Safety and Efficacy of POL6326 for Mobilization/Transplant of Sibling Donor in Patients With Hematologic Malignancies

Inclusion Criteria

• •Donor must be 18 to 70 years of age inclusive.
• •Donor must be a 6/6 HLA-matched sibling willing to donate PBSC for transplant.
• •Donor must have adequate cardiac function with no history of congestive heart failure and no history of atrial fibrillation or ventricular tachyarrhythmia.
• •Donor must have adequate renal function as defined by a minimum creatinine clearance (CrCl) value of \>30 ml/min.
• •Donor must have adequate hepatic function as defined by a total bilirubin \<3x upper limit of normal.
• •Donor must have adequate neurologic function as defined by NO evidence of a severe central or peripheral neurologic abnormality and no history of cerebrovascular accident or seizure disorder requiring anticonvulsant medication.
• •Donor must be HIV-1\&2 antibody and HTLV-1\&2 antibody sero-negative by FDA licensed test.
• •Donor must have an ECOG performance status of 0 or 1.
• •Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.
• •Donor must demonstrate ability to be compliant with study regimen.
• •Donor must be able to understand and willing to sign an IRB approved written informed consent document.
• •Recipient must have available the successful collection of a POL62326 mobilized product.
• •Recipient must be 18 to 75 years of age inclusive.
• •Recipient must have a 6/6 HLA-matched sibling willing to donate PBSC for transplant.
• •Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.
• •Recipient must have one of the following diagnoses:
• •Acute myelogenous leukemia (AML) in 1st or subsequent remission
• •Acute lymphoblastic leukemia (ALL) in 1st or subsequent remission
• •Chronic myelogenous leukemia (CML)
• •Non-Hodgkin's lymphoma (NHL) or Hodgkin's disease (HD) in 2nd or greater complete remission, partial remission
• •Chronic lymphocytic leukemia (CLL)
• •Multiple myeloma (MM)
• •Myelodysplastic syndrome (MDS)
• •Myeloproliferative disorder (MPD)
• •Recipient must have adequate cardiac function with a left ventricular ejection fraction \> 40%.
• •Recipient must have adequate pulmonary function defined as NO severe or symptomatic restrictive or obstructive lung disease, and formal pulmonary function testing showing an FEV1 \>50% (predicted) and a DLCO \>40% (predicted), corrected for hemoglobin.
• •Recipient must have adequate hepatic function as defined by a total bilirubin \<3x upper limit of normal or absence of hepatic fibrosis/cirrhosis.
• •Recipient must have adequate neurologic function as defined by NO evidence of a severe central or peripheral neurologic abnormality. Patients with a history of previous CNS tumor involvement are eligible provided they are without symptoms or signs and the CNS is now free of disease on lumbar puncture and CT scan of the brain.
• •Recipient must be HIV-1\&2 antibody and HTLV-1\&2 antibody sero-negative by FDA licensed test.
• •Recipient must have an ECOG performance status of 0 or 1.
• •Recipient must demonstrate ability to be compliant with medical regimen.
• •Recipient must have life expectancy of greater than 2 months.
• •Recipient must be able to understand and willing to sign an IRB approved written informed consent document.