Clinical Trials Directory

Trials / Completed

CompletedNCT00103701

BMS-354825 in Patients With Chronic Accelerated, or Blast Phase Chronic Myelogenous Leukemia or Philadelphia Positive Acute Lymphoblastic Leukemia

Phase I Study of BMS-354825 in Patients With Chronic Accelerated, or Blast Phase Chronic Myelogenous Leukemia or Philadelphia Positive Acute Lymphoblastic Leukemia

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
Sponsor
Bristol-Myers Squibb · Industry
Sex
All
Age
14 Years
Healthy volunteers
Not accepted

Summary

The purpose of this clinical research study is to understand the safety and efficacy of BMS-354825 in patients with chronic, accelerated, or blast phase chronic myelogenous leukemia (CML) or Philadelphia positive acute lymphoblastic leukemia (ALL) who are resistant to or intolerant of imatinib mesylate (Gleevec).

Conditions

Interventions

TypeNameDescription
DRUGDasatinibTablets, Oral, 15- 240 mg, Once or twice daily, 0-3 years depending on response.

Timeline

Start date
2003-11-01
Primary completion
2006-03-01
Completion
2006-03-01
First posted
2005-02-15
Last updated
2011-04-14

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00103701. Inclusion in this directory is not an endorsement.