The goal of this open label, single-arm clinical study is to learn about the safety and efficacy of CS-101 injection in treating sickle cell disease.
CS-101 is an autologous CD34+ cell suspension, edited by in vitro base editing technology, which modifies the BCL11A binding site in HBG promoter, so that it loses the ability to bind to BCL11A, which can re-induce the production of γ-globin chain and increase the concentration of fetal hemoglobin(HbF) in the blood, compensating for the function of missing adult hemoglobin HbA to achieve clinical cure. The therapy addresses two major challenges in the current treatment of the disease: lack of matching donors and graft-versus-host diseases in allogeneic hematopoietic stem cell transplantation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
Autologous CD34+ hematopoietic stem cell suspension modified by in vitro base editing technique
The First Affiliated Hospital of Guangxi Medical University
Nanning, Guangxi, China
RECRUITINGAEs(Adverse Events) and SAEs(Serious Adverse Events) after CS-101 infusion
Frequency and severity of adverse events(AEs)as assessed by CTCAE(Common Terminology Criteria for Adverse Events)v5.0
Time frame: From signing informed consent to 24 months post-CS-206 infusion
Incidence of transplant-related mortality
Incidence of transplant-related mortality(Transplant-related mortality events defined as deaths assessed by the investigator as potentially transplant-related)
Time frame: From baseline to 100 days and 12 months post-CS-206 infusion
Time to neutrophil engraftment
Time to neutrophil engraftment is defined as first day of 3 consecutive measurements of absolute neutrophil count≥0.5×10\^9/L on three different days.
Time frame: Up to 24 months post-CS-206 infusion
Time to platelet engraftment
Time to platelet engraftment is defined as first day of 3 consecutive measurements of absolute platelet count≥20×10\^9/L on three different days and without platelet transfusion.
Time frame: Up to 24 months post-CS-206 infusion
All-cause mortality
Time frame: Up to 24 months post-CS-206 infusion
Free from severe VOCs for 12 consecutive months (VF12)
Free from severe vaso-occlusive crises (VOCs) for 12 consecutive months (VF12)
Time frame: starting 60 days after the last red blood cell transfusion up to 24 months
Free from hospitalization due to severe vaso-occlusive crises for 12 consecutive months(HF12)
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Time frame: starting 60 days after the last red blood cell transfusion up to 24 months
Free from severe VOCs for 9 consecutive months (VF9)
Free from severe vaso-occlusive crises (VOCs) for 9 consecutive months (VF9)
Time frame: starting 60 days after the last red blood cell transfusion up to 24 months
Annualized incidence of severe vaso-occlusive crises (VOC)
Time frame: starting 60 days after the last red blood cell transfusion up to 24 months
Annualized incidence of hospitalization due to severe vaso-occlusive crises
Time frame: starting 60 days after the last red blood cell transfusion
HbF (fetal hemoglobin) level in blood samples
Time frame: up to 24 months post-CS-206 infusion
Proportion of edited alleles in peripheral blood leukocytes and bone marrow cells, and persistence and chimerism kinetics evaluation
Time frame: up to 24 months post-CS-206 infusion