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Clinical Trial Summary

This study is a multicenter, nonrandomized, open-label, dose-escalation with intra-patient dose-escalation, Phase 1 study of intravenous LY2523355 to determine the dose of LY2523355 that can be safely administered to participants with acute leukemia. Part A and Part B are dose escalation of two schedules in participants with acute leukemia. Parts A and B will enroll concurrently. Part C is a dose expansion for each schedule in participants with acute myeloblastic leukemia (AML).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01214655
Study type Interventional
Source Eli Lilly and Company
Contact
Status Terminated
Phase Phase 1
Start date June 2008
Completion date February 2011

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