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| Sponsors and Collaborators: |
Astellas Pharma Inc Astellas Pharma US, Inc. |
|---|---|
| Information provided by: | Astellas Pharma Inc |
| ClinicalTrials.gov Identifier: | NCT00048659 |
Purpose
The purpose of this study is to determine if patients who take YM598 in addition to mitoxantrone and prednisone (standard therapy) experience improvement in the pain associated with prostate cancer metastases in the bone.
| Condition | Intervention | Phase |
|---|---|---|
|
Hormone-Refractory Prostate Cancer Prostatic Neoplasms |
Drug: YM598 |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Contacts and Locations
Show 53 Study Locations
More Information
| Study ID Numbers: | 598-CL-008 |
| Study First Received: | November 4, 2002 |
| Last Updated: | March 31, 2006 |
| ClinicalTrials.gov Identifier: | NCT00048659 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
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Androgen-independent prostate cancer |
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Prednisone Prostatic Diseases Genital Neoplasms, Male Urogenital Neoplasms Pain |
Mitoxantrone Genital Diseases, Male Hormones Prostatic Neoplasms Androgens |
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Neoplasms Neoplasms by Site Prostatic Diseases Genital Neoplasms, Male |
Urogenital Neoplasms Genital Diseases, Male Prostatic Neoplasms |