Adenocarcinoma of the Prostate Clinical Trial
Official title:
A Compassionate Use Trial With Bicalutamide (Casodex) 150-mg for Subjects With Prostate Cancer
NCT number | NCT00636259 |
Other study ID # | 7054US/0014 |
Secondary ID | D6874L00006 |
Status | No longer available |
Phase | N/A |
First received | March 7, 2008 |
Last updated | June 10, 2008 |
Verified date | June 2008 |
Source | AstraZeneca |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Expanded Access |
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.
Status | No longer available |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Male |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with adenocarcinoma of the prostate - Subjects with locally advanced, and/or metastatic prostate cancer for whom surgical castration or other medical interventions are not considered appropriate or acceptable Exclusion Criteria: - Any known history of abnormal liver function tests - Any severe concomitant condition that would make it undesirable, in the clinician's opinion, for the subject to participate in the trial. - Known hypersensitivity to bicalutamide or any of the components found in bicalutamide |
N/A
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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AstraZeneca |
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