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Effect of chimeric antigen receptor T cells followed by allogeneic hematopoietic stem cell transplantation for relapsed/refractory acute lymphoblast leukemia: A phase II, unblind, uncotroll clincial trial in a single center

Effect of chimeric antigen receptor T cells followed by allogeneic hematopoietic stem cell transplantation for relapsed/refractory acute lymphoblast leukemia: A phase II, unblind, uncotroll clincial trial in a single center

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-16008448
Enrollment
Unknown
Registered
2016-05-09
Start date
2016-04-10
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

relapsed/refractory acute lymphoblast leukemia

Interventions

experimental group:Chimeric antigen receptor T cells followed by allogeneic hematopoietic stem cell transplantation

Sponsors

Department of Hematology, Xinqiao Hospital, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 55 Years

Inclusion criteria

Inclusion criteria: 1) Male or Female; Aged below 55 years; 2) Refractory/relapsed acute lymphoblast leukemia with CD19 expression and no other effectvie way to select; 3) The estimated survial is over three months; 4) ECOG performance status of <=2 at study entry; 5) The important organs are function, such as heart and brain; 6)Understand and voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1) The uncontrol infetion, HBV and HCV are positive; 2) The patients received any cell immunotherapy in the past.

Design outcomes

Primary

MeasureTime frame
One-year disease-free survival;

Secondary

MeasureTime frame
Overall Survival;The Rate of graft-versus-host disease;The rate of infection;

Countries

China

Contacts

Public ContactZhang Cheng

Department of Hematology, Xinqiao Hospital, Third Military Medical University

chzhang2014@163.com+86 13098770350

Outcome results

None listed

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