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Clinical study of CAR-T immune cell targeted therapy for recurrent/refractory leukemia and lymphoma

Clinical study of CAR-T immune cell targeted therapy for recurrent/refractory CD19+ leukemia and lymphoma

Status
Recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-17013081
Enrollment
Unknown
Registered
2017-10-23
Start date
2017-11-30
Completion date
Unknown
Last updated
2017-11-06

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

Conditions

Recurrence / refractory CD19 + leukemia, lymphoma

Interventions

Case series:Pretreated with cyclophosphamide
Infusion with 1-5×10^6 CAR-T(+) cell/kg by I.V.

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Aged between 18-75 years old male or female; 2) Diagnosed with CD19 + B cell malignancy and no other effective treatment options (such as autologous or allogeneic stem cell transfusion); 3) the use of the current treatment of poor prognosis (= 12 weeks to <2 years of survival).;Inclusion criteria: 1) Aged between 18-75 years old male or female; 2) Diagnosed with CD19 + B cell malignancy and no other effective treatment options (such as autologous or allogeneic stem cell transfusion); 3) the use of the current treatment of poor prognosis (= 12 weeks to <2 years of survival).;Inclusion criteria: 1) Aged between 18-75 years old male or female; 2) Diagnosed with CD19 + B cell malignancy and no other effective treatment options (such as autologous or allogeneic stem cell transfusion); 3) the use of the current treatment of poor prognosis (= 12 weeks to <2 years of survival).;Inclusion criteria: 1) Aged between 18-75 years old male or female; 2) Diagnosed with CD19 + B cell malignancy and no other effective treatment options (such as autologous or allogeneic stem cell transfusion); 3) the use of the current treatment of poor prognosis (= 12 weeks to <2 years of survival).;Inclusion criteria: 1) Aged between 18-75 years old male or female; 2) Diagnosed with CD19 + B cell malignancy and no other effective treatment options (such as autologous or allogeneic stem cell transfusion); 3) the use of the current treatment of poor prognosis (= 12 weeks to <2 years of survival).

Exclusion criteria

Exclusion criteria: 1) Pregnant or lactating women; 2) uncontrolled positive infection, including but not limited to hepatitis B, hepatitis C, syphilis, AIDS positive and active; 3) Use systemic steroids; 4) Previously received any other gene therapy.;Exclusion criteria: 1) Pregnant or lactating women; 2) uncontrolled positive infection, including but not limited to hepatitis B, hepatitis C, syphilis, AIDS positive and active; 3) Use systemic steroids; 4) Previously received any other gene therapy.;Exclusion criteria: 1) Pregnant or lactating women; 2) uncontrolled positive infection, including but not limited to hepatitis B, hepatitis C, syphilis, AIDS positive and active; 3) Use systemic steroids; 4) Previously received any other gene therapy.;Exclusion criteria: 1) Pregnant or lactating women; 2) uncontrolled positive infection, including but not limited to hepatitis B, hepatitis C, syphilis, AIDS positive and active; 3) Use systemic steroids; 4) Previously received any other gene therapy.;Exclusion criteria: 1) Pregnant or lactating women; 2) uncontrolled positive infection, including but not limited to hepatitis B, hepatitis C, syphilis, AIDS positive and active; 3) Use systemic steroids; 4) Previously received any other gene therapy.

Design outcomes

Primary

MeasureTime frame
Cytokine release;CAR-T proliferation;Bone marrow examination;

Countries

China

Contacts

Public ContactXuejun Zhu;Xuejun Zhu;Xuejun Zhu;Xuejun Zhu;Xuejun Zhu ;;;;

Affiliated Hospital of Nanjing University of Chinese Medicine;Affiliated Hospital of Nanjing University of Chinese Medicine;Affiliated Hospital of Nanjing University of Chinese Medicine;Affiliated Hospital of Nanjing University of Chinese Medicine;Affiliated Hospital of Nanjing University of Chinese Medicine

zhuxj2@hotmail.com;zhuxj2@hotmail.com;zhuxj2@hotmail.com;zhuxj2@hotmail.com;zhuxj2@hotmail.com+86 13505152806;+86 13505152806;+86 13505152806;+86 13505152806;+86 13505152806

Outcome results

None listed

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