Study Using CP-461 to Treat Advanced Prostate Cancer | NCT00036075 | Trialant
CompletedInterventionalPhase 2Updated Oct 17, 2011
Study Using CP-461 to Treat Advanced Prostate Cancer
ClinicalTrials.gov ID
NCT00036075
Lead Sponsor
Astellas Pharma IncINDUSTRY
Overall Status
Completed
Study Type
Interventional
Phase
Phase 2
Enrollment
25
Last Update Posted
Oct 17, 2011Estimated
Start Date
Aug 2001
Completion Date
Dec 2005Actual
Brief Summary
The purpose of this study is to investigate whether an investigational drug, CP-461, is safe and effective for the treatment of patients with prostate cancer and who have measurable disease.
Prostate Cancer
CP-461
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Eligibility Criteria:
Male 18 years of age.
Histologically confirmed adenocarcinoma of the prostate, stage D1 or D2.
Failure of androgen ablation (orchiectomy or LHRH, flutamide).
Patients must have PSA progression and progression in measurable disease.
No prior history of systemic chemotherapy.
No investigational drugs within 4 weeks of study entry.
No radiation therapy or hormonal therapy within 4 weeks of study entry.
No isotope therapy within 6 weeks of study entry.
No antiandrogens within 4 weeks of study entry. Patients must continue LHRH.
If patients had prior surgery, it must be at least 21 days prior to study entry, and the patient must have recovered from all side effects.
Patients must have stopped bisphosphonates 28 days prior to study entry.
No prior malignancy allowed except for adequately treated basal cell or squamous cell skin cancer, or adequately treated stage I or II cancer from which the patient is currently in remission, and has been disease free for at least 5 years.
Patients must have recovered from major infections and/or surgical procedures, and in the opinion of the investigator not have significant active concurrent medical illness, such as a history of significant neurologic or psychiatric disorders including psychotic disorders, dementia, or seizures that would preclude protocol treatment or survival.
All patients must be informed of the investigational nature of the study and must sign and give written informed consent in accordance with institutional and federal guidelines.
No other chemotherapeutic, biological response modifiers, radiation therapy, corticosteroid therapy, or hormonal concomitant therapy (except continuation of LHRH) may be given during treatment. Patients should not be planning on receiving concomitant bisphosphonates.