MSC Administration for the Management of Type 1 Diabetic Patients (DMT1-MSC)
Primary Purpose
Type 1 Diabetes Mellitus
Status
Unknown status
Phase
Phase 2
Locations
Chile
Study Type
Interventional
Intervention
MSCs
Sponsored by
About this trial
This is an interventional treatment trial for Type 1 Diabetes Mellitus focused on measuring Type1 Diabetes Mellitus, Multipotent stromal cell, Mesenchymal stem cell, Insulin, Pancreatic reserve, Disease progression
Eligibility Criteria
Inclusion Criteria:
- differential diagnosis of Type 1 Diabetes
- diagnosed performed at most 1 year before enrollment
- pancreatic reserve of insulin higher than 0.8 nmol/L/h
- good general health status
- informed consent of patient
- consent of treating physician
- proved psychiatric competence to be enrolled in a clinical study
Exclusion Criteria:
- pregnancy
- significant comorbidities
- HIV, HBV, HCV, HTLV-1, HLTV-2 or VDRL positive
Sites / Locations
- Clinica Alemana de Santiago
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
DMT1+MSCs
Arm Description
type 1 diabetic patients receiving a single dose of allogeneic ex vivo expanded mesenchymal stem cells
Outcomes
Primary Outcome Measures
Changes in insulin pancreatic reserve
Levels of insulin secreted after the acute ingestion of a protein rich liquid diet
Secondary Outcome Measures
Changes in insulin requirement
Daily dose of self-administered insulin
Full Information
NCT ID
NCT02893306
First Posted
August 27, 2016
Last Updated
September 1, 2016
Sponsor
Universidad del Desarrollo
Collaborators
Clinica Alemana de Santiago
1. Study Identification
Unique Protocol Identification Number
NCT02893306
Brief Title
MSC Administration for the Management of Type 1 Diabetic Patients
Acronym
DMT1-MSC
Official Title
Phase 2 Study of Intravenous Administration of Allogeneic Mesenchymal Stem Cells in Patients With Type 1 Diabetes Mellitus.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2012 (undefined)
Primary Completion Date
March 2017 (Anticipated)
Study Completion Date
March 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad del Desarrollo
Collaborators
Clinica Alemana de Santiago
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate whether the administration of multipotent stromal cell also referred as to mesenchymal stem cells (MSCs), modified Type 1 Diabetes progression.
Detailed Description
Aim: to evaluate whether a single intravenous administration of allogeneic bone marrow-derived multipotent stromal cell also referred as to mesenchymal stem cells (MSCs), modified endogenous insulin secretion capacity and exogenous insulin requirement in patients with Type 1 Diabetes Mellitus.
Participants: 10, females or males, 18 years or older, diagnosed with Type 1 Diabetes Mellitus at most 1 year before enrollment, under exogenous insulin treatment, with pancreatic reserve of insulin.
Intervention: intravenous administration of a single dose (2-3 millions/Kg) of allogeneic MSCs.
Follow up: before and 1, 6, 24 months after MSC administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus
Keywords
Type1 Diabetes Mellitus, Multipotent stromal cell, Mesenchymal stem cell, Insulin, Pancreatic reserve, Disease progression
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
DMT1+MSCs
Arm Type
Experimental
Arm Description
type 1 diabetic patients receiving a single dose of allogeneic ex vivo expanded mesenchymal stem cells
Intervention Type
Biological
Intervention Name(s)
MSCs
Other Intervention Name(s)
mesenchymal stem cells
Intervention Description
origin: bone marrow of healthy donor; manipulation: ex vivo expanded; via: intravenous; vehicle: 5% human recombinant albumin in physiological serum; dose: 2-3 millions/Kg; dosage: single
Primary Outcome Measure Information:
Title
Changes in insulin pancreatic reserve
Description
Levels of insulin secreted after the acute ingestion of a protein rich liquid diet
Time Frame
pre- and 1, 6, 24 months post-intervention
Secondary Outcome Measure Information:
Title
Changes in insulin requirement
Description
Daily dose of self-administered insulin
Time Frame
pre- and up to 24 months post-intervention
Other Pre-specified Outcome Measures:
Title
Number of patients with grade 3 through grade 5 adverse events (CTCAE v3.0)
Description
Review of patient clinical records
Time Frame
up to 24 months post-intervention
Title
Number of patients with grade 3 through grade 5 adverse events (CTCAE v3.0)
Description
Regular communication with patient and his/her physician in order to be informed of eventual complications
Time Frame
up to 24 months post-intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
differential diagnosis of Type 1 Diabetes
diagnosed performed at most 1 year before enrollment
pancreatic reserve of insulin higher than 0.8 nmol/L/h
good general health status
informed consent of patient
consent of treating physician
proved psychiatric competence to be enrolled in a clinical study
Exclusion Criteria:
pregnancy
significant comorbidities
HIV, HBV, HCV, HTLV-1, HLTV-2 or VDRL positive
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paulette Conget, PhD
Organizational Affiliation
Universidad del Desarrollo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claudio Mizon, MD
Organizational Affiliation
Clinica Alemana de Santiago
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinica Alemana de Santiago
City
Santiago
State/Province
Region Metropolitana
Country
Chile
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be publish in a peer review journal
Citations:
PubMed Identifier
22644660
Citation
Ezquer F, Ezquer M, Contador D, Ricca M, Simon V, Conget P. The antidiabetic effect of mesenchymal stem cells is unrelated to their transdifferentiation potential but to their capability to restore Th1/Th2 balance and to modify the pancreatic microenvironment. Stem Cells. 2012 Aug;30(8):1664-74. doi: 10.1002/stem.1132.
Results Reference
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PubMed Identifier
21304603
Citation
Ezquer F, Ezquer M, Simon V, Conget P. The antidiabetic effect of MSCs is not impaired by insulin prophylaxis and is not improved by a second dose of cells. PLoS One. 2011 Jan 27;6(1):e16566. doi: 10.1371/journal.pone.0016566.
Results Reference
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PubMed Identifier
18489988
Citation
Ezquer FE, Ezquer ME, Parrau DB, Carpio D, Yanez AJ, Conget PA. Systemic administration of multipotent mesenchymal stromal cells reverts hyperglycemia and prevents nephropathy in type 1 diabetic mice. Biol Blood Marrow Transplant. 2008 Jun;14(6):631-40. doi: 10.1016/j.bbmt.2008.01.006. Epub 2008 Apr 14.
Results Reference
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MSC Administration for the Management of Type 1 Diabetic Patients
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