Trial of a Single ProHema-CB Unit as Part of a Double CB Transplant in Patients With Hematologic Malignancies
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Purpose
This study is an open-label randomized, prospectively and historically controlled trial of the safety and efficacy of a single ProHema-CB unit used as part of a double CB transplant following myeloablative conditioning for subjects age 15-55 years with hematologic malignancies. A maximum of 45 eligible subjects will be enrolled and treated in the trial at approximately 6-10 centers within the U.S.
| Condition | Intervention | Phase |
|---|---|---|
|
Hematologic Malignancies |
Biological: ProHema-CB Biological: Untreated CB |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase 2, Controlled Trial, Of A Single Prohema-CB Unit (Ex Vivo CXCR4-Upregulated CD34+ Hematopoietic Progenitor Cells, Cord Blood) As Part Of A Double Umbilical Cord Blood Transplant Following Myeloablative Conditioning For Patients Age 15-55 Years With Hematologic Malignancies |
- Neutrophil engraftment/chimerism [ Time Frame: Day 26 ] [ Designated as safety issue: No ]To determine the rate of neutrophil engraftment by Day 26 after a single ProHema-CB unit is used as part of a double CB transplant following myeloablative conditioning for subjects age 15-55 years with hematologic malignancies.
- Neutrophil engraftment [ Time Frame: Day 42 ] [ Designated as safety issue: No ]To define measures of engraftment, including time to neutrophil engraftment, cumulative incidence of neutrophil engraftment by Day 42, time to platelet engraftment (> 20K and > 50K), cumulative incidence of platelet engraftment by Day 180, and rates of primary and secondary graft failure
| Estimated Enrollment: | 10 |
| Study Start Date: | July 2012 |
| Study Completion Date: | May 2013 |
| Primary Completion Date: | May 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: ProHema-CB |
Biological: ProHema-CB
Ex-vivo CXCR4 upregulated hematopoietic progenitor cells, cord blood
|
| Active Comparator: Control Arm |
Biological: Untreated CB
Cord Blood
|
Detailed Description:
All subjects will receive a myeloablative conditioning regimen, after which they will receive 2 HLA-matched UCB units. A total of 30 subjects will receive one ProHema-CB as part of a double CB transplant and an additional 15 subjects will be enrolled as concurrent controls. The determination of which CB unit will be the ProHema-CB unit will be made based primarily upon the degree of HLA match.
Eligibility| Ages Eligible for Study: | 15 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Subjects with hematologic malignancies for whom allogeneic stem cell transplantation is deemed clinically appropriate. Eligible diseases and stages include:
- Acute lymphoblastic leukemia (including T lymphoblastic leukemia) in complete remission.
- Remission is defined as < 5% blasts with no morphological characteristics of acute leukemia in a bone marrow with > 20% cellularity.
- Acute myelogenous leukemia in high risk first CR or second or subsequent CR.
- High risk first CR is defined by but is not limited to at least one of the following factors: greater than 1 cycle of induction chemotherapy to achieve CR, prior myelodysplastic syndrome (MDS), presence of Flt3 abnormalities, FAB M6 or M7 subtypes of leukemia, or adverse cytogenetics.
- Remission is defined as < 5% blasts with no morphological characteristics of acute leukemia (e.g. Auer Rods) in a bone marrow with > 20% cellularity.
- Biphenotypic/Undifferentiated leukemia in first or subsequent CR (same definition of CR as for ALL/AML).
- Non-Hodgkin's lymphoma (T-cell, large cell or mantle cell) or Hodgkin's lymphoma in second or subsequent complete remission (CR) or in partial remission (PR) with documented chemosensitivity. In addition, marginal zone lymphoma or follicular lymphoma that has progressed after ≥ 2 therapies (excluding single-agent rituximab). No history of prior myeloablative procedure.
- Lack of suitable 5-6/6 HLA-matched related or (if institutional guidelines dictate) suitable 8/8 HLA-A, B, C, DRß1 matched unrelated donor; or unrelated donor not available within appropriate timeframe.
- Age 15-55 years.
- Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
- Signed IRB approved Informed Consent Form (ICF).
Exclusion Criteria:
- History of prior allogeneic transplantation
- Cardiac disease: symptomatic congestive heart failure or evidence of left ventricular dysfunction (Ejection fraction < 40%) as measured by gated radionuclide ventriculogram or echocardiogram; active angina pectoris, or uncontrolled hypertension; history of myocardial infarction with depressed ejection fraction.
- Pulmonary disease: symptomatic chronic obstructive lung disease, symptomatic restrictive lung disease, or corrected DLCO of < 50% of predicted, corrected for hemoglobin.
- Renal disease: serum creatinine > 2.0 mg/dl and calculated creatinine clearance < 40 mL/min.
- Hepatic disease: serum bilirubin > 2.0 mg/dl (except in the case of Gilbert's syndrome or ongoing hemolytic anemia), SGOT or SGPT > 5 x upper limit of normal.
- Neurologic disease: symptomatic leukoencephalopathy, active CNS malignancy or other neuropsychiatric abnormalities believed to preclude transplantation.
- HIV antibody.
- Uncontrolled infection.
- Pregnancy or breast feeding mother.
- Inability to comply with the requirements for care after allogeneic stem cell transplantation.
Contacts and Locations| United States, California | |
| City of Hope | |
| Duarte, California, United States | |
| United States, Massachusetts | |
| Dana-Farber Cancer Institute- Hematopoietic Stem Cell Transplant Program | |
| Boston, Massachusetts, United States, 02215 | |
| Massachusetts General Hospital | |
| Boston, Massachusetts, United States, 02114 | |
| United States, Missouri | |
| Washington University School of Medicine | |
| St Louis, Missouri, United States | |
| United States, New York | |
| Mount Sinai Hospital | |
| New York, New York, United States, 10029 | |
| United States, Ohio | |
| Ohio State University Comprehensive Cancer Center | |
| Columbus, Ohio, United States, 43210 | |
| United States, Oregon | |
| Oregon Health Sciences | |
| Portland, Oregon, United States | |
| Study Director: | Pratik Multani, MD | Fate Therapeutics |
More Information
No publications provided
| Responsible Party: | Fate Therapeutics |
| ClinicalTrials.gov Identifier: | NCT01627314 History of Changes |
| Other Study ID Numbers: | FT1050-03 |
| Study First Received: | June 21, 2012 |
| Last Updated: | May 10, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Neoplasms Hematologic Neoplasms Neoplasms by Site Hematologic Diseases |
ClinicalTrials.gov processed this record on May 19, 2013