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NCT Number: NCT07477600

cfMSC Stem Cell Therapy Targeting COPD

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.

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Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Shenzhen Geno-immune Medical Institute

Shenzhen, Guangdong, 518000, China

Location status: Recruiting

Location contact

Lung-Ji Chang, Ph.D

CONTACT

[email protected]

+86 0755-86573763

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ability to understand the study protocol and the willingness to provide written informed consent;
  • Age 40-80 years old, male or female;
  • Diagnosed with moderate to severe COPD according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines (GOLD Ⅱ-Ⅳ).
  • Regular use of COPD conventional drugs for more than 3 months, and the condition is stable for more than 4 weeks;
  • ineffective clinical treatment;
  • Life expectancy > 6 months;
  • At least six months smoking cessation, including non-smoking during the treatment and follow-up periods of the study.

Exclusion criteria

  • Combined with other serious lung diseases: asthma, active pulmonary tuberculosis, bronchiectasis, pulmonary embolism, interstitial lung disease, pulmonary hypertension, etc.;
  • A history of lung surgery (pneumonectomy, lung volume reduction surgery, etc.) or bronchial intervention surgery within 12 months;
  • Invasive or non-invasive mechanical ventilation history within 4 weeks, or moderate to severe acute exacerbation of COPD within 4 weeks;
  • Negative for HIV, HCV or syphilis serology;
  • A history of malignant tumors or malignant tumors under treatment;
  • Autoimmune diseases requiring long-term use of glucocorticoids or immunosuppressants;
  • Poorly controlled diabetes (fasting blood glucose > 10.0 mmol/L) or severe metabolic diseases;
  • A history of alcohol or drug abuse, or mental diseases that cannot cooperate with the study;
  • Pregnancy or breastfeeding.
  • Unable or unwilling to comply with study specific schedules or procedures.

Treatment and study plan

clonal fetal MSCs

Biological

cfMSCs to treat Chronic Obstructive Pulmonary Disease

Primary outcomes

  1. Number of patients with adverse events.

    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.

Secondary outcomes

  1. Lung function index changes

    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.

  2. Lung function index changes

    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.

  3. Inflammatory indicator changes

    Time frame: 24 weeks

    Determine blood inflammatory indicators including CRP, TNFa, IFNg, and IL-6 by molecular methods.

  4. Inflammatory indicator changes

    Time frame: 24 weeks

    Analyze the blood cells related to inflammation index.

  5. Exercise capacity and quality of life

    Time frame: 48 weeks

    Evaluate the exercise capacity of patients by 6-minute walking distance test.

  6. Quality of life

    Time frame: 48 weeks

    Assess the quality of life of patients by St. George's Respiratory Questionnaire (SGRQ) and COPD Assessment Test (CAT).

  7. Acute exacerbation rate of COPD

    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.

  8. Survival status of patients

    Time frame: 3 years

    Evaluate the progression-free survival and overall survival of patients.

  9. Survival status of patients

    Time frame: 3 years

    Analyze the correlation between cfMSC therapy and long-term survival of COPD patients.

Study contacts

Contact information is provided by the study sponsor or research team.

Lung-Ji Chang, Ph.D

CONTACT

[email protected]

+86 0755-86573763

Sponsors and collaborators

Lead sponsor

Shenzhen Geno-Immune Medical Institute

Other

Registry information

Official study title

Clonal Fetal Mesenchymal Stem Cell Therapy for the Treatment of Chronic Obstructive Pulmonary Disease

Important dates

Study start
2026
Primary completion
2029
Study completion
2030
First posted
Mar 17, 2026
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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