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NCT00050297 Clinical Trial

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

Prostate Cancer Clinical Trial

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00050297
Other study ID # 598-CL-004
Secondary ID
Status Terminated
Phase Phase 2
First received December 3, 2002
Last updated June 6, 2012
Est. completion date February 2004

Study information
Verified date June 2012
Source Astellas Pharma Inc
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Terminated
Enrollment 0
Est. completion date February 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• YM598

Locations
Country Name City State
Belgium University Clinic AZ Brussels
Belgium University Clinic UCL St. Luc Brussels
Czech Republic Private Urology Out-patient Ward Jablonec nad Nisou
Czech Republic Clinic of Urology, University Hospital Králové
Czech Republic Clinic of Urology, University Hospital Olomouc
Czech Republic Clinic of Urology, University Hospital Prague
France Hôpital Bichat, service de Urology Paris
Germany 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
Poland Regional Hospital, Department of Urology Bydgoszcz
Poland MedSource Poland Gdansk
Poland Bielanski Hospital, Department of Urology Warszawa
Poland Oncology Center, Department of Urinary Tract Cancer Warszawa
Poland Medical University, Clinic of Urology Wroclaw
Spain Complejo Hospitaliaro Juan Canalejo, Servicio de Urología Corunna
Spain Fundacion Hospital Alcorcón, Servicio Urología Madrid
Spain Hospital Universitario Principe de Asturias, Servicio de Urología, Ctra. Madrid
United Kingdom Department of Urology, Bristol Royal Infirmary Bristol
United Kingdom Department of Urology, Gartnavel Hospital Glasgow
United Kingdom Department of Urology, Norfolk & Norwich Hospital Norwich
United Kingdom Department of Urology, Taunton & Somerset Hospital Taunton

Sponsors (2)
Lead Sponsor Collaborator
Astellas Pharma Inc Astellas Pharma US, Inc.

Countries where clinical trial is conducted

Belgium,  Czech Republic,  France,  Germany,  Poland,  Spain,  United Kingdom, 

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