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NCT05736419RecruitingPhase 2

A Study of Immune Suppression Treatment for People With Sickle Cell Disease or β-Thalassemia Who Are Going to Receive an Allogeneic Hematopoietic Cell Transplantation (HCT)

Pre-Transplant Immune Suppression With Hematopoietic Cell Transplantation From Haploidentical Donors for Adults and Children With Sickle Cell Disease or ß-Thalassemia (Haplo PTCy)

Source: ClinicalTrials.gov · Last updated 3 Jun 2026

Brief summary (registry, in English)

Hematopoietic Cell Transplantation/HCT involves receiving healthy blood-forming cells (stem cells) from a donor to replace the diseased or damaged cells in participants' bone marrow. The researchers think giving participants treatment with fludarabine and dexamethasone, drugs that lower the activity of the body's immune system (immune suppression), before standard conditioning therapy and HCT may help prevent serious side effects, including graft failure and GvHD. In this study, depending on how participants' body responds to the fludarabine and dexamethasone, the study doctor may decide participants should receive another drug, called cyclophosphamide, instead of fludarabine. In addition, depending on the results of participants' routine blood tests, participants may receive the drugs bortezomib and rituximab, which also help with immune suppression.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
24 (estimated)
First submitted
9 Feb 2023
Start date
9 Feb 2023
Primary completion date
9 Feb 2027
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT05736419

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 24
  • From 9 Feb 2023 to the primary completion date, 9 Feb 2027
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior myeloablative allogeneic HCT.
  • Positive pregnancy test in a woman with child-bearing potential, defined as not post-menopausal for 12 months or no previous surgical sterilization.
  • Inability to comply with medical therapy or follow-up.

Other illness

  • Overt stroke or CNS instrumentation (e.g. for Moyamoya disease) within 6 months of enrollment.
  • Active hepatitis B or C.
  • Other uncontrolled infections.
  • Other malignancy/cancer diagnosis unless in remission after definitive therapy for a minimum of 2 years. Exceptions: Ductal carcinoma in situ, basal cell carcinoma, cervical intraepithelial neoplasia.
  • Known history of allergic reactions to any constituents of the stem cell product, including a known history of allergic reactions to DMSO.

Other

  • Liver cirrhosis. Mild fibrosis will be permitted, i.e. fine reticulin or grade 1 of 4, with bridging fibrosis.
  • Hepatic iron content ≥ 3 mg Fe/g liver dry weight, if applicable

Who the study is looking for

  • Age ≥ 2 and ≤ 50 years
  • Suitable haploidentical donor.
  • Performance score ≥ 70% by Karnofsky Performance Scale or 0 to 1 by ECOG (age \> 16 years), or Lansky Play-Performance Scale ≥ 70% (age ≤ 16 years).
  • Adequate major organ system function as demonstrated by:
    • For patients ≥ 18 years of age:
    • eGFR ≥ 50 mL/min by Cockcroft-Gault formula Formula: ((140 - Age) x Weight (kg)) / (72 x Serum Creatinine (mg/dL) Female Adjustment: Multiply result by 0.85
    • For patients \< 18 years of age:
    • Serum creatinine clearance: glomerular filtration rate \[GFR\]) must be \>50 mL/min/1.73 m2 as calculated by the Schwartz formula
  • Conjugated (direct) bilirubin less than 3x upper limit of normal.
  • ALT or AST ≤ 3 times institutional upper limit of normal.
  • Left ventricular ejection fraction ≥ 50%.
  • Diffusing capacity for carbon monoxide (DLCO) ≥ 50% predicted, corrected for hemoglobin. For children \< 7 years of age who are unable to perform PFT, oxygen saturation \> 92% on room air by pulse oximetry.
  • For SCD patients: HbSS, HbSC, HbS/β° with one or more of the following complications:
    • Acute chest syndrome: 2 or more episodes in the 2 years preceding enrollment
    • Vaso-occlusive episodes: 3 or more episodes in the 2 years preceding enrollment
    • Recurrent priapism: 2 or more episodes in the 2 years preceding enrollment
    • History of osteomyelitis or osteonecrosis
    • Cerebrovascular disease:
  • Imaging evidence of prior overt or silent stroke
  • History of a neurologic event resulting in focal neurologic deficits lasting \> 24 hours
  • Abnormal transcranial Doppler: Timed average maximum mean velocity ≥ 200 cm/sec in terminal portion of the carotid or proximal portion of the middle cerebral artery or \> 185 cm/sec plus evidence of intracranial vasculopathy if imaging TCD is used
    • Pulmonary hypertension: Confirmed by right heart catheterization with mean pulmonary arterial pressure ≥ 25 mmHg or mean pulmonary vascular resistance \> 2 Wood units
    • Red blood cell alloimmunization (\> 3 alloantibodies)
  • For thalassemia patients: Any genotype, with all of the following:
    • Onset of red blood cell transfusion dependence during the first 3 years of life
    • RBC transfusion history \> 225 mL/kg/year or \> 15 lifetime RBC transfusions
    • Pre-transfusion hemoglobin ≤ 7 g/dL
    • Hepatosplenomegaly
  • Patient or the patient's legal representative, parent(s) or guardian should be able to provide written informed consent. Assent of a minor if participant's age is at least seven and less than eighteen years.
  • For sexually active men and women of childbearing potential, must agree to use a form of contraception considered effective and medically acceptable by the Investigator.

Age in the registry: 2 years to 50 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan Kettering at Basking Ridge (Consent Only)
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesRecruiting
Memorial Sloan Kettering Suffolk - Commack (Consent Only)
Coordinator of this site? Confirm its status
CommackUnited StatesRecruiting
Memorial Sloan Kettering Westchester (Consent only)
Coordinator of this site? Confirm its status
HarrisonUnited StatesRecruiting
Memorial Sloan Kettering Monmouth (Consent Only)
Coordinator of this site? Confirm its status
MiddletownUnited StatesRecruiting
Memorial Sloan Kettering Bergen (Consent Only)
Coordinator of this site? Confirm its status
MontvaleUnited StatesRecruiting
Memorial Sloan Kettering Nassau (All Protocol Activities)
Coordinator of this site? Confirm its status
Rockville CentreUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.