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Hematopoietic Stem Cell BCL11A Enhancer Gene Editing for Sickle Cell Disease

13 de julio de 2026 actualizado por: Daniel Bauer

A Pilot Trial of Hematopoietic Stem Cell BCL11A Enhancer Gene Editing for Sickle Cell Disease

A promising approach for the treatment of genetic diseases is called gene therapy. Gene therapy is a relatively new field of medicine that uses genetic material (mostly DNA) from the patient to treat his or her own disease. In gene therapy, the investigators introduce new genetic material in order to fix or replace a diseased gene, with the goal of curing the disease. The procedure is similar to a bone marrow transplant, in that the patient's malfunctioning blood stem cells are reduced or eliminated using chemotherapy, but it is different because instead of using a different person's (donor) blood stem cells for the transplant, the patient's own blood stem cells are given back after the new genetic material has been introduced into those cells. This approach has the advantage of eliminating any risk of Graft-Versus-Host Disease (GVHD), reducing the risk of graft rejection, and may also allow less chemotherapy to be utilized for the conditioning portion of the transplant procedure. The method used to fix or replace a diseased gene is called gene editing. A person's own cells are edited using a specialized biological medicine that has been formulated for use in human beings.

Fetal hemoglobin (HbF) is a healthy, non-sickling kind of hemoglobin. Investigators have recently discovered a gene called BCL11A that is very important in the control of fetal hemoglobin expression. Increasing the expression of this gene in sickle cell patients could increase the amount of fetal hemoglobin while simultaneously reducing the amount of sickle hemoglobin in their blood, and therefore potentially cure the condition.

Descripción general del estudio

Descripción detallada

This is a non-randomized, single center, open-label, pilot safety and feasibility study involving a single infusion of autologous bone marrow derived CD34+ hematopoietic stem cells (HSPCs) electroporated with BCL11A enhancer targeting Cas9 ribonucleoprotein. Accrual will be a maximum of 5 evaluable subjects with sickle cell disease (SCD).

Ages ≥18-40 years: Stratum 1 (n=3) Ages ≥13-18 years: Stratum 2 (n=2)

After meeting eligibility criteria, patients will be enrolled. Patients will receive blood transfusions for a period of 3 months prior to hematopoietic stem cell collection, with a goal of achieving a Hemoglobin S (HbS) level of ≤ 30% by the time of mobilization. Patients will undergo peripheral stem cell mobilization and have their cells collected by apheresis. The collected cells of each subject will be split into 2 portions; one portion for gene editing, and one portion set aside as a back-up product in the event a rescue treatment is needed. Patients may undergo multiple rounds of collection if sufficient numbers of cells are not obtained with the first collection.

Patients will undergo a standard work-up for autologous bone marrow transplantation prior to proceeding with conditioning and infusion of their gene-edited cells. Patients will receive myeloablative conditioning with busulfan administered on days -5 to -2, prior to the infusion of edited cells. The edited cells will be infused intravenously.

Patients will be followed for 24 months after the infusion of their gene edited cells.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

5

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Massachusetts
      • Boston, Massachusetts, Estados Unidos, 02115
        • Boston Children's Hospital

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Diagnosis of either a) sickle cell disease with genotype HbSS, HbS/B0 thalassemia, HbSD, or HbSO
  2. Age 13-40 years.
  3. Clinically severe disease, defined as: The presence of one or more of the following clinical complications: i) Minimum of two episodes of acute chest syndrome (ACS) in the 2 years before study entry. ii) History of three or more episodes of severe pain events requiring a visit to a medical facility and treatment with parenteral opioids in the 2 years before study entry.
  4. Adequate hematologic parameters including:

    a. White blood cell (WBC) count within the range of 2.5 - 25.0 x 109 /L b. Platelet count within the range of 150 - 700 x 109 /L

  5. Adequate organ function and performance status:

    1. Karnofsky performance status ≥70%
    2. Serum creatinine </=1.5 times the upper limit of normal for age, and calculated creatinine clearance or GFR </= 60 mL/min/1.73 m2.
    3. Direct bilirubin ≤ 2.0 mg/dL
    4. DLCO (corrected for hemoglobin), FEV1, FVC >50% of predicted
    5. Left ventricular ejection fraction >40% or shortening fraction >25%
  6. Failure of hydroxyurea therapy due to lack of clinical improvement, inability to tolerate due to side effects (e.g., myelosuppression, gastrointestinal symptoms, or hepatic enzyme elevations) or not clinically indicated (such as in a patient on a chronic transfusion regimen). Clinical criteria (per above) must be met despite taking hydroxyurea for greater than or equal to 6 months, unless not indicated or not tolerated. Patients taking hydroxyurea who still meet all inclusion criteria are eligible for the trial. Hydroxyurea should be discontinued when transfusions prior to gene therapy begin.
  7. Confirmed sickle cell disease diagnosis by molecular genetic testing.
  8. No HLA genotypically-identical related appropriate bone marrow donor available.
  9. Parental/guardian/patient signed informed consent.
  10. Willingness to return for follow-up for 15 years.

Exclusion Criteria:

  1. Subjects who have concomitant condition or illness including, but not limited to:

    1. Uncontrolled infection, such as current febrile illness, infection requiring parenteral antibiotics, or systemic fungal infection.
    2. Active malignancy.
    3. Active complication of underlying hemoglobinopathy that would place the patient at unacceptable risk for participation, in the judgment of the Investigators.
    4. Major surgery in the past 30 days.
    5. Medical/psychiatric illness/social situations that would limit compliance with study requirements as determined by the treating physician.

