New stem cell transplant could help sickle cell patients without a perfect donor match
NCT ID NCT00977691
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a stem cell transplant using cells from a half-matched family donor, combined with low-dose radiation and drugs to prevent rejection, for adults with severe sickle cell disease or beta-thalassemia. The goal is to see if this gentler approach can replace the diseased cells without the high toxicity of standard chemotherapy. Twenty-three participants will be followed for five years to check if the donor cells survive and reduce disease symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- stem cell transplant (from a half-matched donor) with alemtuzumab, sirolimus, cyclophosphamide, and low-dose radiation
- What this could lead to
- If successful, this approach could offer a treatment option for sickle cell disease and beta-thalassemia patients who lack a fully matched donor, potentially reducing disease complications.
- What could go wrong
- This is an early-phase trial with only 23 participants, so results may not apply broadly. The transplant carries risks like graft rejection, infection, and side effects from immunosuppressant drugs.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
-
23 people
The number who actually took part.
- Started
-
Dec 2009
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
2 to 80 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* INCLUSION CRITERIA: Recipients (must fulfill one disease category in 5.1.1 and all of 5.1.2) 5.1.1 Disease specific 5.1.1.1 Patients with sickle cell disease (HB SS, SC, or SBeta(0)-thal) at high risk for disease-related morbidity or mortality, defined by having severe end-organ damage (A, B, C, or D) or potentially modifiable complication(s) not ameliorated by hydroxyurea (E): A. Stroke defined as a clinically significant neurologic event that is accompanied by an infarct on cerebral MRI or cerebral arteriopathy requiring chronic transfusion therapy; OR B. Sickle cell-related renal insufficiency defined by a creatinine level greater than or equal to 1.5 times the upper limit of normal and kidney biopsy consistent with sickle cell nephropathy OR nephrotic syndrome OR creatinine clearance less than 50mL/min OR requiring peritoneal or hemodialysis; OR C. Pulmonary hypertension defined as tricuspid regurgitant jet velocity (TRV) of greater than or equal to 2.5 m/s at baseline (without vaso-occlusive crisis); OR D. Sickle hepatopathy defined as EITHER ferritin greater than 1000mcg/L OR direct bilirubin greater than 0.4 mg/dL AND platelet count less than 250,000/microL at baseline (without vaso-occlusive crisis) E. Any one of the below complications: -Complication: Vaso-occlusive crises; Eligible for hydroxyurea\*: At least 3 hospital admissions in the last year. Eligible for HSCT: More than 1 hospital admission per year while on maximal tolerated dose of hydroxyurea\* -Complication: Acute chest syndrome Eligible for hydroxyurea\*: 2 prior ACS Eligible for HSCT: any ACS while on hydroxyurea\* \*hydroxyurea at maximum tolerated dose for at least 6 months 5.1.1.2 Patients with thalassemia who have grade 2 or 3 iron overload, determined by the presence of 2 or more of the following: * portal fibrosis by liver biopsy * inadequate chelation history (defined as failure to maintain adequate compliance with chelation with deferoxamine initiated within 18 months of the first transfusion and administered subcutaneously for 8-10 hours at least 5 days each week) * hepatomegaly of greater than 2cm below the costochondral margin 5.1.2 Non-disease specific: 5.1.2.1 Age greater than or equal to 18 years 5.1.2.2 Haploidentical relative donor available 5.1.2.3 Ability to comprehend and willing to sign an informed consent 5.1.2.4 Negative Beta-HCG EXCLUSION CRITERIA: Recipient (any of the following would exclude the subject from participating) 5.2.1 6/6 HLA-matched with or without an ABO minor mismatched sibling donor 5.2.2 ECOG performance status of 3 or more 5.2.3 Evidence of uncontrolled bacterial, viral, or fungal infections (currently taking medication and progression of clinical symptoms) within one month prior to starting the conditioning regimen. Patients with fever or suspected minor infection should await resolution of symptoms before starting the conditioning regimen. 5.2.4 Major anticipated illness or organ failure incompatible with survival from PBSC transplant 5.2.5 Pregnant or lactating 5.2.6 Major ABO mismatch INCLUSION CRITERIA: Donor 5.3.1 Haploidentical relative donor 5.3.2 Weight greater than or equal to 20 kg (insofar that the weight difference between recipient and donor does not exceed a reasonable likelihood of being able to obtain an adequate cell dose from the donor within two aphereses) 5.3.3 Fit to receive filgrastim (G-CSF) and to give peripheral blood stem cells (blood counts and blood pressure within DTM standards) 5.3.4 No history of congestive heart failure or unstable angina, and no history of stroke) 5.3.4 Ability to comprehend and willing to sign an informed consent; assent obtained from minors EXCLUSION CRITERIA: Donor: (any of the following would exclude the donor from participating) 5.4.1 Pregnant or lactating 5.4.2 HIV positive 5.4.3 Hemoglobin S greater than or equal to 50 percent, or beta thalassemia intermedia
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, 20892, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a single stem cell infusion rewrite the code of beta thalassemia?
- A gentler transplant may cure sickle cell and thalassemia — can the body accept donor cells?
- Mismatched donor stem cell transplant could widen treatment access for sickle cell disease
- How does a blood disorder drug perform in everyday practice?
- Newborn screening study aims to catch rare diseases at birth
- New sickle cell drug candidate enters first human tests