About this trial
This clinical trial is a non-interventional, observational, multicenter, post-marketing real-world study to evaluate the efficacy and safety of Inaticabtagene Autoleucel Injection in Chinese adult patients with relapsed or refractory B-cell acute lymphoblastic leukemia.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥ 18 years;
Diagnosed with relapsed or refractory B-cell acute lymphoblastic leukemia;
Patients deemed eligible for receiving commercial Inaticabtagene Autoleucel injection treatment as determined by the investigator;
Patients voluntarily participate in this study and sign an informed consent form. For patients lacking full legal capacity, informed consent must be obtained from their legal guardian
Disqualifiers
None
Trial population
Diagnosed with adult relapsed or refractory B-cell acute lymphoblastic leukemia.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
overall survival
OS is defined as the time from the start date of Inaticabtagene Autoleucel Injection infusion to the date of death due to any cause.
Sponsors and contacts
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