Trial Search Results

AMG 102 in Combination With Mitoxantrone and Prednisone in Subjects With Previously Treated Castrate Resistant Prostate Cancer

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)

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Amgen

Stanford Investigator(s):

Intervention(s):

  • Drug: AMG 102
  • Drug: AMG 102
  • Drug: Mitoxantrone
  • Drug: Placebo
  • Drug: Prednisone

Phase:

Phase 1/Phase 2

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.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

Male

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Denise Haas
6507361252
Not Recruiting