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临床试验/NCT06608719
NCT06608719已完成不适用

Retrospective Study on the Safety and Therapeutic/Improvement Effects of Intravenous Administration of SHED-CM for ALS

Hitonowa Medical1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年12月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
24
试验地点
1
主要终点
All Adverse Events

研究概览

简要总结

In this study, we will retrospectively evaluate the safety and efficacy of administering SHED-CM for the treatment of ALS.

详细描述

Amyotrophic Lateral Sclerosis (ALS) is a progressive and irreversible neurodegenerative disease with limited treatment options. Advances in regenerative medicine have opened new avenues for therapeutic interventions. This retrospective cohort study evaluated the safety and efficacy of stem cells from human exfoliated deciduous teeth-conditioned media (SHED-CM) in 24 patients with ALS treated at a single facility between January 1, 2022, and November 30, 2023. Safety assessments included adverse events, vital signs, and laboratory test changes before and after administration, whereas efficacy was measured using the ALS Functional Rating Scale-Revised (ALSFRS-R), grip strength, and forced vital capacity. while ALSFRS-R scores typically decline over time, the progression rate in this cohort was slower, suggesting a potential delay in disease progression. Alternatively, improvements in muscle strength and mobility were observed in some patients. Although adverse events were reported in only 3% of cases (no serious allergic reactions), the treatment-induced changes in vital signs and laboratory results were not clinically significant. The SHED-CM treatment appears to be a safe and potentially effective therapeutic option for patients with ALS. Further research is needed to optimize the SHED-CM treatment; however, this study lays the groundwork for future exploration of regenerative therapies for ALS.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
38 Years 至 81 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients who visited our clinic between January 1, 2022 and November 30, 2023 and have been diagnosed with ALS
  • male and female patients aged between 16 and 90 years old
  • ALSFRS-R score of 12 or more at the time of initial visit

排除标准

  • Patients who have a tracheostomy at the time of visit.
  • Patients who have expressed their refusal to participate in this study.

研究组 & 干预措施

Receiving the study drug

Patients diagnosed with ALS who visited our hospital and were administered SHED-CM between January 1, 2022, and November 30, 2023.

干预措施: The study drug is SHED-CM manufactured by U-Factor (Biological)

结局指标

主要结局

All Adverse Events

时间窗: after the treatment

This measure will check the total number of adverse events (AEs) reported during the study, categorized by CTCAE Ver 5.0 .

Number of Clinically Significant Changes in Laboratory Test Results

时间窗: Baseline (pre-treatment) and after 4th treatment

This measure will track the number of events where clinically significant abnormalities are detected in laboratory test parameters, including blood count, biochemistry, and coagulation function tests. Changes from baseline to after the 4th treatment session will be evaluated based on predefined clinical thresholds.

Number of Clinically Significant Changes in Vital Signs

时间窗: Baseline (pre-treatment), post-treatment, and after 4th treatment

This measure will evaluate the number of events where clinically significant changes in vital signs occur. Parameters include systolic blood pressure, diastolic blood pressure, pulse rate, body temperature, and SpO2. Each event will be assessed at two time points: immediately after treatment and after the 4th treatment session, comparing values to baseline.

Safety assessment during the study period: Adverse events - Self- and other findings

时间窗: after the treatment

Medical examination, subjective findings, Other findings

次要结局

  • Efficacy assessment: Changes in grip strength(Change from baseline at 16 weeks)
  • Efficacy assessment: Changes in Amyotrophic Lateral Sclerosis Functional Rating Scale Revised version(Change from baseline at 16 weeks)
  • Efficacy assessment: Changes in %FVC(Change from baseline at 16 weeks)

研究者

发起方
Hitonowa Medical
申办方类型
Other
责任方
Sponsor

研究点 (1)

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