Status:
COMPLETED
Study of Abarelix in Androgen-Independent Prostate Cancer Progressing After Agonist Therapy
Lead Sponsor:
PRAECIS Pharmaceuticals Inc.
Conditions:
Prostate Cancer
Eligibility:
MALE
18+ years
Phase:
PHASE2
Brief Summary
This is a Phase 2, open-label study in subjects with androgen-independent prostate cancer who have progressed following treatment with an LHRH agonist. Up to 22 subjects will be enrolled. Enrollment w...
Eligibility Criteria
Inclusion
- Signed informed consent
- Histologically or cytologically confirmed prostate cancer that has progressed within 60 days of the start of screening despite castrate levels of testosterone from treatment with an LHRH agonist. Progression will be defined as one or more of the following: \*A rising PSA, defined as at least two consecutive rises in PSA over a reference value (PSA #1). The first rising PSA (PSA #2) must be taken at least one week after PSA #1. A third PSA (PSA #3) is required to be greater than PSA #2; if not, a fourth PSA (PSA #4) is required to be greater than PSA #2, OR
- The appearance of new metastatic lesions on a bone scan, OR
- Progression of known lesions or the appearance of new metastatic lesions on CT, MRI, chest x-ray, or other radiographic evaluations.
- Subject whose hormonal therapy includes an anti-androgen must have the anti-androgen discontinued prior to the start of screening (at least 6 weeks for bicalutamide and at least 4 weeks otherwise). If there is a reduction in the PSA after anti-androgen withdrawal, the subject must continue to demonstrate progression as defined above after anti- androgen withdrawal to be eligible.
- ECOG Performance Status ≤ 3
- Age ≥ 18 years of age
- Life expectancy ≥ 6 months
- Serum testosterone less than or equal to 50 ng/dL
- PSA ≥ 5 ng/mL (if progression is determined from a rise in PSA)
- WBC greater than or equal to 3,000/mm3
- Hematocrit ≥ 30%
- Platelet count greater than or equal to 100,000/mm3
- Serum creatinine less than or equal to 2 x upper limit of normal (ULN)
- Bilirubin (direct or total) less than or equal to 2 x ULN
- SGPT (ALT) and SGOT (AST) less than or equal to 2 x ULN
Exclusion
- A subject is ineligible to participate in the study if he meets any of the following criteria:
- Prior treatment for prostate cancer with:
- Chemotherapy
- Radiopharmaceutical such as strontium or samarium
- Diethylstilbesterol or another estrogen agonist or antagonist
- Ketoconazole
- Aminoglutethimide
- Current treatment with Class IA (e.g., quinidine, procainamide) or Class III (e.g., amiodarone, sotalol) antiarrhythmic medication
- Currently taking PC SPES
- History of allergy to a LHRH agonist or GnRH antagonist
- Major surgery within 4 weeks
- Serious medical illnesses, including malnutrition, that in the judgment of the investigator would preclude protocol treatment
- Significant cardiovascular illness defined as NYHA class III or IV congestive heart failure or unstable angina within 6 months, myocardial infarction within 12 months, deep venous thrombosis within 2 years, or any history of acute pulmonary embolism
- Active second malignancy other than non-melanoma skin cancer or superficial bladder cancer
- Any uncontrolled infection, including HIV
- Any other experimental therapy within 4 weeks prior to study entry
- QTc \> 450 msec on a screening ECG obtained by the investigator
Key Trial Info
Start Date :
May 1 2004
Trial Type :
INTERVENTIONAL
End Date :
September 1 2005
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT00100243
Start Date
May 1 2004
End Date
September 1 2005
Last Update
September 19 2006
Active Locations (7)
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1
San Diego Center for Urology
La Mesa, California, United States, 91942
2
Southwest Florida Urological Associates
Fort Myers, Florida, United States, 33907
3
Panama City Urological Center
Panama City, Florida, United States, 32405
4
Columbus Urology Research, LLC
Columbus, Ohio, United States, 43214