Shenzhen Geno-immune Medical Institute
Shenzhen, Guangdong, 518000, China
Location status: Recruiting
NCT Number: NCT07477600
The primary objectives are to evaluate the safety and efficacy of infusion of fully characterized clonally derived fetal mesenchymal stem cells (cfMSCs) for the control of severe symptoms associated with moderate to severe chronic obstructive pulmonary disease.
Interested in participating?
Request Info40 year–80 year
All sexes
Interventional
Phase 1 / Phase 2
Shenzhen, Guangdong, 518000, China
Location status: Recruiting
Chronic obstructive pulmonary disease (COPD) is a chronic airway inflammatory disease characterized by persistent airflow limitation, with high morbidity, disability and mortality worldwide. Traditional therapeutic methods such as bronchodilators and anti-inflammatory drugs can only relieve clinical symptoms, delay disease progression, but cannot repair the damaged alveolar and airway tissue structure, so the long-term prognosis is poor.
Clonal fetal mesenchymal stem cells (cfMSCs) are isolated and clonally characterized fetal tissue-derived MSCs with demonstrated low allogeneity and multi-directional differentiation potential, which may modulate lung stromal cells, alveolar epithelial cells and airway epithelial cells to repair the damaged lung tissues and facilitate the regeneration of alveolar and airway structure, thus improving the lung ventilation as well as gas exchange function of the COPD patients. In addition, cfMSCs may secrete a variety of anti-inflammatory factors, growth factors and exosomes to inhibit the excessive inflammatory response in the lung tissue of COPD patients, improve the local microcirculation, and lay a foundation for the repair of damaged lung tissues.
This study aims to evaluate the safety, tolerability and preliminary efficacy of fully characterized cfMSCs in patients with moderate to severe COPD whose prior treatment has been ineffective. The research will provide a new clinical strategy for treating COPD and determine the optimal cell dosage, administration route and long-term therapeutic effect of the stem cell therapy, and open up a new path for the regenerative repair of lung damage caused by chronic respiratory diseases.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
cfMSCs to treat Chronic Obstructive Pulmonary Disease
Time frame: 24 weeks
Determine the safety and tolerability of clonal fetal Mesenchymal Stem Cell (cfMSC) therapy with Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, including acute reactions, fever and other adverse events.
Time frame: 48 weeks
Evaluate the changes of forced expiratory volume in one second (FEV1) to calculate the improvement rate of lung function compared with the baseline.
Time frame: 48 weeks
Evaluate the changes of carbon monoxide diffusion capacity (DLCO) to calculate the improvement rate of lung function compared with the baseline.
Time frame: 24 weeks
Determine blood inflammatory indicators including CRP, TNFa, IFNg, and IL-6 by molecular methods.
Time frame: 24 weeks
Analyze the blood cells related to inflammation index.
Time frame: 48 weeks
Evaluate the exercise capacity of patients by 6-minute walking distance test.
Time frame: 48 weeks
Assess the quality of life of patients by St. George's Respiratory Questionnaire (SGRQ) and COPD Assessment Test (CAT).
Time frame: 3 years
Count the number of acute exacerbations of COPD in patients after treatment, and compare the difference of acute exacerbation rate between the stem cell therapy group and the conventional treatment group.
Time frame: 3 years
Evaluate the progression-free survival and overall survival of patients.
Time frame: 3 years
Analyze the correlation between cfMSC therapy and long-term survival of COPD patients.
Contact information is provided by the study sponsor or research team.
Shenzhen Geno-Immune Medical Institute
Other
Clonal Fetal Mesenchymal Stem Cell Therapy for the Treatment of Chronic Obstructive Pulmonary Disease
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