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Hematopoietic Stem Cell BCL11A Enhancer Gene Editing for Sickle Cell Disease

2026년 7월 13일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

5

단계

  • 1단계

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연구 연락처

연구 장소

    • Massachusetts
      • Boston, Massachusetts, 미국, 02115
        • Boston Children's Hospital

참여기준

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자격 기준

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아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Sickle Cell Disease
Cas9 리보핵단백질을 표적으로 하는 BCL11A 인핸서로 전기천공된 자가 골수 유래 CD34+ HSPC
제외 기준 12번에 대한 진단 테스트를 수행하는 데 사용되는 장치

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
일차생착
기간: 42일
조절 후 성공적인 조혈 재구성(성장 인자 지원 없이 3일 연속 0.5 x 10^9/L 이상의 절대 호중구 수(ANC)로 정의), 줄기 세포 주입 0일 후 42일까지 달성(즉, "1차 생착").
42일

2차 결과 측정

결과 측정
측정값 설명
기간
헤모글로빈
기간: 24개월
총 헤모글로빈(g/dL), 헤모글로빈 분율(A, F, S(g/dL)), HbF 비율, F 세포 비율
24개월
혈소판 이식
기간: 42일
혈소판 생착(줄기세포 주입 후 +42일 기준 7일 동안 수혈 없이 혈소판 수가 ≥20,000/L로 정의됨)
42일
삶의 질
기간: 24 개월
18 세 미만의 피험자에 대한 환자 (또는 어린 자녀의 부모)에게 PEDSQL 조사 도구를 투여함으로써 평가 된 삶의 질, 성인 피험자를위한 SF-36 조사 도구의 투여
24 개월
Severe vaso-occlusive crises
기간: 24 months
Change from baseline in incidence of severe vaso-occlusive crises (requiring emergency department visit or hospital admission)
24 months
Acute chest syndrome
기간: 24 months
Change from baseline in incidence of acute chest syndrome
24 months
Stroke
기간: 24 months
Change from baseline in incidence of stroke
24 months
Splenic sequestration
기간: 24 months
Change from baseline in incidence of splenic sequestration
24 months
Transfusion requirement
기간: 24 months
Change from baseline in transfusion requirement (in mL/kg) after day +100 post infusion
24 months
Reticulocyte count
기간: 24 months
Change from baseline reticulocyte count
24 months
Bilirubin
기간: 24 months
Change from baseline bilirubin
24 months
Lactate dehydrogenase (LDH)
기간: 24 months
Change from baseline lactate dehydrogenase (LDH)
24 months

기타 결과 측정

결과 측정
측정값 설명
기간
안전 결과: 사망
기간: 24개월
사망의 발생
24개월
안전성 결과: 심각한 부작용
기간: 24개월
심각한 부작용의 수
24개월
14. Safety Outcome: Malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
기간: 24 months
Occurrence of malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
24 months

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스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 8월 1일

기본 완료 (추정된)

2028년 12월 1일

연구 완료 (추정된)

2030년 12월 1일

연구 등록 날짜

최초 제출

2026년 7월 13일

QC 기준을 충족하는 최초 제출

2026년 7월 13일

처음 게시됨 (실제)

2026년 7월 16일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 16일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 13일

마지막으로 확인됨

2026년 7월 1일

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