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To evaluate the safety of general-purpose CAR-γδT cells in patients with refractory post-transplant relapsed AML.
Full description
To evaluate the efficacy and in vivo dynamics of general-purpose CAR-γδT cells in the treatment of refractory relapsed AML patients, and to explore the appropriate therapeutic dose and delivery mode.
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Inclusion criteria
The clinical diagnosis was difficult to treat recurrent acute myeloid leukemia;
Flow cytometry (FCM) or immunohistochemistry of tumor~ cells confirmed positive expression of CD123;
18 years old ≤ age ≤70 years old;
The expected survival from the date of informed consent is more than 3 months;
ECOG≤2;
The functions of vital organs shall meet the following conditions:
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;
Subject or guardian understands and signs the informed consent.
Exclusion criteria
Primary purpose
Allocation
Interventional model
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30 participants in 1 patient group
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Central trial contact
Liang Huang, PhD; Jianqiang Li, PhD
Data sourced from clinicaltrials.gov
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