BENITIONSClinical Trial Intelligence

Safety & Tolerability Study of Chimeric Antigen Receptor T-Reg Cell Therapy in Living Donor Renal Transplant Recipients

1/2期 已完成 NCT04817774

适应症Kidney Transplant Rejection, End Stage Renal Disease
分期1/2期
申办方Sangamo Therapeutics
状态已完成
受试者人数26 人
干预(药物)TX200-TR101
开始日期2021年3月17日
完成日期2024年7月11日
结果公布日2026年7月2日

摘要

The purpose of this study is to evaluate the safety and tolerability of TX200-TR101 and its effects on the donated kidney in living donor kidney transplant recipients. TX200-TR101 is a product made from a kidney transplant recipient's own immune cells, which are genetically modified and designed to help the transplant recipient's body accept their donated kidney and prevent their immune system from rejecting it.

Short Term Safety and Tolerability of TX200-TR101 Infusion.

28 days post infusion · Participants

Treatment With TX200-TR101 (DL1)1 Participants
Treatment With TX200-TR101 (DL2)0 Participants
Treatment With TX200-TR101 (DL3)0 Participants
Treatment With TX200-TR101 (DL4)1 Participants
Controls2 Participants
Donors0 Participants

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。