ACTRN12606000372583
Active, not recruiting
Phase 2
A feasibility and efficacy study, evaluating the prostate specific antigen (PSA) response, of taxotere/prednisone in combination with thalidomide in hormone refractory prostate cancer
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Royal North Shore Hospital
- Enrollment
- 35
- Status
- Active, not recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Histologically/cytologically proven prostate adenocarcinoma2\. ALl patients are males, aged 18 years or more and must have prostate adenocarcinoma that is responsive or refractory to hormone therpay.3\. Prior treatment with crticosteroids is allowed.4\. life expectancy greater or equal to 3 months.5\. prior surgery is allowed. At least 4 weeks must have elapsed since the completion of surgery.6\. ECOG 0\-27\. Informed consent signed
Exclusion Criteria
- •1\. Prior cytotoxic chemotherapy (except monotherapy with estramustine)2\. prior isotope therapy3\. prior radiotherapy to \>25% of bone marrow (whole pelvic radiation is not allowed)4\. known brain leptomeningeal involvement.5\. Other malignancy6\. Uncontrolled medical condition7\. Prior Deep venous thrombosis or pulmonary embolism
Outcomes
Primary Outcomes
Not specified
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