      • Contraindication to administration of conditioning medication (busulfan).

3. Subjects who have undergone allogeneic or autologous hematopoietic stem cell transplant previously.

4. Either or both of the following findings on screening bone marrow aspirate/biopsy: a) diagnosis of myelodysplastic syndrome (MDS) based on morphology and/or cytogenetics (based on WHO definitions) or b) pathogenic mutation in any gene on the Rapid Heme Panel (RHP), a next-generation targeted sequencing clinical assay for hematologic malignancy associated mutations.

5. For SCD patients:

  1. Severe cerebral vasculopathy (defined by occlusion or stenosis in the circle of Willis; or presence of Moyamoya disease)
  2. Receiving a chronic transfusion regimen for primary or secondary stroke prophylaxis. (Note: patients with a history of abnormal transcranial Doppler (TCD) who have transitioned from transfusions to hydroxyurea for stroke prophylaxis are also not eligible for the study. Most recent TCD must be within one year of screening for patients up to 16 years old.)
  3. History of overt stroke or any neurologic event lasting > 24 hours. (Note: patients with imaging evidence of silent stroke but not on a chronic transfusion regimen are not excluded.) 6. Severe iron overload that is deemed to be grounds for exclusion based on the opinion of the Principal Investigator.

    7. Known positive HIV serology or HIV nucleic acid testing, or positive serology for HCV, HBV, or HTLV.

    8. Known acute hepatitis or evidence of moderate or severe portal fibrosis or cirrhosis on prior biopsy.

    9. Receipt of an investigational study drug or procedure within 90 days of study enrollment.

    10. Pregnancy, or breastfeeding in a postpartum female, or absence of adequate contraception for fertile subjects. Females of child-bearing potential must agree to use a medically acceptable method of birth control such as oral contraceptive, intrauterine device, barrier and spermicide, or contraceptive implant/injection from Screening through at least 6 months after drug product infusion. Male subjects must agree to use effective contraception (including condoms) from Screening through at least 6 months after drug product infusion.

    11. An assessment by the Investigators that the subject will not comply with the study procedures outlined in the study protocol, or that, as determined by the investigators and/or transplant physician, the subject has any other condition rendering the subject ineligible for HSCT or other study procedures.

    12. Patients carrying at least one cytosine (C) alternate allele at the SNP site rs114518452, chr2:210530659-210530659 (GRCh38/hg38), where guanine (G) is the reference allele.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Sickle Cell Disease
HSPC CD34+ autólogas derivadas de médula ósea electroporadas con potenciador BCL11A dirigido a la ribonucleoproteína Cas9
Dispositivo utilizado para realizar las pruebas diagnósticas del criterio de exclusión número 12

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Injerto primario
Periodo de tiempo: 42 dias
Reconstitución hematopoyética exitosa después del acondicionamiento (definida por un recuento absoluto de neutrófilos (RAN) mayor o igual a 0,5 x 10 ^ 9 /L durante tres días consecutivos sin soporte de factor de crecimiento), lograda el día 42 después del día 0 de la infusión de células madre (es decir, "injerto primario").
42 dias

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Hemoglobina
Periodo de tiempo: 24 meses
Hemoglobina total (en g/dL), fracciones de hemoglobina (A, F y S en g/dL), porcentaje de HbF y porcentaje de células F
24 meses
Injerto de plaquetas
Periodo de tiempo: 42 dias
Injerto de plaquetas (definido como recuento de plaquetas ≥20 000/l sin transfusión durante 7 días por día +42 después de la infusión de células madre)
42 dias
Calidad de vida
Periodo de tiempo: 24 meses
Calidad de vida, evaluada por la administración de la herramienta de encuesta PEDSQL al paciente (o padres de niños pequeños) para sujetos menores de 18 años, y por la administración de la herramienta de encuesta SF-36 para sujetos adultos
24 meses
Severe vaso-occlusive crises
Periodo de tiempo: 24 months
Change from baseline in incidence of severe vaso-occlusive crises (requiring emergency department visit or hospital admission)
24 months
Acute chest syndrome
Periodo de tiempo: 24 months
Change from baseline in incidence of acute chest syndrome
24 months
Stroke
Periodo de tiempo: 24 months
Change from baseline in incidence of stroke
24 months
Splenic sequestration
Periodo de tiempo: 24 months
Change from baseline in incidence of splenic sequestration
24 months
Transfusion requirement
Periodo de tiempo: 24 months
Change from baseline in transfusion requirement (in mL/kg) after day +100 post infusion
24 months
Reticulocyte count
Periodo de tiempo: 24 months
Change from baseline reticulocyte count
24 months
Bilirubin
Periodo de tiempo: 24 months
Change from baseline bilirubin
24 months
Lactate dehydrogenase (LDH)
Periodo de tiempo: 24 months
Change from baseline lactate dehydrogenase (LDH)
24 months

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Resultado de seguridad: muerte
Periodo de tiempo: 24 meses
Ocurrencia de muerte
24 meses
Resultado de seguridad: eventos adversos graves
Periodo de tiempo: 24 meses
Número de eventos adversos graves
24 meses
14. Safety Outcome: Malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
Periodo de tiempo: 24 months
Occurrence of malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
24 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de agosto de 2026

Finalización primaria (Estimado)

1 de diciembre de 2028

Finalización del estudio (Estimado)

1 de diciembre de 2030

Fechas de registro del estudio

Enviado por primera vez

13 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

13 de julio de 2026

Publicado por primera vez (Actual)

16 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

16 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

13 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

Sí

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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