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

Completed · Phase 1

Conditions studied: Leukemia, Myeloid, Chronic-phase, Leukemia, Lymphoblastic, Acute, Philadelphia-positive

In brief

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).

Key facts

Study ID

NCT00103701

Run by

Bristol-Myers Squibb

Starts

2003-11-01

Expected to finish

2006-03-01

Last updated by the study team

2011-04-14

Who can join

Age: 14 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with Philadelphia chromosome positive, chronic, accelerated or blast phase BML or ALL.
• Patients must have primary or acquired hematologic resistance to imatinib mesylate or have intolerance of imatinib mesylate.
• Men and women, 14 years of age or older.
• Adequate renal function.
• Adequate hepatic function.
• Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy throughout the study and for a period of at least 1 month before and at least 3 months after the study in such a manner that the risk of pregnancy is minimized.

You may not qualify if…

• Patients who are eligible and willing to undergo transplantation during the screening period.
• Women who are pregnant or breastfeeding.
• A serious uncontrolled medical disorder or active infection that would impair the ability of the subject to receive protocol therapy.
• Uncontrolled or significant cardiovascular disease.
• Medications that increase bleeding risk.
• Medications that change heart rhythms.
• Dementia or altered mental status that would prohibit the understanding of rendering of informed consent.
• History of significant bleeding disorder or unrelated to CML.
• Evidence of organ dysfunction or digestive dysfunction that would prevent administration of study therapy.
• Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for treatment of either a psychiatric or physical (e.g., infectious disease) illness must not be enrolled into this study.

Where it is running

• Local Institution — Los Angeles, California, United States
• Local Institution — Houston, Texas, United States

Full record on ClinicalTrials.gov

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