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Clinical Study of Universal CAR-γδT Cell Injection in the Treatment of Patients With Relapsed AML After Transplantation

Clinical Study of Universal CAR-γδT Cell Injection in the Treatment of Patients With Relapsed AML After Transplantation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04796441
Enrollment
20
Registered
2021-03-12
Start date
2020-12-16
Completion date
2022-02-16
Last updated
2021-03-12

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

Conditions

AML

Keywords

AML γδT CAR-

Brief summary

This is an open single-arm clinical study aimed at evaluating the efficacy and safety of universal γδT cell injection in the treatment of patients with relapsed AML after transplantation

Detailed description

Main purpose: To evaluate the safety and effectiveness of universal CAR-γδT cell injection in the treatment of patients with relapsed AML after transplantation Secondary purpose: to investigate the in vivo dynamics characteristics of universal CAR-γδT cells after infusion and explore reasonable therapeutic doses through climbing tests in different dose groups.

Interventions

BIOLOGICALCAR-γδT

Biological: CAR-γδT; Drug: Cyclophosphamide,Fludarabine; Procedure: Leukapheresis;

Sponsors

Hebei Senlang Biotechnology Inc., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
2 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Patients with clinically diagnosed recurrence of AML after receiving transplant therapy; 2. Flow cytometry (FCM) or immunohistochemical detection of tumor cells confirmed CD123 positive; 3. Age ≥2 years old and \<65 years old; 4. Survival is expected to be greater than 3 months from the date of signing of the informed consent; 5. KPS 80 points or more; 6. The functions of vital organs shall meet the following conditions: 1\) EF\>50%, and no obvious ECG abnormality; 2) SpO2 90% or more; 3) Cr 2.5 ULN or less; 4) ALT And AST≤5ULN, TBil≤3ULN; 7. Subjects who plan to become pregnant must agree before study enrollment and after study duration of 6 months Use contraception; Inform the investigator immediately if the subject is pregnant or suspected to be pregnant; 8. Subject or guardian understands and signs the informed consent;

Exclusion criteria

* 1\. Other diseases that have not been effectively controlled, including but not limited to persistent or poorly controlled infections and diseases Congestive heart failure, unstable angina pectoris, arrhythmias, poorly controlled lung disease Or mental illness; 2. Other active malignant tumors; 3. Complicated with severe infection that cannot be effectively controlled; 4. Active hepatitis B (HBVDNA) or HCV RNA \[HCVRNA\] test was positive); 5. Human immunodeficiency virus (HIV) infection or syphilis infection; 6. Have a history of severe allergy to biological products (including antibiotics); 7. Acute graft-versus-host reaction (GVHD) was still present one month after discontinuation of immunosuppressant therapy Allogeneic hematopoietic stem cell transplantation patients; 8. Female subjects are in pregnancy and lactation; 9. Active autoimmune diseases requiring systemic immunosuppression; 10. Conditions that the investigator believes may increase the risk of the subject or interfere with the results of the test;

Design outcomes

Primary

MeasureTime frameDescription
Safety: Incidence and severity of adverse eventsFirst 1 month post CAR-T cells infusionTo evaluate the possible adverse events occurred within first one month after CAR-γδT infusion, including the incidence and severity of symptoms such as cytokine release syndrome and neurotoxicity
Efficacy: Remission Rate3 months post CAR-T cells infusionRemission Rate including complete remission(CR)、CR with incomplete blood count recovery(CRi)、No remission(NR)

Secondary

MeasureTime frameDescription
duration of response (DOR)24 months post CAR-T cells infusionduration of response (DOR)
Efficacy: progression-free survival (PFS)24 months post CAR-T cells infusionprogression-free survival (PFS) time
CAR-T proliferation3 months post CAR-T cells infusionthe copy number of CAR- γδT cells in the genomes of PBMC by qPCR method
Cytokine releaseFirst 1 month post CAR-T cells infusionCytokine( IL-6,IL-10,IFN-γ,TNF-α ) concentration (pg/mL) by flow cytometry method

Countries

China

Contacts

Primary ContactPeihua MD Lu, PhD
peihua_lu@126.com008618611636172
Backup ContactJianqiang MD Li, PhD
limmune@gmail.com008615511369555

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026