Prostate Cancer Clinical Trial

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A Rollover Study for Patients Who Received Tremelimumab in Other Protocols, to Allow the Patients Access to Tremelimumab Until This Agent Becomes Commercially Available or Development is Discontinued.

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Summary

This study is intended to provide access to tremelimumab for patients who have previously received tremelimumab in a clinical trial.

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Eligibility Criteria

Inclusion Criteria:

The subject must have already received tremelimumab in another protocol
Females of childbearing potential must agree to practice a form of effective contraception for 12 months following any dose of study drug. The definition of effective contraception will be based on the judgement of the investigator.
Subject must be willing and able to provide written informed consent and to comply with scheduled visits and other trial procedures

Exclusion Criteria:

None

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

37

Study ID:

NCT00378482

Recruitment Status:

Completed

Sponsor:

AstraZeneca

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There are 6 Locations for this study

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Research Site
Los Angeles California, 90024, United States
Research Site
Tampa Florida, 33612, United States
Research Site
Ann Arbor Michigan, 48109, United States
Research Site
New York New York, 10016, United States
Research Site
Houston Texas, 77030, United States
Research Site
Newecastle Upon Tyne , NE7 7, United Kingdom
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How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

37

Study ID:

NCT00378482

Recruitment Status:

Completed

Sponsor:


AstraZeneca

How clear is this clinincal trial information?

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