National Institute of Hematology, Chinese Academy of Medical Sciences
Tianjin, Tianjin Municipality, 300000, China
Location status: Recruiting
NCT Number: NCT06608732
Evaluate the safety and efficacy of Inaticabtagene autoleucel combined with autologous hematopoietic stem cell transplantation in adolescents or adults with MRD-positive initial complete remission in B-cell acute lymphoblastic leukemia.
Interested in participating?
Request Info16 year–70 year
All sexes
Interventional
Phase 2
Tianjin, Tianjin Municipality, 300000, China
Location status: Recruiting
Evaluate the safety and efficacy of Inaticabtagene autoleucel combined with autologous hematopoietic stem cell transplantation in adolescents or adults with MRD-positive initial complete remission in B-cell acute lymphoblastic leukemia.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
CNCT19 combined with autologous hematopoietic stem cell transplantation,Dose: (0.5 -2)x 10^6/kg CNCT19 Cell Injection via intravenous infusion.
Time frame: From autologous hematopoietic stem cell transplantation to 2 years after transplantation
The time from the start of infusion of Inaticabtagene autoleucel until the diagnosis of relapse or any death (whichever comes first).
Time frame: From autologous hematopoietic stem cell transplantation to 2 years after transplantation
Time frame: From autologous hematopoietic stem cell transplantation to 2 years after transplantation
Time frame: 28 days after the first CAR-T cell reinfusion
Institute of Hematology & Blood Diseases Hospital, China
Other
Clinical Study of Inaticabtagene Autoleucel Combined With Autologous Hematopoietic Stem Cell Transplantation for Adolescents or Adults With MRD-Positive B-Cell Acute Lymphoblastic Leukemia in Initial Complete Remission.
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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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