- ICH GCP
- Registre américain des essais cliniques
- Essai clinique 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.
Aperçu de l'étude
Statut
Les conditions
Description détaillée
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.
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Emily Morris
- Numéro de téléphone: 631-355-8724
- E-mail: gene.therapy@childrens.harvard.edu
Lieux d'étude
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Massachusetts
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Boston, Massachusetts, États-Unis, 02115
- Boston Children's Hospital
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
Accepte les volontaires sains
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Sickle Cell Disease
|
HSPC CD34+ autologues dérivées de la moelle osseuse électroporées avec un amplificateur BCL11A ciblant la ribonucléoprotéine Cas9
Dispositif utilisé pour réaliser les tests de diagnostic du critère d'exclusion numéro 12
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Greffe primaire
Délai: 42 jours
|
Reconstitution hématopoïétique réussie après conditionnement (définie par un nombre absolu de neutrophiles (ANC) supérieur ou égal à 0,5 x 10 ^ 9 / L pendant trois jours consécutifs sans facteur de croissance), obtenue au jour 42 après le jour 0 de la perfusion de cellules souches (c.-à-d. "greffe primaire").
|
42 jours
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Hémoglobine
Délai: 24 mois
|
Hémoglobine totale (en g/dL), fractions d'hémoglobine (A, F et S en g/dL), pourcentage d'HbF et pourcentage de cellules F
|
24 mois
|
|
Greffe de plaquettes
Délai: 42 jours
|
Greffe de plaquettes (définie comme une numération plaquettaire ≥ 20 000/L sans transfusion pendant 7 jours par jour +42 après la perfusion de cellules souches)
|
42 jours
|
|
Qualité de vie
Délai: 24 mois
|
Qualité de vie, évaluée par l'administration de l'outil d'enquête PEDSQL au patient (ou parents de jeunes enfants) pour les sujets de moins de 18 ans et par l'administration de l'outil d'enquête SF-36 pour les sujets adultes
|
24 mois
|
|
Severe vaso-occlusive crises
Délai: 24 months
|
Change from baseline in incidence of severe vaso-occlusive crises (requiring emergency department visit or hospital admission)
|
24 months
|
|
Acute chest syndrome
Délai: 24 months
|
Change from baseline in incidence of acute chest syndrome
|
24 months
|
|
Stroke
Délai: 24 months
|
Change from baseline in incidence of stroke
|
24 months
|
|
Splenic sequestration
Délai: 24 months
|
Change from baseline in incidence of splenic sequestration
|
24 months
|
|
Transfusion requirement
Délai: 24 months
|
Change from baseline in transfusion requirement (in mL/kg) after day +100 post infusion
|
24 months
|
|
Reticulocyte count
Délai: 24 months
|
Change from baseline reticulocyte count
|
24 months
|
|
Bilirubin
Délai: 24 months
|
Change from baseline bilirubin
|
24 months
|
|
Lactate dehydrogenase (LDH)
Délai: 24 months
|
Change from baseline lactate dehydrogenase (LDH)
|
24 months
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Résultat en matière de sécurité : décès
Délai: 24 mois
|
Survenance du décès
|
24 mois
|
|
Résultat en matière de sécurité : événements indésirables graves
Délai: 24 mois
|
Nombre d'événements indésirables graves
|
24 mois
|
|
14. Safety Outcome: Malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
Délai: 24 months
|
Occurrence of malignancy, abnormal bone marrow cytogenetics, or myelodysplasia
|
24 months
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Maladies génétiques, innées
- Maladies hématologiques
- Anémie, hémolytique, congénitale
- Anémie, hémolytique
- Anémie
- Hémoglobinopathies
- Maladies et anomalies congénitales, héréditaires et néonatales
- Maladies hémiques et lymphatiques
- Anémie, Drépanocytose
- Techniques d'investigation
- Techniques génétiques
- Analyse de séquence
Autres numéros d'identification d'étude
- BCH-202
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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