Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Bristol-Myers Squibb
Age
14–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible 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 be 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.
Clareo Health | BMS-354825 in Patients With Chronic Accelerated, or Blast Phase Chronic Myelogenous Leukemia or Philadelphia Positive Acute Lymphoblastic Leukemia
