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NCT06355739Recruiting

CD19-targeted CAR T Cell Autotransfusion for the Treatment of Recurrent/Refractory B-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma in Children With CD19+

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

Source: ClinicalTrials.gov · Last updated 9 Apr 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
2 Feb 2024
Start date
1 Feb 2024
Primary completion date
1 Dec 2026
Lead sponsor
Zhu Xiaofan
NCT number
NCT06355739

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 1 Feb 2024 to the primary completion date, 1 Dec 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • 1, severe cardiac insufficiency, left ventricular ejection fraction \<50%;
    • 2, have a history of severe lung function impairment;
    • 3\. Combined with other advanced malignant tumors;
    • 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;
    • 8\. Have a history of severe allergy to biological products (including antibiotics);
    • 9\. Patients with allogeneic hematopoietic stem cell transplantation still had acute graft-versus-host response (GvHD) one month after immunosuppressant discontinuation;
    • 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.

Who the study is looking for

  • 1, age 3-18 years old (including boundary value), male and female;
  • 2\. The patient was clinically diagnosed as relapsed/refractory B acute lymphoblastic leukemia/lymphoblastic lymphoblastic
  • Patients with tumors who meet one of the following conditions:
  • Complete marrow response (MRD\>1%) or not achieved after at least 2 courses of standardized induction regimen chemotherapy
    • 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);
  • Recurrence during chemotherapy, early recurrence after drug withdrawal (\<12 months) or late recurrence after complete remission (≥
    • 12 months) and did not achieve complete remission after 1 course of standard induction regimen (MRD\>1%);
  • Recurrence after bone marrow transplantation;
  • Simple bone marrow, simple extramedullary (testicular leukemia, central nervous system leukemia) or combined
    • recrudescence
    • 3\. Lansky score ≥60;
    • 4, the treatment related antigen test result is positive (CD19/CD20/CD22);
    • 5\. The expected survival period from the signing date of the informed consent is more than 3 months;
    • 6, HGB≥70g/L (blood transfusion);
    • 7, liver and kidney function, cardiopulmonary function meet the following requirements:
  • Creatinine ≤1.5×ULN;
  • Left ventricular ejection fraction ≥50%;
  • Blood oxygen saturation \>90%;
  • Total bilirubin ≤1.5×ULN; ALT and AST≤2.5 x ULN.-

Age in the registry: 3 years to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
InstituteHBDH
Coordinator of this site? Confirm its status
TianjinChinaNot yet recruiting
Department of Pediatrics, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences
Coordinator of this site? Confirm its status
TianjinChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.