A Study to Evaluate the Potential of Mesenchymal Stromal Cells to Treat Obliterative Bronchiolitis After Lung Transplantation (MSC in OB)
Primary Purpose
Bronchiolitis Obliterans, Lung Transplantation
Status
Completed
Phase
Phase 1
Locations
Australia
Study Type
Interventional
Intervention
MSC
Sponsored by
About this trial
This is an interventional treatment trial for Bronchiolitis Obliterans focused on measuring Mesenchymal stromal cells, Bronchiolitis obliterans, Lung transplant
Eligibility Criteria
Inclusion Criteria:
- Patients with single, bilateral or heart-lung allografts
- Patients with bronchiolitis obliterans syndrome (BOS) grades 2 & 3 (defined and graded according to international criteria (Appendix 1)), with evidence of deterioration in allograft function (i.e. deteriorating FEV1 or worsening BOS grade) within the last 12 months.
Patients with BOS grade 1 and evidence of deterioration in allograft function (i.e. deteriorating FEV1 or worsening BOS grade) within the last 12 months and at least one of the following additional risk factors for subsequent death:
- Single lung transplant
- Rapid deterioration (>20% fall in FEV1 in the previous 12 months)
- A pre-transplant diagnosis of usual interstitial pneumonia (pulmonary fibrosis) or pulmonary hypertension
Exclusion Criteria:
- Patients with active infection, acute allograft rejection, or airway anastomotic complications
- Patients with > 3 infective exacerbations of BOS in the last 12 months
- Patients with a history of cytomegalovirus (CMV) pneumonitis
- Patients with poor performance status and/or not expected to survive 3 months
- Patients who are pregnant or breastfeeding
- Patients with an allergy to beef products.
- Any condition that in the opinion of the Investigator may interfere with the safety of the patient, his / her completion of required follow-up visits or evaluation of the study objectives.
Sites / Locations
- TPCH
- RPH
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
MSC
Arm Description
Outcomes
Primary Outcome Measures
To establish the safety of infusions of MSC from related or unrelated HLA identical or HLA mismatched donors in the management of bronchiolitis obliterans syndrome after lung transplantation.
Secondary Outcome Measures
To document changes in lung function and 6 minute walk distance (6MWD) following infusion of MSC
To document survival post MSC infusion
Full Information
NCT ID
NCT01175655
First Posted
June 25, 2010
Last Updated
April 19, 2022
Sponsor
The Prince Charles Hospital
Collaborators
Cell and Tissue Therapies Western Australia
1. Study Identification
Unique Protocol Identification Number
NCT01175655
Brief Title
A Study to Evaluate the Potential of Mesenchymal Stromal Cells to Treat Obliterative Bronchiolitis After Lung Transplantation
Acronym
MSC in OB
Official Title
A Study to Evaluate the Potential of Mesenchymal Stromal Cells to Treat Obliterative Bronchiolitis After Lung Transplantation
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Prince Charles Hospital
Collaborators
Cell and Tissue Therapies Western Australia
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary aim of this study is to establish the safety of infusions of Mesenchymal Stromal Cells (MSC) from related or unrelated Human Leukocyte Antigen (HLA) identical or HLA mismatched donors in the management of bronchiolitis obliterans syndrome after lung transplantation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchiolitis Obliterans, Lung Transplantation
Keywords
Mesenchymal stromal cells, Bronchiolitis obliterans, Lung transplant
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MSC
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
MSC
Intervention Description
mesenchymal stromal cells (MSC), aiming for 2 x 106 /kg cells recipient body weight, aiming for a frequency of twice weekly for two weeks
Primary Outcome Measure Information:
Title
To establish the safety of infusions of MSC from related or unrelated HLA identical or HLA mismatched donors in the management of bronchiolitis obliterans syndrome after lung transplantation.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
To document changes in lung function and 6 minute walk distance (6MWD) following infusion of MSC
Time Frame
12 months
Title
To document survival post MSC infusion
Time Frame
12 months
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with single, bilateral or heart-lung allografts
Patients with bronchiolitis obliterans syndrome (BOS) grades 2 & 3 (defined and graded according to international criteria (Appendix 1)), with evidence of deterioration in allograft function (i.e. deteriorating FEV1 or worsening BOS grade) within the last 12 months.
Patients with BOS grade 1 and evidence of deterioration in allograft function (i.e. deteriorating FEV1 or worsening BOS grade) within the last 12 months and at least one of the following additional risk factors for subsequent death:
Single lung transplant
Rapid deterioration (>20% fall in FEV1 in the previous 12 months)
A pre-transplant diagnosis of usual interstitial pneumonia (pulmonary fibrosis) or pulmonary hypertension
Exclusion Criteria:
Patients with active infection, acute allograft rejection, or airway anastomotic complications
Patients with > 3 infective exacerbations of BOS in the last 12 months
Patients with a history of cytomegalovirus (CMV) pneumonitis
Patients with poor performance status and/or not expected to survive 3 months
Patients who are pregnant or breastfeeding
Patients with an allergy to beef products.
Any condition that in the opinion of the Investigator may interfere with the safety of the patient, his / her completion of required follow-up visits or evaluation of the study objectives.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Chambers, A/Prof
Organizational Affiliation
The Prince Charles Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
TPCH
City
Brisbane
State/Province
Queensland
ZIP/Postal Code
4032
Country
Australia
Facility Name
RPH
City
Perth
State/Province
Western Australia
ZIP/Postal Code
6000
Country
Australia
12. IPD Sharing Statement
Learn more about this trial
A Study to Evaluate the Potential of Mesenchymal Stromal Cells to Treat Obliterative Bronchiolitis After Lung Transplantation
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