allogeneic CAR-T therapy
/ EdiGene, Beijing Imunopharm
- LARVOL DELTA
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April 10, 2025
Glycan Shielding via Single SPPL3 Ablation Enables TCR-Sufficient Long-Lasting Allogeneic CAR-T Therapy in Patients
(ASGCT 2025)
- P1/2 | "The 3+3 dose escalation design includes lymphodepletion with fludarabine (30-50 mg/m²/d) and cyclophosphamide (500-1000 mg/m²/d) for three days (day-5 to -3), followed by escalating doses of ET-901-Athena (1×10⁶/kg, 3×10⁶/kg, 10×10⁶/kg) or ET-901-Herculas (1×10⁶/kg, 3×10⁶/kg, 6×10⁶/kg). Glycan-shielded allogeneic CAR-T cells can persist for over six months, control tumors, resist immune rejection, and avoid GvHD. These findings position SPPL3 engineering as a transformative platform for universal CAR-T therapies."
Clinical • Late-breaking abstract • Dermatology • Graft versus Host Disease • Immunology • Oncology
November 06, 2024
Changes in Glycosylation on the Cell Surface Result in Highly Potent and Long-Lasting Allogeneic CAR-T Therapy in Patients
(ASH 2024)
- "Following lymphodepletion of fludarabine (30-50 mg/m2/d) and cyclophosphamide (500-1000 mg/m2/d) for a duration of 3 days, patients receive a single-dose infusion of ET-901 at escalating doses of 1*10e6/kg, 3*10e6/kg, and 10*10e6/kg. All patients demonstrated objective responses, with significant CAR-T cell expansion, confirming the engineered cells' long-term immune privilege and activity. This represents a significant step in making allogeneic CAR T-cell therapy more viable and effective."
Clinical • Anemia • Bone Marrow Transplantation • Graft versus Host Disease • Hematological Disorders • Hematological Malignancies • Immunology • Oncology • Thrombocytopenia • B2M
April 02, 2024
Changes in Glycosylation on the Cell Surface Result in Highly Potent and Long-Lasting Allogeneic CAR-T Therapy in Patients
(ASGCT 2024)
- P1/2 | "An ongoing clinical trial (NCT06014073) with these allogeneic CAR T-cell demonstrated high anti-tumor activity and persistence for more than 3 months in first 5 evaluable R/R NHL patients (Data cut-off date is January 20, 2024), with 100% ORR and 60% CR and manageable safety profile. Our research highlights the complex immune interactions and positions GeneX engineering as a promising strategy for creating universal therapeutic cells."
Clinical • Graft versus Host Disease • Hematological Malignancies • Immunology • Oncology • Transplant Rejection • B2M
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