Can a softer transplant cure sickle cell disease?
NCT ID NCT04362293
First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time
Summary
This trial tests a stem cell transplant method that uses lower doses of chemotherapy and radiation, aiming to reduce side effects while still replacing the faulty blood cells that cause sickle cell disease. Children and young adults up to age 25 with severe sickle cell disease can join if they have a suitable donor, either a matched sibling or a half-matched family member. The study measures how well donor cells take hold and whether the disease stays away for up to three years after the transplant.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A stem cell transplant using donor blood stem cells, with a conditioning regimen of hydroxyurea, azathioprine, alemtuzumab, thiotepa, low-dose total body irradiation, and sirolimus.
- What this could lead to
- If successful, this could offer a cure for severe sickle cell disease with fewer side effects than standard transplants, potentially replacing the need for lifelong disease management.
- What could go wrong
- The trial is early (Phase 2) and small, so results may not hold in larger groups. Risks include graft rejection, graft-versus-host disease, and side effects from the conditioning drugs.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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46 people
The number who actually took part.
- Started
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Apr 2020
- Expected to finish
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Aug 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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2 to 25 years
- Sex
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Anyone
- Healthy volunteers
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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 for Transplant Recipient * Age less than or equal to 25 years. * Patients with a suitable HLA-matched sibling donor (MSD) can be enrolled on MSD arm of the trial. Patients with single haplotype matched (≥ 3 of 6) family member donor can be enrolled on HAPLO arm of the trial, if they do not have a suitable HLA-matched sibling donor (MSD) available for progenitor cell donation. * Patients with SCD (any genotype) who meet any ONE of the following criteria: 1. History of an abnormal transcranial Doppler measurement defined as TCD velocity ≥ 200 cm/sec by the non-imaging technique (or ≥ 185 cm/sec by the imaging technique) measured at a minimum of two separate occasions. 2. History of cerebral infarction on brain MRI (overt stroke, or silent stroke if ≥3 mm in one dimension, visible in two planes on fluid-attenuated inversion recovery T2- weighted images). 3. History of two or more episodes of acute chest syndrome (ACS) in the 2-years period preceding enrollment. 4. History of two or more SCD pain events requiring treatment with an opiate or IV pain medication (inpatient or outpatient) in the last 12 months. 5. History of any hospitalization for SCD pain or ACS while receiving hydroxyurea treatment in the last 12 months. 6. History of two or more episodes of priapism (erection lasting ≥4 hours or requiring emergent medical care). 7. Administration of regular RBC transfusions (≥8 transfusions in the previous 12 months). 8. At least two episodes of splenic sequestration requiring red blood cell transfusion or splenectomy after at least one episode of splenic sequestration. Exclusion Criteria for Transplant Recipient * Karnofsky or Lansky performance score \<60. * Pregnant or breastfeeding patients. * Uncontrolled bacterial, viral or fungal infections (undergoing appropriate treatment and with progression of clinical symptoms) within 1 month prior to conditioning. Patients with febrile illness or suspected minor infection should await clinical resolution prior to starting conditioning. Patients with confirmed seropositivity or positive NAAT for HIV are excluded. * Serum conjugated (direct) bilirubin \>3x upper limit of normal for age as per local laboratory. Participants with hyperbilirubinemia or elevated AST as the result of hyperhemolysis, or a severe drop in hemoglobin post blood transfusion, are not excluded as long as it downtrends and return to acceptable limits subsequently. * Left ventricular shortening fraction \<25% or ejection fraction \<40% by echocardiogram. * Estimated creatinine clearance less than 50 mL/min/1.73m2. * Diffusion capacity of carbon monoxide (DLCO) \<35% (adjusted for hemoglobin). Baseline oxygen saturation \<85% or PaO2 \<70. * Presence of anti-donor specific HLA antibodies unresponsive to desensitization as defined below. HLA antibody presence and specificity will be determined by solid phase immunoassays. An anti-donor specific HLA antibody test will be considered positive when the mean fluorescence intensity (MFI) is: * \>1,000 for donor specific antibodies to HLA-A, -B, and DRB1. or * \>2,000 for donor specific antibodies to HLA-C, DQB1 and DPB1. A participant with presence of anti-donor specific HLA antibodies may be provisionally enrolled on the study if desensitization (see Appendix H) is begun concurrently with pre-conditioning. Response to desensitization will be defined as: * decreasing anti-donor specific HLA antibody titer with an MFI of less than 5,000 and * negative C1q-binding anti-HLA antibody assay. Inclusion Criteria for Donor * An HLA-matched sibling donor for MSD arm and at least single haplotype matched (≥ 3 of 6) family member for HAPLO arm. * HIV negative. * Not pregnant as confirmed by negative serum or urine pregnancy test within 14 days prior to enrollment (if female). * Not breast feeding. * Donor should not have clinically significant hemoglobinopathy. Donors with sickle cell trait are acceptable.
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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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St. Jude Children's Research Hospital
Memphis, Tennessee, 38105, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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