A Study of IMC-A12 or Ramucirumab Plus Mitoxantrone and Prednisone in Prostate Cancer

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Eli Lilly and Company
ClinicalTrials.gov Identifier:
NCT00683475
First received: May 19, 2008
Last updated: May 16, 2014
Last verified: May 2014
  Purpose

The purpose of this study is to determine whether IMC-A12 or IMC-1121B (ramucirumab) with Mitoxantrone and Prednisone is effective in the treatment of metastatic androgen- independent prostate cancer (APIC).


Condition Intervention Phase
Prostate Cancer
Biological: IMC-A12
Drug: Mitoxantrone
Drug: Prednisone
Biological: IMC-1121B (ramucirumab)
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Phase 2, Multicenter, Randomized Study of IMC-A12 or IMC-1121B Plus Mitoxantrone and Prednisone in Metastatic Androgen-Independent Prostate Cancer (AIPC) Following Disease Progression on Docetaxel-Based Chemotherapy

Resource links provided by NLM:


Further study details as provided by Eli Lilly and Company:

Primary Outcome Measures:
  • Composite Progression-free Survival (cPFS) [ Time Frame: Randomization to composite progressive disease, up to 23.4 months ] [ Designated as safety issue: No ]

    Defined as the median time from randomization to the earliest of:

    1. Tumor progression by Response Evaluation Criteria in Solid Tumors (RECIST);
    2. Evidence of progression by bone scan, performed after completion of the first 3 cycles, demonstrating the appearance of >=2 new lesions;
    3. New skeletal events (New pathologic bone fracture in the region of metastatic disease; New bone lesion requiring radiation or surgery; Spinal cord or nerve root compression)
    4. Symptomatic progression (for participants without measurable disease);
    5. Other clinical events attributable to prostate cancer that require major interventions; or
    6. Death from any cause

    Participants who were ongoing with no progression or who discontinued treatment for reasons other than progression were censored at date of last assessment. Participants who started new anticancer treatment before progression were censored at date of last assessment before start of new anti-cancer therapy.



Secondary Outcome Measures:
  • Summary Listing of Participants Reporting Treatment-Emergent Adverse Events [ Time Frame: Randomization to 36.3 months ] [ Designated as safety issue: Yes ]
    Data presented are the number of participants who experienced A12 or 1121B (ramucirumab) related treatment-emergent adverse events (TEAE), treatment related serious adverse events (SAE), or any Grade 3 or higher TEAE; any TEAE leading to discontinuation of A12 or 1121B (ramucirumab) treatment, and any TEAE leading to dose modification of A12 or 1121B (ramucirumab). A summary of SAEs and other nonserious AEs, regardless of causality, is located in the Reported Adverse Event section.

  • Time to Radiographic Evidence of Disease Progression [ Time Frame: Randomization to date of radiographic progression, up to 36.3 months ] [ Designated as safety issue: No ]

    Time between date of randomization and earliest date of radiographic progression defined as either:

    1. Tumor progression by RECIST;
    2. Evidence of progression by bone scan;
    3. New skeletal events (New pathologic bone fracture in the region of metastatic disease; New bone lesion requiring radiation or surgery; Spinal cord or nerve root compression).

    Participants who were ongoing with no radiographic evidence of disease progression, who discontinued treatment for reasons other than progression,or died before progression were censored at date of last tumor or bone radiographic assessment. Participants who started a new anticancer treatment before progression were censored at date of last tumor or bone radiographic assessment before start of new anti-cancer therapy.


  • Prostate Specific Antigen (PSA) Response Rate [ Time Frame: Baseline up to data cut-off date (up to 36.3 months) ] [ Designated as safety issue: No ]
    PSA response rate is defined as the percentage of participants with a decrease in PSA >= 50 percent from baseline.

  • Composite Progression-free Survival (cPFS) at 6-months [ Time Frame: 6 months ] [ Designated as safety issue: No ]

    Data presented are the percentage of participants without disease progression at 6 months.

    Participants who were ongoing with no progression or who discontinued treatment for reasons other than progression were censored at date of last assessment. Participants who started new anticancer treatment before progression were censored at date of last assessment before start of new anti-cancer therapy.


  • Composite Progression-free Survival (cPFS) at 9-months [ Time Frame: 9 months ] [ Designated as safety issue: No ]

    Data presented are the percentage of participants without disease progression at 9 months.

    Participants who were ongoing with no progression or who discontinued treatment for reasons other than progression were censored at date of last assessment. Participants who started new anticancer treatment before progression were censored at date of last assessment before start of new anti-cancer therapy.


