research Site, Houston, Texas, United States

Research Site, San Antonio, Texas, United States

Research Site, Salt Lake City, Utah, United States

Research Site, Danville, Virginia, United States

Research Site, Richmond, Virginia, United States

Research Site, Virginia Beach, Virginia, United States

Research Site, Seattle, Washington, United States

Research Site, Madison, Wisconsin, United States

Research Site, Milwaukee, Wisconsin, United States

Research Site, Cheyenne, Wyoming, United States

Research Site, Calgary, Alberta, Canada

Research Site, Edmonton, Alberta, Canada

Research Site, Victoria, British Columbia, Canada

Research Site, Winnipeg, Manitoba, Canada

Research Site, Halifax, Nova Scotia, Canada

Research Site, Hamilton, Ontario, Canada

Research Site, Kingston, Ontario, Canada

Research Site, London, Ontario, Canada

Research Site, North York, Ontario, Canada

Research Site, Oakville, Ontario, Canada

Research Site, Toronto, Ontario, Canada

Research Site, Montreal, Quebec, Canada

Research Site, Quebec, , Canada

Contact Details

Name: William See

Affiliation: Medical College of Wisconsin

Role: PRINCIPAL_INVESTIGATOR

Name: David G. McLeod

Affiliation: Walter Reed Army Medical Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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