Gene Editing For Sickle Cell Disease
- Conditions
- Interventions
- Registration Number
- NCT06506461
- Lead Sponsor
- St. Jude Children's Research Hospital
- Brief Summary
This study is being done to test the safety of a new treatment called gene editing in Sickle Cell Disease (SCD) patients and to see if a single dose of this genetically modified cellular product will increase the amount of a certain hemoglobin called fetal hemoglobin (HbF) and help reduce the symptoms of SCD.
Primary Objective
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- Detailed Description
Participants will receive a daily injection of plerixafor under the skin for 3-5 days to mobilize their hematopoietic stem and progenitor cells (HSPCs) into peripheral blood. About 2-4 hours after each dose of plerixafor is given, the collection of HSPCs will start via apheresis. The collected HSPCs will be sent to a lab to genetically modify them using CRIS...
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 25
- Age ≥18 years and ≤24.9 years.
- Patients with SCD (Hb SS, Hb SB0 and Hb SB+ genotype) who have experienced EITHER (a) 2 or more SCD-related vaso-occlusive events (acute pain events, acute chest syndrome, priapism and splenic sequestration) per year in the 2-year period before screening, OR (b) administration of regular red blood cell (RBC) transfusions (≥8 transfusions in the 12 months preceding enrollment) EXCEPT if the RBC transfusions are being administered for primary or secondary stroke prevention and, in the opinion of the treating hematologist, cannot be safely discontinued after infusion of the gene modified drug product.
- Failure, intolerance, or refusal of hydroxyurea therapy.
- Patients must be eligible for autologous stem cell transplant as per investigator's judgment.
- Females of childbearing potential (i.e., those who are post-menarchal with an intact uterus and at least 1 ovary, and those who are less than 1 year postmenopausal) must agree to use acceptable method(s) of contraception from start of mobilization through at least 6 months post-infusion.
- Males must agree to use effective contraception from start of mobilization through at least 6 months post-infusion.
- Patients should be willing to participate in an additional long-term follow-up study after completion of this trial.
- Availability of an human leukocyte antigen (HLA)-matched sibling who is willing and able to donate an appropriate graft for hematopoietic cell transplantation (HCT).
- Karnofsky or Lansky performance score < 80.
- Pregnant, as confirmed by positive serum or urine pregnancy test within 14 days before enrollment (if female).
- Breastfeeding.
- Uncontrolled (undergoing appropriate treatment and with progression of clinical symptoms) or clinically significant bacterial, viral, or fungal infections within 1 month before enrollment.
- Patients with confirmed Hepatitis B or Hepatitis C infections.
- Patients with confirmed seropositivity or positive nucleic acid amplification test (NAAT) for human immunodeficiency virus (HIV) or human T-cell lymphotropic virus (HTLV).
- Patients with a history of stroke.
- Serum conjugated (direct) bilirubin > 2× the upper limit of normal for age, or serum alanine transaminase (ALT) > 3× the upper limit of normal for age as per the local laboratory. Participants with hyperbilirubinemia or elevated aspartate aminotransferase (AST) as the result of hyperhemolysis, or with a severe drop in hemoglobin post blood transfusion, are not excluded as long as these values downtrend and return to acceptable limits subsequently.
- Left ventricular shortening fraction < 25% or ejection fraction < 45% by echocardiogram.
- Estimated creatinine clearance less than 60 mL/min/1.73m^2.
- Diffusion capacity of carbon monoxide (DLCO) < 50% (adjusted for hemoglobin) OR baseline oxygen saturation < 85% in patients unable to perform pulmonary function tests.
- Prior HCT or gene therapy.
- Known hepatic cirrhosis, bridging hepatic fibrosis, or active hepatitis. Appropriate ultrasound or magnetic resonance (MR) imaging may be used to define the presence and degree of cirrhosis. Liver biopsy may be performed at the discretion of the attending physician or principal investigator if there are concerns regarding the presence of severe hepatic fibrosis or cirrhosis such that participation in this trial will not be in the patient's best interest.
- Active known malignancy, myelodysplasia, abnormal cytogenetics, or immunodeficiency.
- Patients with history of a significant bleeding disorder.
- Cerebrovascular procedure within 6 months, including pial synangiosis for moyamoya.