  • Composite Progression-free Survival (cPFS) at 12-months [ Time Frame: 12 months ] [ Designated as safety issue: No ]

    Data presented are the percentage of participants without disease progression at 12 months.

    Participants who were ongoing with no progression or who discontinued treatment for reasons other than progression were censored at date of last assessment. Participants who started new anticancer treatment before progression were censored at date of last assessment before start of new anti-cancer therapy.


  • Overall Survival (OS) [ Time Frame: First dose to death due to any cause up to 36.3 months ] [ Designated as safety issue: No ]
    Overall survival is defined as the time from randomization to the date of death due to any cause. Participants who were alive at the time of study completion were censored at the time the participant was last known to be alive.

  • Objective Response Rate (ORR) [ Time Frame: Baseline to date of progressive disease or death up to 36.3 months ] [ Designated as safety issue: No ]

    Objective response is Complete Response (CR) + Partial Response (PR), as classified by the investigators according to the Response Evaluation Criteria In Solid Tumors (RECIST) guidelines. CR is a disappearance of all target and non-target lesions; PR is at least a 30% decrease in the sum of the longest diameter of target lesions without new lesions and progression of non-target lesions.

    Objective response rate is calculated as a total number of participants with CR or PR divided by the total number of participants with measurable disease, multiplied by 100.


  • Maximum Concentration (Cmax) at Study Day 1 [ Time Frame: Day 1 ] [ Designated as safety issue: No ]

    Maximum Concentration (Cmax) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.


  • Maximum Concentration (Cmax) at Study Day 15 [ Time Frame: Day 15 ] [ Designated as safety issue: No ]

    Maximum concentration (Cmax) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.


  • Maximum Concentration (Cmax) at Study Day 16 [ Time Frame: Day 16 ] [ Designated as safety issue: No ]

    Maximum concentration (Cmax) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.


  • Maximum Concentration (Cmax) at Study Day 30 [ Time Frame: Day 30 ] [ Designated as safety issue: No ]

    Maximum concentration (Cmax) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.


  • Minimum Concentration (Cmin) at Study Day 1 [ Time Frame: Day 1 ] [ Designated as safety issue: No ]

    Minimum concentration (Cmin) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.


  • Minimum Concentration (Cmin) at Study Day 15 [ Time Frame: Day 15 ] [ Designated as safety issue: No ]

    Minimum concentration (Cmin) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.


  • Minimum Concentration (Cmin) at Study Day 16 [ Time Frame: Day 16 ] [ Designated as safety issue: No ]

    Minimum concentration (Cmin) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.


  • Minimum Concentration (Cmin) at Study Day 30 [ Time Frame: Day 30 ] [ Designated as safety issue: No ]

    Minimum concentration (Cmin) of Ramucirumab.

    All samples were assayed 36 months post sample collection, which exceeds the established long-term serum stability period for ramucirumab. Therefore, concentration data were invalid and pharmacokinetic (PK) analyses could not be conducted.



Enrollment: 132
Study Start Date: August 2008
Study Completion Date: September 2011
Primary Completion Date: September 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: IMC-1121B (ramucirumab) + Mitoxantrone + Prednisone Drug: Mitoxantrone
Mitoxantrone is to be administered as an I.V. infusion, at 12 milligrams/square meter (mg/m^2) over 5-15 minutes on Day 1 during a 3-week (21-day) cycle. Mitoxantrone treatment is to be continued for a maximum of 12 cycles (total cumulative dose of mitoxantrone is restricted to ≤ 144 mg/m^2) or until there is evidence of disease progression, death, or intolerable toxicity.
Drug: Prednisone
Prednisone (5 mg) is to be self-administered PO BID, each day of the 21-day cycle.
Biological: IMC-1121B (ramucirumab)
IMC-1121B (ramucirumab) is to be administered as an intravenous (IV) infusion, 6 milligrams/kilogram (mg/kg) over 1 hour on Days 1, 8, and 15 of each 3-week (21-day) cycle. Ramucirumab treatment is to continue until there is evidence of disease progression, death, intolerable toxicity, or other withdrawal criteria are met.
Other Names:
  • ramucirumab
  • IMC-1121B
  • LY3009806
Experimental: IMC-A12 + Mitoxantrone + Prednisone Biological: IMC-A12
IMC-A12 is to be administered as an I.V. infusion, 6 mg/kg over 1 hour on Days 1, 8, and 15 of each 3-week (21-day) cycle. IMC-A12 treatment is to continue until there is evidence of disease progression, death, intolerable toxicity, or other withdrawal criteria are met.
Other Names:
  • cixutumumab
  • LY3012217
Drug: Mitoxantrone
Mitoxantrone is to be administered as an I.V. infusion, at 12 milligrams/square meter (mg/m^2) over 5-15 minutes on Day 1 during a 3-week (21-day) cycle. Mitoxantrone treatment is to be continued for a maximum of 12 cycles (total cumulative dose of mitoxantrone is restricted to ≤ 144 mg/m^2) or until there is evidence of disease progression, death, or intolerable toxicity.
Drug: Prednisone
Prednisone (5 mg) is to be self-administered PO BID, each day of the 21-day cycle.

