eligibility_summary
Eligible: adults 18–70 who can consent, receiving a first kidney transplant from a heart-beating deceased donor or an ABO-compatible, non-HLA-identical living related donor. Exclude: prior kidney transplant, HLA-identical living related donor, or donor after cardiac death.
trial_source
clinical_trials.gov from Dec 2, 2025
annotation_status
manual_review_required
ai_summary
NCT05669001 (ASCEND) tests a CNI-free regimen vs standard of care in de novo kidney transplant. Experimental: TCD601 (siplizumab), a monoclonal antibody against CD2 (biologic), depleting/modulating CD2+ T and NK cells and blocking T-cell co-stimulation/adhesion, plus belatacept, a CTLA4-Ig fusion protein (biologic) that blocks CD80/86–CD28 co-stimulation on APCs, with mycophenolic acid (small-molecule antimetabolite, IMPDH inhibitor) to curb lymphocyte proliferation, and corticosteroids (steroidal immunosuppressants, glucocorticoid receptor–mediated cytokine suppression). Comparator: ATG (polyclonal antibody, T-cell depletion) + tacrolimus (small-molecule calcineurin inhibitor, NFAT/IL‑2 blockade) + MPA + steroids. Targets: CD2, CD80/86–CD28, calcineurin–NFAT, de novo purine synthesis, glucocorticoid pathways, primary cells: T cells (and NK cells).