Prostate Cancer Clinical Trial

Safety and Tolerability Study of MDV3100 in Combination With Docetaxel in Men With Advanced Prostate Cancer

Summary

The purpose of this study is to determine the safety of MDV3100 given in combination with Docetaxel in men with advanced prostate cancer.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Willing and able to provide informed consent;
Men, 18 years of age or older;
Histologically or cytologically confirmed adenocarcinoma of the prostate;
Ongoing androgen deprivation therapy

Exclusion Criteria:

Severe concurrent disease;
Known or suspected brain metastasis;
History of another malignancy within the previous 5 years;
Prior treatment with docetaxel-based chemotherapy

Study is for people with:

Prostate Cancer

Phase:

Phase 1

Estimated Enrollment:

23

Study ID:

NCT01565928

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 2 Locations for this study

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Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States
Memorial Sloan-Kettering Cancer Center
New York New York, 10065, United States
Virginia Oncology Associates
Norfolk Virginia, 23502, United States

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 1

Estimated Enrollment:

23

Study ID:

NCT01565928

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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