RecruitingPhase 2

Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT

A Phase II Study of Reduced Intensity Conditioning in Pediatric Patients and Young Adults ≤55 Years of Age With Non-Malignant Disorders Undergoing Umbilical Cord Blood, Bone Marrow, or Peripheral Blood Stem Cell Transplantation

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
2 Months to 55 Years
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

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) bone marrow transplant (BMT) or peripheral blood stem cell transplant (PBSCT) in patients with non-malignant disorders that are amenable to treatment with hematopoietic stem cell transplant (HSCT). After transplant, subjects will be followed for late effects and for ongoing graft success.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Official eligibility criteria

Inclusion: 1. 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. 2. Adequate organ function as measured by: 1. Creatinine ≤ 2.0 mg/dL and creatinine clearance ≥ 50 mL/min/1.73 m2. 2. Hepatic transaminases (ALT/AST) ≤ 4 x upper limit of normal (ULN). 3. Adequate cardiac function by echocardiogram or radionuclide scan (shortening fraction \> 26% or ejection fraction \> 40% or \> 80% of normal value for age). 4. 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. 3. Written informed consent and/or assent according to FDA guidelines. 4. Negative pregnancy test if pubertal and/or menstruating. 5. HIV negative. 6. A non-malignant disorder amenable to treatment by stem cell transplantation, including but not limited to: 1. 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 2. Congenital bone marrow failure syndromes including but not limited to: * Dyskeratosis Congenita (DC) * Congenital Amegakaryocytic Thrombocytopenia (CAMT) * Osteopetrosis 3. 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. 4. 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 5. Inflammatory Conditions * Crohn's Disease/Inflammatory Bowel Disease Exclusion: 1. Allogeneic hematopoietic stem cell transplant within the previous 6 months. 2. Any active malignancy or MDS. 3. Severe acquired aplastic anemia. 4. Uncontrolled bacterial, viral or fungal infection (currently taking medication and with progression of clinical symptoms). 5. Pregnancy or nursing mother. 6. Poorly controlled pulmonary hypertension. 7. Any condition that precludes serial follow-up.

Study sites (1)

PA