CAR T cell injection
Deviceintravenous injection
NCT Number: NCT06355739
To evaluate the safety and efficacy of BIC-19GG, BIC-2019, BIC-2219 in the treatment of relapsed/refractory B acute lymphoblastic leukemia/lymphoblastic lymphoma in children
Interested in participating?
Request Info3 year–18 year
All sexes
Interventional
Not applicable
Department of Pediatrics, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences, Tianjin, Tianjin Municipality, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
1, age 3-18 years old (including boundary value), male and female;
Patients with tumors who meet one of the following conditions:
Complete response at the molecular level and immunology (characterized by specific molecular markers and immunophenotypes prior to treatment)
Patients, did not turn negative after treatment);
12 months) and did not achieve complete remission after 1 course of standard induction regimen (MRD>1%);
recrudescence
4, the treatment related antigen test result is positive (CD19/CD20/CD22);
6, HGB≥70g/L (blood transfusion);
7, liver and kidney function, cardiopulmonary function meet the following requirements:
Exclusion criteria
2, have a history of severe lung function impairment;
4, combined with serious infection and can not be effectively controlled;
5, combined with serious autoimmune disease or congenital immune deficiency;
6, active hepatitis (hepatitis B virus deoxyribonucleic acid [HBVDNA] or hepatitis C virus ribonucleic acid [HCVRNA] positive);
7, human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS), or syphilis infection;
10, the presence of other serious physical or mental illnesses or abnormalities in laboratory tests that may increase the risk of participating in the study or interfere with the study results, as well as patients deemed unsuitable for participation in the study by the investigator.
intravenous injection
Time frame: 24 months post CAR-T cell infusion
The prognosis of ALL children who underwent CAR-T cell therapy
Time frame: One month post CAR-T cell infusion
The ORR of ALL children who underwent CAR-T cell therapy
Time frame: 12 months post CAR-T cell infusion
Incidence of adverse events and its severity
Zhu Xiaofan
Other
Phase II Clinical Study on the Safety and Efficacy of Autotransfusion Agents Targeting CD19 Chimeric Antigen Receptor T Lymphocytes (BIC-19GG, BIC-2019,BIC-2219)in the Treatment of CD19-positive Children With Relapsed/Refractory B-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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