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Sponsors and Collaborators: |
Astellas Pharma Inc Astellas Pharma US, Inc. |
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Information provided by: | Astellas Pharma Inc |
ClinicalTrials.gov Identifier: | NCT00257478 |
A study for the treatment of hormone refractory prostate cancer (HRPC) in patients previously treated with chemotherapy.
Condition | Intervention | Phase |
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Prostate Cancer Cancer of Prostate Prostatic Cancer Cancer of the Prostate |
Drug: YM155 |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Arizona | |
Tuscon, Arizona, United States, 85724 | |
United States, California | |
Los Angeles, California, United States, 90033 | |
United States, Idaho | |
Coeur d'Alene, Idaho, United States, 83814 | |
United States, New York | |
New York, New York, United States, 10016 | |
Bronx, New York, United States, 10461 | |
United States, Pennsylvania | |
Philadelphia, Pennsylvania, United States, 19111 | |
United States, Texas | |
San Antonio, Texas, United States, 78229 | |
Netherlands | |
Amsterdam, Netherlands | |
United Kingdom, Surry | |
Sutton, Surry, United Kingdom, SM2 5Pt |
Study Director: | D. Buell, MD | Astellas Pharma US, Inc. |
Study ID Numbers: | 155-CL-007 |
Study First Received: | November 22, 2005 |
Last Updated: | May 9, 2007 |
ClinicalTrials.gov Identifier: | NCT00257478 |
Health Authority: | United States: Food and Drug Administration |
Treatment Efficacy Treatment Effectiveness Disease Management Treatment Safety |
Prostatic Diseases Genital Neoplasms, Male Urogenital Neoplasms Genital Diseases, Male Prostatic Neoplasms |
Neoplasms Neoplasms by Site |