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YM598 in Patients With Rising PSA After Initial Therapy for Localized Prostate Cancer
This study has been terminated.
Study NCT00050297   Information provided by Astellas Pharma Inc
First Received: December 3, 2002   Last Updated: March 31, 2006   History of Changes

December 3, 2002
March 31, 2006
 
 
 
 
Complete list of historical versions of study NCT00050297 on ClinicalTrials.gov Archive Site
 
 
 
YM598 in Patients With Rising PSA After Initial Therapy for Localized Prostate Cancer
 

The purpose of this study is to determine the optimal dosage of YM598 for slowing down disease progression in patients with rising PSA after initial therapy for localized prostate cancer.

 
Phase II
Interventional
Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Prostate Cancer
Drug: YM598
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Terminated
 
 
 
 
Male
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Belgium,   Czech Republic,   France,   Germany,   Poland,   Spain,   United Kingdom
 
NCT00050297
 
598-CL-004
Astellas Pharma Inc
Astellas Pharma US, Inc.
 
Astellas Pharma Inc
March 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP