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临床试验/NCT06946953
NCT06946953招募中1 期

REGEND001 Autologous Basal Layer Stem Cell Transplantation for Chronic Obstructive Pulmonary Disease (COPD): A Translational Application Study

Ruijin Hospital2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年3月23日最近更新:
干预措施

试验速览

阶段
1 期
状态
招募中
入组人数
20
试验地点
2
主要终点
Change in DLCO from baseline.

研究概览

简要总结

This clinical trial aims to evaluate the safety and efficacy of REGEND001, an autologous bronchial basal cell therapy, for the treatment of Chronic Obstructive Pulmonary Disease (COPD). COPD is a chronic respiratory condition characterized by persistent airflow limitation and impaired lung function, leading to significant morbidity and mortality worldwide. Current treatments primarily focus on symptom management and have limited impact on disease progression or survival. This study proposes a novel approach using autologous bronchial basal cells, which have demonstrated the potential to repair damaged lung tissue and improve lung function in preclinical studies. The therapy involves the collection of bronchial basal cells via bronchial brushing, followed by their expansion and reintroduction into the patient's lungs via bronchoscopic infusion. The primary objective is to assess the improvement in lung diffusion capacity (DLCO), with secondary endpoints including changes in lung ventilation function (FEV1, FVC) and quality of life (CAT score). The study will also monitor safety, including the incidence of adverse events. Eligible participants are COPD patients aged 40-80 with moderate to severe disease. The trial includes a screening phase, cell collection, transplantation, and follow-up assessments at 4 and 24 weeks post-treatment. This study represents a promising advancement in regenerative medicine for COPD, offering a potential therapeutic option that addresses the underlying structural damage in the lungs.

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
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with COPD according to the 2021 Global Initiative for Chronic Obstructive Lung Disease (GOLD);
  • Post-bronchodilator FEV1/FVC <70%;
  • DLCO ≥20% and <80% of predicted value.

排除标准

  • Pregnant, breastfeeding, or planning to become pregnant within 1 year after treatment (or male participants planning for their spouse to become pregnant);
  • Positive for syphilis (TP-Ab), HIV, hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV) antibodies;
  • Current or past history of malignancy.

研究组 & 干预措施

COPD patients

Experimental

干预措施: P63+ lung progenitors (Biological)

结局指标

主要结局

Change in DLCO from baseline.

时间窗: Baseline, 4 weeks post treatment, 24 weeks post treatment

The diffusing capacity of the lungs for carbon monoxide (DLCO) is a measurement of the gas transfer capacity of lung.

次要结局

  • Change in FEV1 from baseline.(Baseline, 4 weeks post treatment, 24 weeks post treatment)
  • Change in FVC from baseline.(Baseline, 4 weeks post treatment, 24 weeks post treatment)
  • Improvement in CAT score (symptoms, activity, and psychological status).(Baseline, 4 weeks post treatment, 24 weeks post treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jieming QU

Professor

Ruijin Hospital

研究点 (2)

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