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
| Type | Name | Description |
|---|---|---|
| DRUG | Dasatinib | Tablets, 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.