The goal of this open label, single-arm clinical study is to learn about the safety and efficacy of CS-101 in treating β-thalassemia.
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Frequency and severity of adverse events(AEs)as assessed by CTCAE v5.0
Timeframe: From signing informed consent to 12 months post-CS-101 infusion
Time to neutrophil and platelet engraftment
Timeframe: Days post-CS-101 infusion
Proportion of subjects with engraftment
Timeframe: within 42 days post-CS-101infusion
Incidence of transplant-related mortality
Timeframe: From baseline to 100 days post-CS-101 infusion
All-cause mortality
Timeframe: From signing informed consent to 12 months post-CS-101 infusion
Proportion of subjects achieving transfusion independence for at least 6 consecutive months
Timeframe: From 3 months up to 12 months post-CS-101 infusion
Time to last red blood cell(RBC) transfusion
Timeframe: Days post-CS-101 infusion