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Number: 201012801 Principal Investigator: Cashen, Amanda
Title: A phase I dose escalation study of intravenous decitabine in combination with oral bexarotene in patients with Acute Myeloid Leukemia (AML)
Phase: I Disease Site: Myeloid and Monocytic Leukemia
Participating Site(s):
 
Main Campus
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South County
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West County
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Contact: 800-600-3606 or info@ccadmin.wustl.edu

Description:
The goal of this study is to determine the best dose of bexarotene in combination with decitabine in order to treat patients with Acute Myeloid Leukemia (AML) that has come back after chemotherapy or that is newly diagnosed.
 
More Information:
ClinicalTrials.gov Link
Internal Protocol Documents (requires Siteman administrative database password)