A Study of Oral Clofarabine in Adult Patients With Myelodysplastic Syndromes (MDS)

Exclusion Criteria

• •Have had a readjustment of dose and/or schedule of erythropoietin, granulocyte colony stimulating factor(G-CSF) or other growth factors within 8 weeks prior to the first dose of oral clofarabine.
• •Have had any other chemotherapy or any investigational therapy for MDS within 4 weeks of the first dose of oral clofarabine.
• •Have not recovered to ≤ Grade 2 in severity of any drug-related non-hematologic toxicity prior to the first dose of oral clofarabine.
• •Have an uncontrolled systemic fungal, bacterial, viral or other infection. Have a history of serious disease involving the heart.
• •Have a clinically significant cardiac assessment at screening or a known family history QT prolongation.
• •Currently uses a medication known to prolong the QT interval.
• •Have had any prior treatment with clofarabine (IV or oral).
• •Have had a diagnosis of another malignancy, unless the patient has been disease free for at least 3 years after completing curative intent therapy except for the following: a. Patients with treated non-melanoma skin cancer, in situ carcinoma, or cervical intraepithelial neoplasia, regardless of the disease-free duration, are eligible for this study if definitive treatment or the condition has been completed. b. Patients with organ-confined prostate cancer with no evidence of recurrent or progressive disease based on prostate specific antigen (PSA) values are also eligible for this study if hormonal therapy has been initiated or a radical prostatectomy has been performed.
• •Have prior positive test for the human immunodeficiency virus (HIV).
• •Have gastrointestinal disease or prior surgery, which may affect the ability of the patient to absorb oral clofarabine.
• •Is currently participating in another concurrent investigational protocol that is not restricted to data and/or sample collection for patient demographic and/or disease purposes.