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AMG 102 in Combination With Mitoxantrone and Prednisone in Subjects With Previously Treated Castrate Resistant Prostate Cancer
Not Recruiting
Trial ID: NCT00770848
Purpose
The primary objectives of this study are the following:
Phase 1b: To identify a safe dose level of AMG 102, up to 15 mg/kg Q3W, to combine with
mitoxantrone and prednisone (MP) Phase 2: To estimate with adequate precision the effect of
the addition of AMG 102 to MP, compared with placebo plus MP, as assessed by the hazard ratio
(HR) for overall survival (OS) of previously treated subjects with castrate-resistant
prostate cancer (CRPC)
Official Title
A Phase 1b/2 Study to Assess the Safety and Efficacy of AMG 102 in Combination With Mitoxantrone and Prednisone in Subjects With Previously Treated Castrate Resistant Prostate Cancer
Stanford Investigator(s)
Sandy Srinivas
Professor of Medicine (Oncology) and, by courtesy, of Urology
Eligibility
Inclusion Criteria:
- Pathologically confirmed adenocarcinoma of the prostate
- Radiographic evidence of metastatic disease
- Progressive disease meeting at least one of the following criteria:
1. a sequence of at least 2 rising PSA values measured at a minimum of 1 week apart
with a 2 ng/mL minimum starting value, or
2. progression according to RECIST criteria for measurable lesions, or
3. appearance of 2 or more new lesions on bone scan.
- History of prior taxane-based chemotherapy for metastatic prostate cancer
- For patients without a history of surgical castration, continued GnRH analog
administration is required
- ECOG Performance status of 0 or 1
- Life expectancy ≥ 3 months
Exclusion Criteria:
- Treatment with external beam radiotherapy ≤ 14 days before enrollment or
radiopharmaceutical ≤8 weeks
- ≤ 4 weeks since receipt of most recent prior chemotherapy, non-GnRH analog hormonal
therapy (except for continuing corticosteroids) or other systemic therapy to treat
prostate cancer and <6 weeks since receipt of prior bevacizumab.
- Known CNS metastases (epidural disease is allowed if it has been treated and there is
no progression in the treated area).
- Significant cardiovascular disease
- LVEF < 50% by MUGA or ECHO
- Treatment of infection with systemic anti-infectives within 7 days before enrollment
(with the exception of uncomplicated urinary tract infection)
- Concurrent or prior (within 7 days of enrollment) anticoagulation therapy, except that
use of low dose coumarin-type anticoagulants or heparins for prophylaxis against
central venous catheter thrombosis is allowed
- Major surgical procedure ≤30 days before enrollment or not yet recovered from prior
major surgery
- Presence of peripheral edema > Grade 2
- Known positive test for HIV, hepatitis C, chronic or active hepatitis B
- Serious or non-healing wound
- Unable to begin protocol specified treatment within 7 days after enrollment
- Other investigational procedures are excluded.
Intervention(s):
drug: AMG 102
drug: Mitoxantrone
drug: Placebo
drug: Prednisone
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Denise Haas
6507361252