Detailed Description:

Prostate cancer is the most frequently diagnosed cancer in men and the second leading cause of cancer-related death in men in the United States. Chemotherapy, either as a single agent or in combination, may lead to clinical response, pain control, and/or improved quality of life. Docetaxel is now the first-line standard therapy for AIPC. Mitoxantrone was approved in 1996 for use in combination with corticosteroids as initial chemotherapy for pain related to advanced Hormone Refractory Prostate Cancer (HRPC). Hormonal manipulations and docetaxel-based chemotherapy are often effective in metastatic prostate cancer; however, disease becomes refractory to these interventions in the majority of men. Although mitoxantrone continues to be a significant agent in the treatment of HRPC, there exists a need for more efficacious therapy in docetaxel-refractory- AIPC. Because of the potential contribution of Insulin Like Growth Factor Receptor (IGF-IR) and VEGFR-2 mediated pathways in prostate cancer pathogenesis, it is hypothesized that each of these biological agents in combination with mitoxantrone and prednisone will result in clinically meaningful activity in AIPC. Therefore, ImClone plans to conduct a randomized Phase 2 trial to assess the safety and efficacy of IMC-A12 or IMC-1121B (ramucirumab) in combination with mitoxantrone and prednisone in participants with AIPC.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • The participant has histologically-confirmed adenocarcinoma of the prostate
  • The participant has radiographic evidence of metastatic prostate cancer (stage M1 or D2)
  • The participant has prostate cancer unresponsive or refractory to hormone therapy (androgen-independent)
  • The participant has had disease progression (clinical or radiographic) while receiving docetaxel, or within 120 days of receiving docetaxel-based chemotherapy and in the opinion of the investigator is unlikely to derive significant benefit from additional docetaxel-based therapy, or was intolerant to therapy with this agent
  • The participant must have evidence of progressive disease defined as at least one of the following;

    1. Progressive measurable disease: using conventional solid tumor criteria
    2. Bone scan progression: at least two new lesions on bone scan
    3. Increasing PSA: at least two consecutive rising PSA values over a reference value (PSA #1) taken at least 1 week apart. 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
  • The participant has a PSA ≥ 2 ng/mL
  • The participant has prior surgical or medical castration with a serum testosterone of <50 ng/mL. If the method of castration is luteinizing hormone releasing level hormone (LHRH) agonists, the participant must be willing to continue the use of LHRH agonists during protocol treatment
  • The participant has an Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2
  • The participant has adequate hematologic function (absolute neutrophil count [ANC]≥1500/uL, hemoglobin ≥9 g/dL, and platelets ≥100,000/uL)
  • The participant has adequate hepatic function (bilirubin ≤ 1.5 times the upper limit of normal (ULN), Aspartate Transaminase (AST) and Alanine Transaminase (ALT) ≤ 3 times the ULN, or ≤ 5 times the ULN if liver metastases are present)
  • The participant has adequate renal function (creatinine ≤ 1.5 x ULN or calculated creatinine clearance > 40 mL/min)
  • The participant's urinary protein is ≤ 1+ on dipstick or routine urinalysis (UA). If urine dipstick or routine analysis indicates ≥ 2+ proteinuria, then a 24-hour urine must be collected and must demonstrate < 1000 mg of protein in 24 hours to allow participation in the study
  • The participant has adequate coagulation function (an international normalized ratio [INR] ≤ 1.5 and a Partial Thromboplastin Time [PTT] ≤ 5 seconds above the ULN [unless on oral anticoagulant therapy]). Participants receiving full-dose anticoagulation therapy are eligible provided they meet all other criteria, are on a stable dose of oral anticoagulant or low molecular weight heparin (and if on warfarin have a therapeutic INR between 2 and 3)
  • The participant has a fasting serum glucose level of < 160 mg/dL, or below the ULN

Exclusion Criteria:

