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/ Not yet recruiting早期临床1期IIT An Exploratory Clinical Study of the Safety and Efficacy of CD19 Chimeric Antigen Receptor NK Cells for the Treatment of Refractory Antisynthetase Antibody Syndrome and Rheumatoid Arthritis
A single-center, open-label dose-escalation design to evaluate the safety and efficacy of 3 infusions of anti CD19 CAR NK cells (KN5501), as well as the expansion and persistence of KN5501 in patients with refractory antisynthetase antibody syndrome (ASyS) and rheumatoid arthritis (RA); To evaluate the ability of KN5501 to clear CD19-positive B cells in patients to determine the feasibility of KN5501 for the treatment of refractory ASyS and or RA.
/ Not yet recruiting早期临床1期IIT An Exploratory Clinical Study of the Safety and Efficacy of CD19 Chimeric Antigen Receptor NK Cell Injections for the Treatment of Refractory Primary Immune Thrombocytopenia
A single arm, open-label pilot study is designed to determine the safety and effectiveness of CD19 CAR NK cells (KN5501) in patients with refractory immune thrombocytopenia. 9 patients are planned to be enrolled in the dose-escalation trial (9×10^9 cells, 13.5×10^9 cells). The primary objective of the study is to evaluation of the safety and feasibility of KN5501 for the treatment of relapsed/refractory B-cell related autoimmune diseases. The secondary objective is to evaluate evaluation of KN5501 for the treatment of refractory immune thrombocytopenia. The exploratory objective is to evaluate expansion, persistence and ability to deplete CD19 positive B cells of KN5501 in patients with refractory immune thrombocytopenia.
An Exploratory Clinical Study of the Safety and Efficacy of CD19 Chimeric Antigen Receptor NK Cell Injection for the Treatment of Relapsed/Refractory Autoimmune Diseases
A single arm, open-label pilot study is designed to determine the safety and effectiveness of CD19 CAR NK cells in patients with autoimmune diseases. 36-72 patients are planned to be enrolled in the dose-escalation trial. The primary objective of the study was to evaluate the safety and feasibility of CD19 CAR-NK cells for the treatment of patients with autoimmune diseases. The secondary objective is to evaluate the efficacy of CD19 CAR-NK cells in patients with autoimmune diseases.
100 项与 深圳恩瑞恺诺生物技术有限公司 相关的临床结果
0 项与 深圳恩瑞恺诺生物技术有限公司 相关的专利(医药)
2024年11月14-19日,美国风湿病学会年会(ACR)在华盛顿召开,恩瑞恺诺CD19 CAR-NK疗法治疗复发性系统性红斑狼疮的最新临床数据公开发表。20例活动性重度复发性系统性红斑缆车患者接受了3个剂量的CD19 CAR-NK治疗。第一个级联组1例,第二个剂量组1例,第三个剂量组5例,第四个级联组13例。安全性方面,只观察到2例患者出现1级CRS(短暂发热),没有其他副作用和感染事件。有效性方面,对于8例随访6个月以上的患者,4例(50%)达到DORIS缓解,6例(75%)达到LLDAS(低狼疮疾病活动度)。
11月18日,CAR-NK先驱Fate Therapeutics宣布其通用CAR-T疗法FT819治疗受理狼疮患者的临床数据,该患者没有观察到3级及以上副作用,达到DORIS缓解,脱离所有免疫抑制剂治疗,重建B细胞主要是Naive、non-class switched的B细胞。
今年7月,邦耀生物在Cell期刊上发表了其通用CD19 CAR-T疗法治疗自身免疫病的临床数据。此次恩瑞恺诺发表了CD19 CAR-NK重度狼疮患者的20例临床数据,CAR-NK先驱Fate Therapeutics也宣布通用CAR-T治疗首例狼疮患者的优异疗效数据。通用CAR-T或CAR-NK或将在自免领域率先实现临床突破,期待其早日上市。
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100 项与 深圳恩瑞恺诺生物技术有限公司 相关的药物交易
100 项与 深圳恩瑞恺诺生物技术有限公司 相关的转化医学