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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00257478
Other study ID # 155-CL-007
Secondary ID
Status Completed
Phase Phase 2
First received November 22, 2005
Last updated June 6, 2012
Est. completion date March 2007

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

A study for the treatment of hormone refractory prostate cancer (HRPC) in patients previously treated with chemotherapy.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date March 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Histologically or cytologically confirmed prostate cancer.

- Prior chemotherapy regimen for prostate cancer

Exclusion Criteria:

- History of other malignancy in the last 5 years

- Major surgery within the past 21 days

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
YM155


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Astellas Pharma Inc Astellas Pharma US, Inc.

Countries where clinical trial is conducted

United States,  Netherlands,  United Kingdom, 

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