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- Ensaio Clínico NCT07708350
Hematopoietic Stem Cell BCL11A Enhancer Gene Editing for Sickle Cell Disease
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.
Visão geral do estudo
Status
Descrição detalhada
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 estudo
Inscrição (Estimado)
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: Emily Morris
- Número de telefone: 631-355-8724
- E-mail: gene.therapy@childrens.harvard.edu
Locais de estudo
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Massachusetts
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Boston, Massachusetts, Estados Unidos, 02115
- Boston Children's Hospital
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Diagnosis of either a) sickle cell disease with genotype HbSS, HbS/B0 thalassemia, HbSD, or HbSO
- Age 13-40 years.
- 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.
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
Adequate organ function and performance status:
- Karnofsky performance status ≥70%
- Serum creatinine </=1.5 times the upper limit of normal for age, and calculated creatinine clearance or GFR </= 60 mL/min/1.73 m2.
- Direct bilirubin ≤ 2.0 mg/dL
- DLCO (corrected for hemoglobin), FEV1, FVC >50% of predicted
- Left ventricular ejection fraction >40% or shortening fraction >25%
- 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.
- Confirmed sickle cell disease diagnosis by molecular genetic testing.
- No HLA genotypically-identical related appropriate bone marrow donor available.
- Parental/guardian/patient signed informed consent.
- Willingness to return for follow-up for 15 years.
Exclusion Criteria:
Subjects who have concomitant condition or illness including, but not limited to:
- Uncontrolled infection, such as current febrile illness, infection requiring parenteral antibiotics, or systemic fungal infection.
- Active malignancy.
- Active complication of underlying hemoglobinopathy that would place the patient at unacceptable risk for participation, in the judgment of the Investigators.
- Major surgery in the past 30 days.
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:
- Severe cerebral vasculopathy (defined by occlusion or stenosis in the circle of Willis; or presence of Moyamoya disease)
- 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.)
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.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Sickle Cell Disease
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HSPCs CD34 + derivados de medula óssea autóloga eletroporados com intensificador BCL11A visando a ribonucleoproteína Cas9
Dispositivo utilizado para realizar os testes diagnósticos para critérios de exclusão número 12
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Enxerto primário
Prazo: 42 dias
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Reconstituição hematopoiética bem-sucedida após condicionamento (definida pela contagem absoluta de neutrófilos (ANC) maior ou igual a 0,5 x 10^9/L por três dias consecutivos sem suporte de fator de crescimento), alcançada no dia 42 após o dia 0 da infusão de células-tronco (ou seja, "enxerto primário").
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42 dias
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Hemoglobina
Prazo: 24 meses
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Hemoglobina total (em g/dL), frações de hemoglobina (A, F e S em g/dL), porcentagem de HbF e porcentagem de células F
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24 meses
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Enxerto de Plaquetas
Prazo: 42 dias
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Enxerto de plaquetas (definido como contagem de plaquetas ≥20.000/L sem transfusão durante 7 dias por dia +42 após infusão de células-tronco)
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42 dias
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Qualidade de vida
Prazo: 24 meses
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Qualidade de vida, avaliada pela administração da ferramenta de pesquisa PEDSQL para o paciente (ou pais de crianças pequenas) para indivíduos com menos de 18 anos e pela administração da ferramenta de pesquisa SF-36 para indivíduos adultos
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24 meses
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Severe vaso-occlusive crises
Prazo: 24 months
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Change from baseline in incidence of severe vaso-occlusive crises (requiring emergency department visit or hospital admission)
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24 months
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Acute chest syndrome
Prazo: 24 months
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Change from baseline in incidence of acute chest syndrome
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24 months
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Stroke
Prazo: 24 months
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Change from baseline in incidence of stroke
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24 months
|
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Splenic sequestration
Prazo: 24 months
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Change from baseline in incidence of splenic sequestration
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24 months
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Transfusion requirement
Prazo: 24 months
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Change from baseline in transfusion requirement (in mL/kg) after day +100 post infusion
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24 months
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Reticulocyte count
Prazo: 24 months
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Change from baseline reticulocyte count
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24 months
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Bilirubin
Prazo: 24 months
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Change from baseline bilirubin
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24 months
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Lactate dehydrogenase (LDH)
Prazo: 24 months
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Change from baseline lactate dehydrogenase (LDH)
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24 months
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Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Resultado de segurança: morte
Prazo: 24 meses
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Ocorrência de morte
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24 meses
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Resultado de segurança: eventos adversos graves
Prazo: 24 meses
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Número de eventos adversos graves
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24 meses
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14. Safety Outcome: Malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
Prazo: 24 months
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Occurrence of malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
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24 months
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Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- BCH-202
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