  • The participant has received more than one prior cytotoxic chemotherapy regimen for metastatic disease. (Participants who have had a treatment break followed by a second docetaxel-based regimen with subsequent disease progression are eligible.)
  • The participant has received prior therapy with mitoxantrone for advanced prostate cancer (prior adjuvant therapy with mitoxantrone is permitted)
  • The participant has a history of symptomatic congestive heart failure or has a pre-study echocardiogram or multigated acquisition (MUGA) scan with left ventricular ejection fraction (LVEF) that is ≥ 10% below the LLN
  • The participant has received radiotherapy ≤ 21 days prior to first dose of IMC-A12 or Ramucirumab
  • The participant is receiving corticosteroids (dexamethasone, prednisone, or others) at a dose > 5 mg prednisone orally (PO) two times per day (BID) or equivalent. Participants receiving corticosteroids at higher doses may be eligible if their corticosteroid therapy is tapered to study levels (prednisone 5 mg PO BID) prior to first dose of study medication, without concomitant clinical deterioration
  • The participant has known or suspected brain or leptomeningeal metastases
  • The participant has uncontrolled or poorly controlled hypertension
  • The participant has poorly controlled diabetes mellitus. Inclusion Criteria:
  • The participant has histologically-confirmed adenocarcinoma of the prostate
  • The participant has radiographic evidence of metastatic prostate cancer (stage M1 or D2)
  • The participant has prostate cancer unresponsive or refractory to hormone therapy (androgen-independent)
  • The participant has had disease progression (clinical or radiographic) while receiving docetaxel, or within 120 days of receiving docetaxel-based chemotherapy and in the opinion of the investigator is unlikely to derive significant benefit from additional docetaxel-based therapy, or was intolerant to therapy with this agent
  • The participant must have evidence of progressive disease defined as at least one of the following;

    1. Progressive measurable disease: using conventional solid tumor criteria
    2. Bone scan progression: at least two new lesions on bone scan
    3. Increasing PSA: at least two consecutive rising PSA values over a reference value (PSA #1) taken at least 1 week apart. 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
  • The participant has a PSA ≥ 2 ng/mL
  • The participant has prior surgical or medical castration with a serum testosterone of <50 ng/mL. If the method of castration is luteinizing hormone releasing level hormone (LHRH) agonists, the participant must be willing to continue the use of LHRH agonists during protocol treatment
  • The participant has an Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2
  • The participant has adequate hematologic function (absolute neutrophil count [ANC]≥1500/uL, hemoglobin ≥9 g/dL, and platelets ≥100,000/uL)
  • The participant has adequate hepatic function (bilirubin ≤ 1.5 times the upper limit of normal (ULN), aspartate transaminase [AST] and alanine transaminase [ALT]≤ 3 times the ULN, or ≤ 5 times the ULN if liver metastases are present)
  • The participant has adequate renal function (creatinine ≤ 1.5 x ULN or calculated creatinine clearance > 40 mL/min)
  • The participant's urinary protein is ≤ 1+ on dipstick or routine urinalysis (UA). If urine dipstick or routine analysis indicates ≥ 2+ proteinuria, then a 24-hour urine must be collected and must demonstrate < 1000 mg of protein in 24 hours to allow participation in the study
  • The participant has adequate coagulation function (an international normalized ratio [INR] ≤ 1.5 and a partial thromboplastin time [PTT] ≤ 5 seconds above the ULN [unless on oral anticoagulant therapy]). Participants receiving full-dose anticoagulation therapy are eligible provided they meet all other criteria, are on a stable dose of oral anticoagulant or low molecular weight heparin (and if on warfarin have a therapeutic INR between 2 and 3)
  • The participant has a fasting serum glucose level of < 160 mg/dL, or below the ULN

Exclusion Criteria:

  • The participant has received more than one prior cytotoxic chemotherapy regimen for metastatic disease. (Participants who have had a treatment break followed by a second docetaxel-based regimen with subsequent disease progression are eligible.)
  • The participant has received prior therapy with mitoxantrone for advanced prostate cancer (prior adjuvant therapy with mitoxantrone is permitted)
  • The participant has a history of symptomatic congestive heart failure or has a pre-study echocardiogram or multigated acquisition (MUGA) scan with left ventricular ejection fraction (LVEF) that is ≥ 10% below the LLN
  • The participant has received radiotherapy ≤ 21 days prior to first dose of IMC-A12 or Ramucirumab
  • The participant is receiving corticosteroids (dexamethasone, prednisone, or others) at a dose > 5 mg prednisone orally (PO) two times per day (BID) or equivalent. Participants receiving corticosteroids at higher doses may be eligible if their corticosteroid therapy is tapered to study levels (prednisone 5 mg PO BID) prior to first dose of study medication, without concomitant clinical deterioration
  • The participant has known or suspected brain or leptomeningeal metastases
  • The participant has uncontrolled or poorly controlled hypertension
  • The participant has poorly controlled diabetes mellitus. Participants with a history of diabetes are allowed to participate, provided that their blood glucose is within normal range (fasting < 120 mg/dL or below ULN) and that they are on a stable dietary or therapeutic regimen for this condition
  • The participant has a known human immunodeficiency virus infection or acquired immunodeficiency syndrome-related illness with a history of diabetes are allowed to participate, provided that their blood glucose is within normal range (fasting < 120 mg/dL or below ULN) and that they are on a stable dietary or therapeutic regimen for this condition
  • The participant has a known human immunodeficiency virus infection or acquired immunodeficiency syndrome-related illness
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00683475

