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eligibility_summary
Consent, adults with relapsed/refractory B-cell lymphoma: DLBCL (NOS/transformed), FL grade 3B, PMBCL, HGBCL double/triple-hit, or adult FL refractory >=2L or relapsed <=24 mo. Prior relmacabtagene autoleucel with assessment, retreatment planned, adequate product, CD19+ tumor if feasible, no ADA, lymphodepletion tox resolved to <=G1, prior AEs resolved. Exclude: hypersensitivity (incl DMSO/HSA) or uncontrolled infection.
trial_source
clinical_trials.gov from Dec 2, 2025
annotation_status
ai
ai_summary
Phase 4, single-arm trial testing a secondary infusion of relmacabtagene autoleucel (CARTEYVA), an autologous, gene‑modified CD19-directed CAR‑T cell therapy, in adults with relapsed/refractory B‑cell lymphoma who failed to achieve complete remission after the first infusion. Mechanism: patient T cells are engineered to express an anti‑CD19 CAR with 4‑1BB costimulatory and CD3ζ signaling domains, upon binding CD19, CAR‑T cells expand and kill malignant B cells via perforin/granzyme-mediated cytotoxicity, leading to B‑cell depletion. Targets/pathways: CD19 on B‑cell lymphomas, T‑cell activation and persistence via 4‑1BB/CD3ζ signaling, aiming to overcome inadequate expansion/persistence or functional exhaustion.