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Can a milder transplant cure sickle cell and thalassemia in adults?

NCT ID NCT00061568

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 09, 2026 · Last updated Sep 10, 2026 · Updated 1 time

Summary

Researchers are testing a stem cell transplant that uses low-dose radiation and two immune-suppressing drugs instead of high-dose chemotherapy. The goal is to cure severe sickle cell disease and beta-thalassemia in adults up to age 65 who have a matched sibling donor. Participants receive donor stem cells after the gentler preparation, and researchers track whether the transplant cures the disease and what side effects occur.

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 alemtuzumab, sirolimus, and low-dose total body irradiation
What this could lead to
If it works, this approach could offer a cure for adults with severe sickle cell disease or beta-thalassemia who cannot tolerate standard bone marrow transplants.
What could go wrong
The transplant can cause graft-versus-host disease, where donor cells attack the patient's body, and the low-dose radiation and immune drugs carry their own risks. The trial is early stage, so success is not guaranteed.

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

130 people

The number who actually took part.

Started

Jul 2004

Expected to finish

Jan 2028

An estimate. End dates often move.

Lead sponsor

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

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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 from below: DISEASE SPECIFIC: Patients with sickle cell disease at high risk for disease related morbidity or mortality, defined by having irreversible end organ damage (A, B, C, D or E) or potentially reversible complication(s) not ameliorated by hydroxyurea (F): A. Stroke defined as a clinically significant neurologic event that is accompanied by and infarct on cerebral MRI OR an abnormal trans-cranial Doppler examination ( greater than or equal to 200m/s); 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 nephritic syndrome OR creatinine clearance less than 60mL/min/1.73m(2) for patients less than or equal to 16 years of age or less than 50mL/min for patients greater than or equal to 16 years of age OR requiring peritoneal or hemodialysis OR Age is less than or equal to 5 years of age with the upper limit of normal serum creatinine 0.8mg/dl Age is greater than 5 years or less than or equal to 10 years of age with the upper limit of normal serum creatinine 1.0mg/dl Age is greater than 10 years and less than or equal to 15 years of age the the upper limit of normal serum creatinine 1.2mg/dl Age greater than 15 years of age with the upper limit of normal serum creatinine 1.3mg/dl C. Tricuspid regurgitant jet velocity (TRV) of greater than or equal to 2.5m/s in patients greater than or equal to 18 years of age at least 3 weeks after a vaso-occlusive crisis, OR D. Recurrent tricorporal priapism defined as at least two episodes of an erection lasting greater than or equal to 4 hours involving the corpora cavernosa and corpus spongiosa, OR E. Sickle hepatopathy defined as EITHER ferritin greater than 100mcg/L OR direct bilirubin greater than 0.4 mg/dL at baseline in patients greater than or equal to 18 years of age; OR F. Any one of the below complications: 1. Vaso-occlusive crisis: * Eligible for hydroxyurea; at least 3 hospital admissions in the last year * Eligible for HSCT; More than 1 hospital admission per year while on therapeutic dose of hydroxyurea 2. Acute Chest Syndrome (ACS): * Eligible for hydroxyurea: 2 prior ACS while greater than 3 years of age and adequately treated for asthma * Eligible for HSCT: any ACS while on hydroxyurea\* 3. Osteonecrosis of 2 or more joints: * Eligible for hydroxyurea: And significantly affecting their quality of life by Karnofsky score 50-60 * Eligible for HSCT: And on hydroxyurea\* where total hemoglobin increase less than 1g/dL or fetal hemoglobin increases less than 2.5 time the baseline level 4. Red cell alloimmunization: * Eligible for hydroxyurea: Transfusion dependent * Eligible for HSCT: Total hemoglobin increase less than 1 g/dL while on hydroxyurea\* * hydroxyurea at therapeutic dose Patients with beta-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 desferoxamine 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 2 cm below the costochondral margin NON-DISEASE SPECIFIC: * Ages greater than or equal to 4 years * 6/6 HLA matched family donor available * Ability to comprehend and willing to sign an informed consent, assent obtained from minors * Negative serum beta-HCG * Pediatric patients less than 16 years of age must decline myeloablative bone marrow transplantation DONOR: Donor deemed suitable and eligible, and willing to donate per clinical evaluations, who are additionally willing to donate blood for research and undergo a neuropsychological test. Donors will be evaluated in accordance with existing Standard NIH Policies and Procedures for determination of eligibility and suitability for clinical donation under a separate NHLBI protocol. Note that participation in this study is offered to all donors, but is not required for a donor to make a stem cell donation, so it is possible that not all donors will enroll onto this study. EXCLUSION CRITERIA: RECIPIENT: (Any of the following would exclude the subject from participating) ECOG performance status of 3 or more or Lansky performance status of less than 40. Diffusion capacity of carbon monoxide (DLCO) less than 35% predicted. (corrected for hemoglobin and alveolar volume) Baseline oxygen saturation or less than 85 % or PaOa2 less than 70 Left ventricular ejection fraction: less than 35% estimated by ECHO. Transaminases greater than 5 times the upper limit of normal for age 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 Major anticipated illness or organ failure incompatible with survival from PBSC transplant. Pregnant or lactating Major ABO mismatch DONOR: None

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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

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.