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YM598 in Patients With Rising PSA After Initial Therapy for Localized Prostate Cancer

Phase 2
Terminated
Conditions
Prostate Cancer
Registration Number
NCT00050297
Lead Sponsor
Astellas Pharma Inc
Brief Summary

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.

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 (21)

University Clinic AZ

🇧🇪

Brussels, Belgium

University Clinic UCL St. Luc

🇧🇪

Brussels, Belgium

Private Urology Out-patient Ward

🇨🇿

Jablonec nad Nisou, Czech Republic

Clinic of Urology, University Hospital

🇨🇿

Prague, Czech Republic

Hôpital Bichat, service de Urology

🇫🇷

Paris, France

Haingasse 22

🇩🇪

Bad Homburg, Germany

Klinik und Poliklinik für Urologie, Universitätsklinikum Carl-Gustav-Carus

🇩🇪

Dresden, Germany

Klinik u. Poliklinik für Urologie, Philipps Universität, Baldingerstraße

🇩🇪

Marburg, Germany

Krummbogen 15

🇩🇪

Marburg, Germany

Regional Hospital, Department of Urology

🇵🇱

Bydgoszcz, Poland

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University Clinic AZ
🇧🇪Brussels, Belgium

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