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| Name | Class |
|---|---|
| OSI Pharmaceuticals | INDUSTRY |
This is a study in which patients with prostate cancer treated by surgical removal of the prostate and considered to be at risk for prostate cancer recurrence will receive Exisulind 250 mg twice a day or placebo twice a day for two years.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Exisulind | Drug |
| Measure | Description | Time Frame |
|---|---|---|
| Assess efficacy of drug vs placebo regarding overall rate of biochemical progression | ||
| Assess the efficacy of drug vs placebo regarding time to biochemical progression | ||
| Assess efficacy of drug vs placebo regarding overall rate of clinical progression | ||
| Assess efficacy of drug vs placebo regarding time to clinical progression | ||
| Assess efficacy of drug vs placebo regarding cancer specific survival |
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Males 18 years of age or older with prostate cancer treated primarily by radical prostatectomy and randomized within 45 days after surgery may be eligible for enrollment into this protocol. Participants cannot have had hormonal therapy, cryotherapy, thermotherapy, or radiotherapy prior to entering the study.
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| Name | Affiliation | Role |
|---|---|---|
| Bradley C. Leibovich, M.D. | Mayo Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic | Rochester | Minnesota | 55905 | United States |
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| ID | Term |
|---|---|
| D011471 | Prostatic Neoplasms |
| ID | Term |
|---|---|
| D005834 | Genital Neoplasms, Male |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| C025463 | sulindac sulfone |
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| D005832 |
| Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D011469 | Prostatic Diseases |
| D052801 | Male Urogenital Diseases |