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.
Age range
6 Years – 35 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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