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Clinical Trials/NCT02161744
NCT02161744
Terminated
Phase 1

A Phase I Open- Label Study to Assess the Safety, Tolerability, and Preliminary Efficacy of a Single Intravenous Dose of Autologous Adipose Stem Cell (Adult Human) to Subjects With Chronic Obstructive Pulmonary Disease

Arkansas Heart Hospital2 sites in 1 country9 target enrollmentOctober 10, 2013

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Arkansas Heart Hospital
Enrollment
9
Locations
2
Primary Endpoint
Safety of adipose derived stem cells (ADSC) in Patient with COPD
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is: 1.- to assess the safety and tolerability of autologous adipose derived stem cells (aADSC) administered intravenously in patients with chronic obstructive pulmonary disease, and 2.- to assess if this therapy results in less decrease of lung function parameters (FEV1, FEV1/FVC and 6 min walking distance) compared with a control baseline of 6 weeks.

Patients will be followed up for 12 months after the therapy.

Detailed Description

STUDY DESIGN This is a Phase I open- label single-dose study in subjects with significant COPD. This is an expanded safety cohort. The investigators will enroll a minimum of 30 subjects. 6 week data of FEV1, FEV1/FVC, DLCO and 6 min walking distance values will be collected in all patients who are enrolled in the study (Baseline and 6 weeks after). Prior to the stem cell treatment, the patient will be assessed for 6 weeks by pulmonary function tests and 6 min walk tests. Then, patients will receive the infusion of stromal vascular fraction cells containing the aADSC (single intravenous dose). The standard therapy of COPD patients will not be interrupted during the duration of the study. Safety will be monitored on an ongoing basis, and an interim safety review will be conducted by the Investigator(s) and Sponsor after the first 20 patients have been enrolled and treated.

Registry
clinicaltrials.gov
Start Date
October 10, 2013
End Date
October 29, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Arkansas Heart Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Males and Females ≥18 years.
  • Cognitive competitiveness.
  • Diagnosis of at least moderate COPD (postbronchodilator FEV1/FVC \< 70% (\<0.7), FEV1 \< 80% predicted).
  • Diffusing capacity impairment (DLCO) assessed by single breath test (corrected for alveolar volume, 'DLVA').
  • Life expectancy greater than 12 months.
  • Ability to understand and provide signed informed consent, or have a designated legal guardian or spouse legally able and willing to make such decisions on the subject's behalf.
  • Reasonable expectation that patient will receive standard post-treatment care and attend all scheduled safety follow-up visits.
  • No changes in active pulmonary medications for heart failure during the two weeks prior enrollment.
  • Written informed consent.
  • Non-smoker or Past smoker, with 20 pack-years or more history

Exclusion Criteria

  • Current smokers.
  • Unstable coronary disease.
  • Patients with industrial exposure to silica and/or asbestos or giant bullae.
  • Uncontrolled seizure disorder.
  • Presence of immune deficiency or autoimmune disease.
  • Alpha- 1 antitrypsin deficiency.
  • Cor pulmonale or diastolic heart failure NYHA class III or IV
  • Type 1 diabetes mellitus
  • Complicated type 2 diabetes mellitus.
  • Active tuberculosis or severe lung damage due to tuberculosis (extensive cavitation).

Outcomes

Primary Outcomes

Safety of adipose derived stem cells (ADSC) in Patient with COPD

Time Frame: 12 months

Safety/tolerability of Adipose Derived Stem Cell (ADSC) in patients with Chronic Obstructive Pulmonary Disease (COPD) during the twelve-month study period as determined by the incidence and severity of of adverse events.

Secondary Outcomes

  • Efficacy of ADSC In Pulmonary Function Test (PFTs)(2, 6, 12 months)
  • Efficacy of adipose derived stem cell in 6 MWT(2, 6, 12 months)
  • Efficacy in Quality of life using George's Respiratory Questionnaire(2, 6, 12 months)
  • Efficacy in Quality of life using the Chronic Respiratory questionnaires(2, 6, 12 months)
  • Efficacy of ADSC in improving Shortness of Breath (SOB)(2, 6 and 12 months)
  • Efficacy of adipose derived stem cells in patient's perceived exertion.(2, 6, 12 months)

Study Sites (2)

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