Union Hospital
Wuhan, Hubei, 430022, China
Location status: Recruiting
NCT Number: NCT06732492
This is a single-arm, open-label, single-center, phase I study. The primary objective is to evaluate the safety of CD7 Chimeric Antigen Receptor-T(CAR-T) therapy for patients with CD7-positive relapsed or refractory natural killer/T cell lymphoma, and to evaluate the pharmacokinetics of CD7 CAR-T in patients。
Interested in participating?
Request Info3 year–70 year
All sexes
Interventional
Phase 1
Wuhan, Hubei, 430022, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
CAR-T cells
Other names: universal CD7 CAR-T cells
Time frame: Evaluate at 4 weeks after CAR-T infusion
The proportion of patients with complete response (CR) /complete response with incomplete blood cell recovery (CRi)
Time frame: Up to 1 years after CAR-T infusion
The time from CR/CRi and PR to disease relapsed or death due to disease progression after CAR-T infusion
Time frame: Up to 1 years after CAR-T infusion
The time from first achieving CR/CRi to relapse or death
Time frame: Up to 1 years after CAR-T infusion
The time from CAR-T infusion to death due to any cause
Contact information is provided by the study sponsor or research team.
Heng Mei, Ph.D&M.D
CONTACT
Yinqiang Zhang
CONTACT
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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