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Clinical Trial Summary

To determine safety, tolerability and maximum tolerated dose of BMS-63233/XL413 in subjects with Refractory Hematologic Cancer


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00838890
Study type Interventional
Source Bristol-Myers Squibb
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date March 2009
Completion date January 2010

See also
  Status Clinical Trial Phase
Completed NCT03882203 - CLAGE Sequential With Flu-Bu Conditioning for Refractory Acute Leukemia Phase 2