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To evaluate the safety and tolerability of CD19 UCAR-T cell injection in subjects with recurrent/refractory CD19 positive B cell malignancies

To evaluate the safety and tolerability of CD19 UCAR-T cell injection in subjects with recurrent/refractory CD19 positive B cell malignancies

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039849
Enrollment
Unknown
Registered
2020-11-12
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed/refractory CD19-positive B-cell malignancies

Interventions

Sponsors

Zhongshan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) 18~70 years old (including cut-off value), no gender limit; (2) The expected survival time is not less than 2 months; (3) ECOG score 0-2 points; (4) Definitely diagnosed as CD19-positive B-cell malignant tumor (CD19+ confirmed: ALL FCM (proportion > 30%); NHL immunohistochemistry (positive)) and meet one of the following conditions: a) Those who have not achieved complete remission after standard chemotherapy, or relapse early after complete remission; b) Those who relapse after stem cell transplantation will not be affected by other treatments previously used; (5) Liver and kidney function, heart and lung function meet the following requirements: a) Creatinine is within the normal range; b) Left ventricular ejection fraction > 50%; c) Baseline blood oxygen saturation > 92%; d) Total bilirubin <= 2 times the upper limit of normal; ALT and AST <= 2.5 times the upper limit of normal; (6) Able to understand this experiment and have signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those who have graft-versus-host disease (GVHD) or need to use immunosuppressive agents; (2) Patients with malignancies other than B-cell malignancies within 5 years before screening, except for fully treated cervical carcinoma in situ, basal cell or squamous cell skin cancer, local prostate cancer after radical resection, and those after radical resection Ductal carcinoma in situ; (3) Subjects with positive hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) and peripheral blood HBV DNA titer test >= 3 x 10^2 copies/L; hepatitis C virus (HCV) antibody positive and peripheral blood HCV RNA positive; human immunodeficiency virus (HIV) antibody positive; CMV DNA test positive; syphilis test positive; (4) Any unstable systemic disease: including but not limited to unstable angina, cerebrovascular accident or transient cerebral ischemia (within 6 months before screening), myocardial infarction (within 6 months before screening), congestion Congestive heart failure (New York Heart Association [NYHA] classification >= grade III), severe arrhythmia requiring medication, liver, kidney or metabolic diseases; (5) Within 14 days before enrollment, there are active infections or uncontrollable infections requiring systemic treatment; (6) Women who are pregnant or breastfeeding, and female subjects who plan to become pregnant within 1 year after cell reinfusion, or male subjects whose partners plan to become pregnant within 1 year after cell reinfusion; (7) The central nervous system is invaded; (8) Situations deemed unsuitable by other researchers.

Design outcomes

Primary

MeasureTime frame
Dose-limiting toxicity;Immunogenicity;Overall response time;Progression-free survival;Overall survival;Changes in tumor lesions;

Countries

China

Contacts

Public ContactZiwen Guo

Zhongshan People's Hospital

zsgzw@21cn.com+86 13600342062

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026