Airway Basal Stem Cell Therapy in Chronic Obstructive Pulmonary Disease (COPD)

Last updated: April 19, 2025
Sponsor: Ruijin Hospital
Overall Status: Active - Not Recruiting

Phase

1/2

Condition

Lung Disease

Emphysema

Bronchiectasis

Treatment

P63+ lung progenitors

Clinical Study ID

NCT06946953
20250322
  • Ages 40-80
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Diagnosed with COPD according to the 2021 Global Initiative for Chronic ObstructiveLung Disease (GOLD);

  2. Post-bronchodilator FEV1/FVC <70%;

  3. DLCO ≥20% and <80% of predicted value.

Exclusion

Exclusion Criteria:

  1. Pregnant, breastfeeding, or planning to become pregnant within 1 year aftertreatment (or male participants planning for their spouse to become pregnant);

  2. Positive for syphilis (TP-Ab), HIV, hepatitis B surface antigen (HBsAg), orhepatitis C virus (HCV) antibodies;

  3. Current or past history of malignancy.

Study Design

Total Participants: 20
Treatment Group(s): 1
Primary Treatment: P63+ lung progenitors
Phase: 1/2
Study Start date:
May 01, 2025
Estimated Completion Date:
December 31, 2029

Connect with a study center

  • Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

    Shanghai, Shanghai 200025
    China

    Site Not Available

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