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Study identifier: NCT07570563 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Clinical Study of the Safety and Efficacy of Allogeneic TCR-enhanced Vδ2 T Cell in Patients With Malignant Tumors.

Condition: Hematologic Malignancy · Solid Tumor  ·  Sponsor: Chinese PLA General Hospital

PhasePhase 1/Phase 2
Planned participants24
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The allogeneic TCR-enhanced Vδ2 T cell product is a novel genetically engineered cellular therapeutic. By engineering a specific BTN protein-binding moiety on its cell surface, this product harnesses the intrinsic tumoricidal potential of endogenous Vδ2 T cells and augments BTN protein recognition capability, thereby significantly boosting tumor cell killing potency. Notably, this engineered cell product exhibits no expression of co-stimulatory signaling domains and CD3ζ domains. This design circumvents T cell exhaustion triggered by overactivation and markedly enhances the in vivo persistence of therapeutic cells. This is an open, prospective, open-label Phase I/II clinical trial designed to assess the safety and therapeutic efficacy of allogeneic TCR-enhanced Vδ2 T cell injection in patients with relapsed or refractory hematologic malignancies and advanced solid tumors.

This description comes directly from the study's public registry record.

Talk to the study team

Weidong Han  ·  +86-010-55499341  ·  hanwdrsw@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Biotherapeutic Department of Chinsese PLA Gereral HospitalBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07570563