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NCT07477600Not yet recruitingPhase 1/2

cfMSC Stem Cell Therapy Targeting COPD

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

Source: ClinicalTrials.gov · Last updated 2 Nov 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
30 (estimated)
First submitted
10 Mar 2026
Start date
30 Jun 2027
Primary completion date
30 Jun 2029
Lead sponsor
Shenzhen Geno-Immune Medical Institute
Diseases
COPD
NCT number
NCT07477600

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 30
  • From 30 Jun 2027 to the primary completion date, 30 Jun 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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;
  • 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;
  • A history of alcohol or drug abuse, or mental diseases that cannot cooperate with the study;

Lab values

  • Poorly controlled diabetes (fasting blood glucose \> 10.0 mmol/L) or severe metabolic diseases;

Other

  • Invasive or non-invasive mechanical ventilation history within 4 weeks, or moderate to severe acute exacerbation of COPD within 4 weeks;
  • Pregnancy or breastfeeding.
  • Unable or unwilling to comply with study specific schedules or procedures.

Who the study is looking for

  • 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.

Age in the registry: 40 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Shenzhen Geno-immune Medical Institute
Coordinator of this site? Confirm its status
ShenzhenChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.