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YM598 Added to Mitoxantrone/Prednisone to Control Pain in Metastatic Prostate Cancer Patients No Longer Responding to Hormone Therapy
This study has been terminated.
First Received: November 4, 2002   Last Updated: March 31, 2006   History of Changes
Sponsors and Collaborators: Astellas Pharma Inc
Astellas Pharma US, Inc.
Information provided by: Astellas Pharma Inc
ClinicalTrials.gov Identifier: NCT00048659
  Purpose

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.


Condition Intervention Phase
Hormone-Refractory Prostate Cancer
Prostatic Neoplasms
Drug: YM598
Phase II

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Resource links provided by NLM:

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00048659

  Show 53 Study Locations
Sponsors and Collaborators
Astellas Pharma Inc
Astellas Pharma US, Inc.
  More Information

No publications provided

Study ID Numbers: 598-CL-008
Study First Received: November 4, 2002
Last Updated: March 31, 2006
ClinicalTrials.gov Identifier: NCT00048659     History of Changes
Health Authority: United States: Food and Drug Administration

Keywords provided by Astellas Pharma Inc:
Androgen-independent prostate cancer

Study placed in the following topic categories:
Prednisone
Prostatic Diseases
Genital Neoplasms, Male
Urogenital Neoplasms
Pain
Mitoxantrone
Genital Diseases, Male
Hormones
Prostatic Neoplasms
Androgens

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Site
Prostatic Diseases
Genital Neoplasms, Male
Urogenital Neoplasms
Genital Diseases, Male
Prostatic Neoplasms

ClinicalTrials.gov processed this record on July 02, 2009