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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00048659
Registration number
NCT00048659
Ethics application status
Date submitted
4/11/2002
Date registered
6/11/2002
Date last updated
7/06/2012
Titles & IDs
Public title
YM598 Added to Mitoxantrone/Prednisone to Control Pain in Metastatic Prostate Cancer Patients No Longer Responding to Hormone Therapy
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Scientific title
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Secondary ID [1]
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598-CL-008
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Hormone-Refractory Prostate Cancer
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Prostatic Neoplasms
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Condition category
Condition code
Cancer
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Prostate
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Eligibility
Key inclusion criteria
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Stopped early
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Data analysis
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
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Date of last participant enrolment
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Actual
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Date of last data collection
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Actual
1/06/2004
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Sample size
Target
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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Department of Medical Oncology, The Canberra Hospital - Canberra
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Department of Medical Oncology, Concord Hospital Medical Centre - Concord
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Recruitment hospital [3]
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Division of Oncology Ward, Royal Brisbane Hospital - Herston
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Department of Clinical Oncology, Royal North Shore Hospital - St Leonards
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Cancer Care Centre, St. George Hospital - Sydney
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Department of Medical Oncology, Newcastle Mater Hospital - Waratah
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Southern Medical Day Care Centre - Wollongong
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Recruitment hospital [8]
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Queen Elizabeth Hospital, Clinical Hematology & Oncology - Woodville
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Recruitment postcode(s) [1]
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- Canberra
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- Concord
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Recruitment postcode(s) [3]
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- Herston
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- St Leonards
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- Sydney
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Recruitment postcode(s) [6]
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- Waratah
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Recruitment postcode(s) [7]
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- Wollongong
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Recruitment postcode(s) [8]
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- Woodville
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Recruitment outside Australia
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United States of America
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Alaska
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California
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Washington
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Bruxelles
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Lyon
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France
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Paris
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Madrid
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Valencia
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Devon
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Surrey
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West Sussex
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Astellas Pharma Inc
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Address
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Commercial sector/industry
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Name [1]
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Astellas Pharma US, Inc.
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Ethics approval
Ethics application status
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Summary
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.
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Trial website
https://clinicaltrials.gov/study/NCT00048659
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00048659
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