Prostate Cancer Clinical Trial

Continuation Trial Evaluating the Tolerability and Activity of FK228 in Patients That Completed Prior Study With FK228

Summary

The purpose of this study is to evaluate the safety and tolerability of extended treatment with FK228 in patients with metastatic renal cell carcinoma or hormone refractory prostate cancer who have at least demonstrated stable disease on prior Fujisawa sponsored FK228 clinical trials.

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Full Description

This is a Phase II, non-randomized, open-label, single arm, continuation trial.

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Eligibility Criteria

Inclusion Criteria:

Patient has completed 6 cycles of therapy in a prior Fujisawa-sponsored FK228 clinical trial;
Patient has immediate past participation (not to exceed 21 days from Day 15 of cycle 6 in the previous study) in a prior Fujisawa-sponsored FK228 clinical trial;
Patient has demonstrated stable disease, partial response or complete response as best overall response in their prior Fujisawa-sponsored FK228 clinical trial.

Exclusion Criteria:

Patient has been on a prior Fujisawa-sponsored FK228 clinical trial, left the trial and then received alternative anti-neoplastic therapy

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

2

Study ID:

NCT00106301

Recruitment Status:

Completed

Sponsor:

Celgene

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There are 5 Locations for this study

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City of Hope National Medical Center
Duarte California, 91010, United States
University of Florida
Gainesville Florida, 32610, United States
University of Chicago
Chicago Illinois, 60637, United States
Seattle Cancer Care Alliance
Seattle Washington, 98109, United States
Royal Marsden Hospital
Sutton , SM2 5, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

2

Study ID:

NCT00106301

Recruitment Status:

Completed

Sponsor:


Celgene

How clear is this clinincal trial information?

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