Phase I Study Evaluating TXA127 in Low/Intermediate-1 Risk Myelodysplastic Syndrome and Thrombocytopenia

Exclusion Criteria

• •Currently receiving any treatment for MDS other than transfusions (last transfusion must be at least 4 weeks prior to treatment).
• •If granulocyte and/or erythropoetic growth factors are currently being received, there should be a 4-week washout prior to treatment, and they may not be used during the study period.
• •Concurrent active malignancy (other than controlled prostate cancer, in situ cervical cancer, or basal cell cancer of the skin)
• •Prior history of bone marrow transplantation
• •Unstable angina, uncontrolled congestive heart failure \[NYHA \> class II\], uncontrolled hypertension \[diastolic \> 100 mmHg\], uncontrolled cardiac arrhythmia, or recent (within 1 year) myocardial infarction, or a QTc interval value \>450ms.
• •Received Anti-Thymocyte Globuline (ATG) within 6 months of screening
• •Received hypomethylating agents, immunomodulating agents, histone deacetylase inhibitors, cyclosporine, or mycophenolate within 4 weeks of start of treatment
• •Received IL-11 (oprelvekin) within 4 weeks before screening
• •Have ever previously received rTPO, PEG-rHuMGDF, eltrombopag, or romiplostim
• •Less than 4 weeks since receipt of any investigational agent (not FDA approved, for any indication)
• •History of arterial thrombosis (e.g., stroke or transient ischemic attack) in the past year
• •History of venous thrombosis that currently requires anti-coagulation therapy
• •Female subjects who are pregnant or breastfeeding. Women of childbearing potential are required to have a positive HCG serum or urine pregnancy test performed 7 days prior to first study drug dose
• •Women of childbearing potential who are unwilling to use an adequate form of contraception during the course of the study.
• •Subjects with current alcohol abuse, illicit drug use, or any other condition (e.g., psychiatric disorder) that, in the opinion of the Investigator, may interfere with the patient's ability to comply with the study requirements or visit schedule.
• •Subjects with a known sensitivity to any of the study medication components.
• •Subjects known to have active HIV or known to be seropositive for HTLV-I.