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YM598 Added to Mitoxantrone/Prednisone to Control Pain in Metastatic Prostate Cancer Patients No Longer Responding to Hormone Therapy

Phase 2
Terminated
Conditions
Hormone-Refractory Prostate Cancer
Prostatic Neoplasms
Registration Number
NCT00048659
Lead Sponsor
Astellas Pharma Inc
Brief Summary

The purpose of this study is to determine if patients who take YM598 in addition to mitoxantrone and prednisone (standard therapy) experience improvement in the pain associated with prostate cancer metastases in the bone.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (53)

Alaska Clinical Research Center, LLC

🇺🇸

Anchorage, Alaska, United States

San Bernardino Urological Associates

🇺🇸

San Bernardino, California, United States

Western Clinical Research, Inc.

🇺🇸

Torrance, California, United States

Shands Hospital

🇺🇸

Gainesville, Florida, United States

Sylvester Comprehensive Cancer Center

🇺🇸

Miami, Florida, United States

Georgia Urology,PA Research Institute

🇺🇸

Atlanta, Georgia, United States

University of Chicago, Section of Hematology/Oncology

🇺🇸

Chicago, Illinois, United States

University of Illinois, Department of Urology

🇺🇸

Chicago, Illinois, United States

Michiana Hematology/Oncology

🇺🇸

South Bend, Indiana, United States

The Urologic Institute of New Orleans

🇺🇸

Gretna, Louisiana, United States

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Alaska Clinical Research Center, LLC
🇺🇸Anchorage, Alaska, United States

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