Prostate Cancer Clinical Trial

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An Open-Label Study of YM155 + Docetaxel in Subjects With Advanced Hormone Refractory Prostate Cancer and Other Solid Tumors

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Summary

To determine the feasibility and safety of administering YM155 in combination with docetaxel

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Full Description

This clinical trial is designed to include two parts:

Part 1: Assessment of feasibility and safety of administering YM155 in combination with docetaxel and prednisone in subjects with hormone refractory prostate cancer (HRPC) [ ENROLLMENT COMPLETED ]

Part 2: Assessment of feasibility and safety of administering YM155 in combination with docetaxel in subjects with solid tumors (except HRPC).

This registration has been updated to reflect the design requirements of PART 2.

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Eligibility Criteria

Inclusion Criteria:

Part 1:

Male subjects with histologically or cytologically confirmed adenocarcinoma of the prostate with clinical or radiological evidence of metastatic disease.

Part 2:

Subjects with histologically and cytologically confirmed solid tumors with measurable disease (except HRPC).

Exclusion Criteria:

Radiation therapy within 4 weeks of the start of study drug

Study is for people with:

Prostate Cancer

Phase:

Phase 1

Estimated Enrollment:

32

Study ID:

NCT00514267

Recruitment Status:

Completed

Sponsor:

Astellas Pharma Inc

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There is 1 Location for this study

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San Antonio Texas, 78229, United States

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Study is for people with:

Prostate Cancer

Phase:

Phase 1

Estimated Enrollment:

32

Study ID:

NCT00514267

Recruitment Status:

Completed

Sponsor:


Astellas Pharma Inc

How clear is this clinincal trial information?

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