A Study for Patients With Acute Leukemia

Status Terminated

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

Clinical Trial Details

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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