Shanghai Changzheng Hospital
Shanghai, Shanghai Municipality, 200131, China
Location status: Recruiting
NCT Number: NCT07144462
The purpose of this study is to determine the safety, tolerability and preliminary efficacy of NEUK203-215 , a healthy donor (HD) allogeneic CD19/BCMA-targeted CAR-NK cell product, in participants with severe, refractory autoimmune diseases.
This study plans to conduct an interim data analysis when the cumulative enrollment reaches 50% of the total sample size. The objectives of this analysis are: (1) to summarize the safety and tolerability profile at the current dose level; (2) to preliminarily assess trends in clinical response endpoints and explore preliminary signals of drug efficacy; and (3) to preliminarily evaluate the pharmacokinetic and pharmacodynamic characteristics of the drug in humans. This analysis is exploratory in nature and is intended to accumulate preliminary clinical evidence for the drug in the target patient population.
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Early Phase 1
Shanghai, Shanghai Municipality, 200131, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Time frame: Up to 12 months post NEUK203-215 infusion
Time frame: Up to 12 months post NEUK203-215 infusion
Time frame: Up to 12 months post NEUK203-215 infusion
Contact information is provided by the study sponsor or research team.
Neukio Biotherapeutics (Shanghai) Co., Ltd.
Industry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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