This study is a single arm clinical study to observe the safety ,dose tolerance and pharmacokinetic characteristics of CAR NK-CD19 in patients with recurrent or refractory CD19 positive acute lymphoblastic leukemia, and preliminarily evaluate the effectiveness, the immunogenicity of the product and the correlation between the changes of cytokines after infusion and CRS , ICANS.
Age range
3 Years
Sex
ALL
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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.
Safety of CAR NK-CD19 Cell
Timeframe: Up to 3 months after cell infusion
Cell count of CAR NK-CD19
Timeframe: From 1 to 720 days after infusion
Cmax of CAR NK-CD19
Timeframe: From 1 to 720 days after infusion
Tmax of CAR NK-CD19
Timeframe: From 1 to 720 days after infusion
AUC of CAR NK-CD19
Timeframe: From 1 to 720 days after infusion
Other pharmacokinetic of CAR NK-CD19 Cell
Timeframe: From 1 to 720 days after infusion