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临床试验/NCT07592754
NCT07592754尚未招募1 期

An Early Exploratory Clinical Study on the Safety and Efficacy of KSVCBD Injection in the Treatment of Relapsed/Refractory AQP4 Antibody-Positive Neuromyelitis Optica Spectrum Disorder.

Chinese PLA General Hospital1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2026年5月15日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
18
试验地点
1

研究概览

简要总结

KSVCBD injection is an in vivo Chimeric Antigen Receptor T-Cell (CAR-T cell) therapy product. This is a multi-center, single-arm, open-label, early exploratory clinical study. The objective of this study is to evaluate the safety and preliminary efficacy of KSVCBD injection in AQP4-positive Neuromyelitis Optica Spectrum Disorder

详细描述

KSVCBD-R103 is an open-label study in subjects with NMOSD. The dose-escalation will be conducted to evaluate the safety and preliminary efficacy of KSVCBD. This study consists of a screening period, a treatment period and a follow-up period. During treatment period, the subjects will receive single-dose of KSVCBD injection. The duration of participation for each subject will be approximately 104 weeks.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must meet the 2015 International Consensus Diagnostic Criteria for Neuromyelitis Optica Spectrum Disorder (NMOSD) and test positive for AQP4 antibodies.
  • Documented evidence of at least 1 relapse within 12 months before signing the informed consent form.
  • The Expanded Disability Status Scale (EDSS) score ≤
  • Female participants of childbearing potential must present a negative pregnancy test at screening and agree to use effective contraception throughout the study period.
  • Informed consent must be obtained from the patient or their legal representative, with a signed consent form must be provided.

排除标准

  • Viral infections: Known HIV, active HBV, or active HCV.
  • Pregnant or breastfeeding women.
  • History of other autoimmune diseases requiring immunosuppressive therapy.
  • Use of any live vaccines against infectious disease within 6 weeks before enrollment.
  • History of bone marrow/hematopoietic stem cell or solid organ transplantation.
  • Patients deemed unsuitable for participation by the investigator.

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Shihui Wei

Chief Physician and Professor

Chinese PLA General Hospital

研究点 (1)

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