Status:
RECRUITING
Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT
Lead Sponsor:
Paul Szabolcs
Conditions:
Primary Immunodeficiency (PID)
Congenital Bone Marrow Failure Syndromes
Eligibility:
All Genders
2-55 years
Phase:
PHASE2
Brief Summary
The objective of this study is to evaluate the efficacy of using a reduced-intensity condition (RIC) regimen with umbilical cord blood transplant (UCBT), double cord UCBT, matched unrelated donor (MUD...
Detailed Description
For some non-malignant diseases (NMD; i.e., thalassemia, sickle cell disease, most immune deficiencies) a hematopoietic stem cell transplant may be curative by healthy donor stem cell engraftment alon...
Eligibility Criteria
Inclusion:
-
A 4/6, 5/6 or 6/6 HLA matched related or unrelated UCB unit available that will deliver a pre-cryopreservation total nucleated cell dose of ≥ 3 x 10e7 cells/kg, or double unit grafts, each cord blood unit delivering at least 2 x 10e7 cells/kg OR an 8 of 8 or 7 of 8 HLA allele level matched unrelated donor bone marrow or peripheral blood progenitor graft.
-
Adequate organ function as measured by:
- Creatinine ≤ 2.0 mg/dL and creatinine clearance ≥ 50 mL/min/1.73 m2.
- Hepatic transaminases (ALT/AST) ≤ 4 x upper limit of normal (ULN).
- Adequate cardiac function by echocardiogram or radionuclide scan (shortening fraction > 26% or ejection fraction > 40% or > 80% of normal value for age).
- Pulmonary evaluation testing demonstrating CVC or FEV1/FVC of ≥ 50% of predicted for age and/or resting pulse oximeter ≥ 92% on room air or clearance by the pediatric or adult pulmonologist. For adult patients DLCO (corrected for hemoglobin) should be ≥ 50% of predicted if the DLCO can be obtained.
-
Written informed consent and/or assent according to FDA guidelines.
-
Negative pregnancy test if pubertal and/or menstruating.
-
HIV negative.
-
A non-malignant disorder amenable to treatment by stem cell transplantation, including but not limited to:
-
Primary Immunodeficiency syndromes including but not limited to:
- Severe Combined Immune Deficiency (SCID) with NK cell activity
- Omenn Syndrome
- Bare Lymphocyte Syndrome (BLS)
- Combined Immune Deficiency (CID) syndromes
- Combined Variable Immune Deficiency (CVID) syndrome
- Wiskott-Aldrich Syndrome
- Leukocyte adhesion deficiency
- Chronic granulomatous disease (CGD)
- X-linked Hyper IgM (XHIM) syndrome
- IPEX syndrome
- Chediak - Higashi Syndrome
- Autoimmune Lymphoproliferative Syndrome (ALPS)
- Hemophagocytic Lymphohistiocytosis (HLH) syndromes
- Lymphocyte Signaling defects
- Other primary immune defects where hematopoietic stem cell transplantation may be beneficial
-
Congenital bone marrow failure syndromes including but not limited to:
- Dyskeratosis Congenita (DC)
- Congenital Amegakaryocytic Thrombocytopenia (CAMT)
- Osteopetrosis
-
Inherited Metabolic Disorders (IMD) including but not limited to:
-
Mucopolysaccharidoses
- Hurler syndrome (MPS I)
- Hunter syndrome (MPS II)
-
Leukodystrophies
- Krabbe Disease, also known as globoid cell leukodystrophy
- Metachromatic leukodystrophy (MLD)
- X-linked adrenoleukodystrophy (ALD)
- Hereditary diffuse leukoencephalopathy with spheroids (HDLS)
-
Other inherited metabolic disorders
- alpha mannosidosis
- Gaucher Disease
-
Other inheritable metabolic diseases where hematopoietic stem cell transplantation may be beneficial.
-
-
Hereditary anemias
-
Thalassemia major
-
Sickle cell disease (SCD) - patients with sickle disease must have one or more of the following:
- Overt or silent stroke
- Pain crises ≥ 2 episodes per year for past year
- One or more episodes of acute chest syndrome
- Osteonecrosis involving ≥ 1 joints
- Priapism
-
Diamond Blackfan Anemia (DBA)
-
Other congenital transfusion dependent anemias
-
-
Inflammatory Conditions
- Crohn's Disease/Inflammatory Bowel Disease
-
Exclusion:
- Allogeneic hematopoietic stem cell transplant within the previous 6 months.
- Any active malignancy or MDS.
- Severe acquired aplastic anemia.
- Uncontrolled bacterial, viral or fungal infection (currently taking medication and with progression of clinical symptoms).
- Pregnancy or nursing mother.
- Poorly controlled pulmonary hypertension.
- Any condition that precludes serial follow-up.
Key Trial Info
Start Date :
February 4 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2027
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT01962415
Start Date
February 4 2014
End Date
November 1 2027
Last Update
December 15 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
UPMC Children's Hospital of Pittsburgh
Pittsburgh, Pennsylvania, United States, 15224