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| Sponsor: | AstraZeneca |
|---|---|
| Information provided by: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT00636259 |
Purpose
This study provides compassionate use of bicalutamide (Casodex) at a 150-mg dose for subjects with prostate cancer prior to it becoming commercially available. The patient will receive bicalutamide 150-mg as long as the physician feels that the subject is benefiting from this therapy and safety information is provided regularly to AstraZeneca. Treatment will be discontinued after bicalutamide 150-mg becomes commercially available.
| Condition | Intervention |
|---|---|
|
Adenocarcinoma of the Prostate |
Drug: Bicalutamide (Casodex) |
| Study Type: | Expanded Access |
| Official Title: | A Compassionate Use Trial With Bicalutamide (Casodex) 150-mg for Subjects With Prostate Cancer |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | 7054US/0014, D6874L00006 |
| Study First Received: | March 7, 2008 |
| Last Updated: | June 10, 2008 |
| ClinicalTrials.gov Identifier: | NCT00636259 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
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Prostate cancer Casodex |
|
Neoplasms by Histologic Type Genital Neoplasms, Male Prostatic Diseases Antineoplastic Agents Hormone Antagonists Physiological Effects of Drugs Hormones, Hormone Substitutes, and Hormone Antagonists Urogenital Neoplasms Genital Diseases, Male Pharmacologic Actions |
Carcinoma Neoplasms Androgen Antagonists Neoplasms by Site Therapeutic Uses Bicalutamide Adenocarcinoma Prostatic Neoplasms Neoplasms, Glandular and Epithelial |