  Hide Study Locations
Locations
United States, California
ImClone Investigational Site
La Jolla, California, United States, 92093
United States, Connecticut
ImClone Investigational Site
New Haven, Connecticut, United States, 06520
United States, Florida
ImClone Investigational Site
Boca Raton, Florida, United States, 33486
ImClone Investigational Site
Port St. Lucie, Florida, United States, 34952
United States, Georgia
ImClone Investigational Site
Atlanta, Georgia, United States, 30318
United States, Illinois
ImClone Investigational Site
Chicago, Illinois, United States, 60611
ImClone Investigational Site
Chlcago, Illinois, United States, 60637
ImClone Investigational Site
Evanston, Illinois, United States, 60201
ImClone Investigational Site
Maryville, Illinois, United States, 62062
United States, Iowa
ImClone Investigational Site
Cedar Rapids, Iowa, United States, 52402
United States, Louisiana
ImClone Investigational Site
Metairie, Louisiana, United States, 70006
United States, Michigan
ImClone Investigational Site
Ann Arbor, Michigan, United States, 48109
United States, Minnesota
ImClone Investigational Site
Rochester, Minnesota, United States, 55905
United States, Missouri
ImClone Investigational Site
St Louis, Missouri, United States, 63110
United States, Montana
ImClone Investigational Site
Billings, Montana, United States, 59101
United States, New Jersey
ImClone Investigational Site
Roseland, New Jersey, United States, 07068
United States, New York
ImClone Investigational Site
Buffalo, New York, United States, 14263
ImClone Investigational Site
East Setauket, New York, United States, 11733
ImClone Investigational Site
New York, New York, United States, 10021
ImClone Investigational Site
New York, New York, United States, 10032
ImClone Investigational Site
New York, New York, United States, 10016
ImClone Investigational Site
New York, New York, United States, 10019
United States, North Carolina
ImClone Investigational Site
Durham, North Carolina, United States, 27710
United States, Ohio
ImClone Investigational Site
Cleveland, Ohio, United States, 44195
United States, Pennsylvania
ImClone Investigational Site
Philadelphia, Pennsylvania, United States, 19111
ImClone Investigational Site
Pittsburgh, Pennsylvania, United States, 15232
United States, South Carolina
ImClone Investigational Site
Greenville, South Carolina, United States, 29605
United States, Tennessee
ImClone Investigational Site
Knoxville, Tennessee, United States, 37920
ImClone Investigational Site
Nashville, Tennessee, United States, 37203
United States, Texas
ImClone Investigational Site
Abilene, Texas, United States, 79606
ImClone Investigational Site
Dallas, Texas, United States, 75246
ImClone Investigational Site
Houston, Texas, United States, 77030
ImClone Investigational Site
Houston, Texas, United States, 77030-4009
United States, Washington
ImClone Investigational Site
Seattle, Washington, United States, 98104
ImClone Investigational Site
Seattle, Washington, United States, 98109
United States, Wisconsin
ImClone Investigational Site
Madison, Wisconsin, United States, 53792
Sponsors and Collaborators
Eli Lilly and Company
Investigators
Study Director: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) Eli Lilly and Company
  More Information

No publications provided

Responsible Party: Eli Lilly and Company
ClinicalTrials.gov Identifier: NCT00683475     History of Changes
Other Study ID Numbers: 13924, CP18-0601, I4T-IE-JVBS
Study First Received: May 19, 2008
Results First Received: May 16, 2014
Last Updated: May 16, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Eli Lilly and Company:
Prostate Cancer

Additional relevant MeSH terms:
Prostatic Neoplasms
Genital Neoplasms, Male
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Genital Diseases, Male
Prostatic Diseases
Mitoxantrone
Prednisone
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Central Nervous System Agents
Glucocorticoids
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Antineoplastic Agents, Hormonal
Anti-Inflammatory Agents

ClinicalTrials.gov processed this record on July 29, 2014