Skip to content

Autologous Bronchial Basal Cell Transplantation for Treatment of COPD

A Single-centered, Non-randomized, Concurrent Control Study on Autologous Bronchial Basal Cell Transplantation for Treatment of Chronic Obstructive Pulmonary Disease (COPD)

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03188627
Enrollment
24
Registered
2017-06-15
Start date
2018-06-12
Completion date
2019-12-26
Last updated
2023-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Brief summary

Chronic Obstructive Pulmonary Disease (COPD) is usually characterized by long-term poor airflow, resulting in chronic pulmonary heart disease, chronic respiratory failure or even death. For COPD patients, pulmonary bronchus structures are damaged and cannot be repaired by recent clinical methods so far. This study intends to carry out a single-centered and non-randomized phase I/II clinical trial with concurrent controls to investigate whether bronchial basal cells can regenerate damaged lung tissue. During the treatment, bronchial basal cells will be isolated from patients' own bronchi and expanded in vitro. After careful characterization, expanded cells will be transplanted autologously into the lesion by fiberoptic bronchoscopy. The safety and efficacy of the treatment will be monitored by measuring the key clinical indicators.

Interventions

Transplantation of autologous bronchial basal cells

Sponsors

Southwest Hospital, China
CollaboratorOTHER
Tongji University
CollaboratorOTHER
Regend Therapeutics
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 40 to 75; * Diagnosed with COPD according the guideline (a. with symptoms of productive cough, sputum production or shortness of breath; b. with poor airflow as indicated by FEV1\<70% predicted value and FEV1/FVC \< 0.7 in pulmonary function test; c. with exclusion of other pulmonary disease by CT or blood examination.); * Current smoker or ex-smoker with a history of no less than 10 years or 10 packs/year; * Tolerant to bronchofiberscope; * Written informed consent signed.

Exclusion criteria

* Pregnant or lactating women; * Patients positive for syphilis, HIV; * Patients with malignant tumor; * Patients with serious significant pulmonary infection and need anti-infection treatment; * Patients with serious heart disease(NYHA class Ⅲ-Ⅳ); * Patients with a history of abusing alcohol and illicit drug; * Patients participated in other clinical trials in the past 3 months; * Patients assessed as inappropriate to participate in this clinical trial by investigator.

Design outcomes

Primary

MeasureTime frameDescription
Indicators for safety1-6 monthsMeasured by blood routine test, urine routine test and blood chemistry panels
Diffusion capacity of CO (DLCO)1-6 monthsOne of the indicators in pulmonary function test, the extent to which oxygen passes from the air sacs of the lungs into the blood

Secondary

MeasureTime frameDescription
Maximum mid-expiratory flow (MMF)1-6 monthsOne of the indicators in pulmonary function test, standing for maximal (mid-)expiratory flow and is the peak of expiratory flow as taken from the flow-volume curve and measured in liters per second
Maximum voluntary ventilation (MVV)1-6 monthsOne of the indicators in pulmonary function test, measuring the maximum amount of air that can be inhaled and exhaled within one minute
Forced expiratory volume in one second (FEV1)1-6 monthsOne of the indicators in pulmonary function test, a marker to assess airway obstruction
St. George's respiratory questionnaire (SGRQ) scale1-6 monthsA questionnaire to assess life quality affected by the respiratory problems
Modified medical research council (MMRC) chronic dyspnea scale1-6 monthsAn indicator to evaluate the level of dyspnea
Imaging of lung by high resolution computed tomography (HR-CT)1-6 monthsHR-CT images of lung will be analyzed to indicate the pulmonary structure.
Forced vital capacity (FVC)1-6 monthsOne of the indicators in pulmonary function test, indicating the maximum amount of air a person can expel from the lungs after a maximum inhalation
6-minute-walk test (6MWT)1-6 monthsAn indicator to evaluate the exercise function of patients with moderate or severe pulmonary heart diseases
The ratio of forced expiratory volume in the first one second to the forced vital capacity (FEV1/FVC)1-6 monthsOne of the indicators in pulmonary function test, representing the proportion of a person's vital capacity that they are able to expire in the first second of forced expiration to the full vital capacity

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026