- Patients with history of untreated moyamoya disease or presence of moyamoya disease at screening that in the opinion of the investigator puts the subjects at the risk of bleeding.
- Evidence of a pathogenic clonal variant in any candidate gene detected by a standard, licensed next-generation sequencing clinical assay for gene mutations associated hematological malignancies.
- Patients with history of intolerance, contraindication, or known sensitivity to plerixafor or busulfan. Prior anaphylactic reaction with excipients of the proposed product.
- Patients with participation in another clinical study with an investigational drug/product within 30 days of screening or fewer than 5 half-lives of the investigational agent whichever is longer from screening.
- Patients with history of alloimmunization to RBC antigens and for whom the investigator anticipates that there will be insufficient RBC units available for the duration of the study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Autologous, genetically modified CD34+ HSPCs Treatment Plerixafor All eligible participants receive intervention as described in the Detailed Description with the following: plerixafor, busulfan, and autologous, gene-modified CD34+ cells Autologous, genetically modified CD34+ HSPCs Treatment Busulfan All eligible participants receive intervention as described in the Detailed Description with the following: plerixafor, busulfan, and autologous, gene-modified CD34+ cells Autologous, genetically modified CD34+ HSPCs Treatment Gene-modified CD34+ cells All eligible participants receive intervention as described in the Detailed Description with the following: plerixafor, busulfan, and autologous, gene-modified CD34+ cells
- Primary Outcome Measures
Name Time Method Frequency of off-target editing after infusion of the CRISPR/Cas9-edited CD34+ HSPCs. Within 3 years of the cellular product infusion Frequency of off-target editing will be described using descriptive statistics.
Incidence of platelet engraftment by day +60 after infusion of the CRISPR/Cas9-edited CD34+ HSPCs. Within 60 days of the cellular product infusion Upon completion of the trial, summary statistics will be computed for the time to platelet engraftment.
Sustenance of multi-lineage engraftment and polyclonal hematopoiesis as measured by counts of different clones of myeloid cells, T cells, B cells, and NK cells at 1 year after infusion of the CRISPR/Cas9-edited CD34+ HSPCs. Within 1 year of the cellular product infusion Sustenance of multi-lineage engraftment will be described using descriptive statistics.
Occurrence of secondary graft failure, clonal hematopoiesis, MDS, or AML Within 3 years of the cellular product infusion Occurrence will be described using descriptive statistics.
Incidence of neutrophil engraftment by day +42 after infusion of the CRISPR/Cas9-edited CD34+ HSPCs. Within 42 days of the cellular product infusion Upon completion of the trial, summary statistics will be computed for the time to neutrophil engraftment.
- Secondary Outcome Measures
Name Time Method Compare the change from baseline in the total blood hemoglobin concentration. From time of screening to 3 years post infusion The change from baseline (at the time of screening) in the total blood hemoglobin concentration will be calculated at various timepoints as described in the protocol. The changes will be summarized using descriptive statistics and displayed graphically.
Estimate the change in the annualized rate of SCD-related vaso-occlusive events (such as pain crises and acute chest syndrome events), starting at 3 months after the infusion of autologous CRISPR/Cas9-edited CD34+ HSPCs. From 3 months post the cellular product infusion to 3 years post infusion We will evaluate the change in the annualized rate of SCD-related vaso-occlusive events starting at 3 months after the infusion of autologous gene-edited CD34+ HSPCs relative to the annualized rate calculated during the 2-year period before study enrollment. The changes will be summarized using descriptive statistics and displayed graphically.
Change in incidence of packed RBC transfusions. Within 1 year prior to infusion and within 3 months to 1 year post infusion The change from baseline (at the time of screening) in the incidence of packed RBC transfusions will be calculated at various timepoints as described in the protocol. The changes will be summarized using descriptive statistics and displayed graphically.
Compare the change from baseline in the fraction of red blood cells (RBCs) containing HbF. From time of screening to 3 years post infusion The change from baseline (at the time of screening) in the fraction of RBCs containing HbF by immunostaining will be calculated at various timepoints as described in the protocol. The changes will be summarized using descriptive statistics and displayed graphically.
Trial Locations
- Locations (1)
St. Jude Children's Research Hospital
🇺🇸Memphis, Tennessee, United States