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Clinical Trial Summary

The primary purpose of this study is to determine the maximum tolerated dose and dose-limiting toxicities (DLTs) of weekly and every 3-weeks ABI-007 in combination with carboplatin (area under the curve [AUC]=6) in patients with ovarian cancer, primary peritoneal cancer, or fallopian tube cancer.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00407407
Study type Interventional
Source Celgene
Contact
Status Terminated
Phase Phase 1
Start date November 1, 2006
Completion date February 1, 2008

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