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NCT Number: NCT06946953

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

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.

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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

Ruijin Hospital Hainan Branch, Shanghai Jiao Tong University School of Medicine, Qionghai, Hainan, China

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

P63+ lung progenitors

Biological
  • Patient Screening and Cell Collection:

Eligible patients will undergo sample collection at the study center or authorized tertiary hospitals. The operator will collect samples via bronchial brushing from three healthy segments of the patient's 3-5 level bronchi. The samples will be transported to a cooperative production facility for isolation and preparation. The cell preparation cycle is approximately 4-8 weeks. Patients will bear the costs of this process.

  • Transplantation Therapy:

Transplantation therapy will be conducted at Ruijin Hainan Hospital. The cell preparation will be administered via fiberoptic bronchoscopy to each lung segment, with one dose per patient. After infusion, patients are advised to remain hospitalized for 24-48 hours for observation.

  • Post-Treatment Follow-Up:

Patients are advised to return for examination and evaluation at 4 and 24 weeks post-treatment.

Other names: Lung progenitors, Airway basal stem cells

Primary outcomes

  1. Change in DLCO from baseline.

    Time frame: 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.

Secondary outcomes

  1. Change in FEV1 from baseline.

    Time frame: Baseline, 4 weeks post treatment, 24 weeks post treatment

  2. Change in FVC from baseline.

    Time frame: Baseline, 4 weeks post treatment, 24 weeks post treatment

  3. Improvement in CAT score (symptoms, activity, and psychological status).

    Time frame: Baseline, 4 weeks post treatment, 24 weeks post treatment

    CAT, COPD Assessment Test. Score range: 0 to 40. Higher scores indicate a worse outcome.

Other outcomes

  1. Incidence of adverse events and serious adverse events.

    Time frame: Through study completion, an average of 6 months

    Safety Evaluation

Study contacts

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

Jiayang Yan

CONTACT

[email protected]

+8619821839207

Sponsors and collaborators

Lead sponsor

Ruijin Hospital

Other

Registry information

Important dates

Study start
2025
Primary completion
2029
Study completion
2029
First posted
Apr 27, 2025
Registry last updated
Jul 21, 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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