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Clinical Trials/NCT02057211
NCT02057211
Terminated
Phase 2

Mesenchymal Stem Cells to Intervene in the Development of Type 1 Diabetes: a Blinded Randomized Study

Uppsala University Hospital1 site in 1 country10 target enrollmentApril 2014

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Type 1 Diabetes Mellitus
Sponsor
Uppsala University Hospital
Enrollment
10
Locations
1
Primary Endpoint
∆-change of C-peptide Area Under the Curve (AUC) (0-120 min) for a mixed meal tolerance test at two year follow-up when compared to pre-treatment values at enrolment.
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

This project aims to evaluate the efficacy of autologous mesenchymal stem cell treatment to preserve insulin production and beta-cell mass in recently diagnosed patients with type 1 diabetes mellitus. The hypothesis to be tested is that an increased number of circulating mesenchymal stem cells will provide immune modulatory properties, and thereby stop the immune process in islets causing progressive beta-cell death.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
November 2017
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Per-Ola Carlsson

Professor

Uppsala University Hospital

Eligibility Criteria

Inclusion Criteria

  • fasting C-peptide \>0.12 nmol/l
  • within three weeks of diagnosis of type 1 diabetes

Exclusion Criteria

  • body mass index (BMI) \>30
  • unstable cardiovascular status incl. New York Heart Association (NYHA) class III/IV
  • patients with known or previous malignancy
  • active infections incl. serological evidence of infection with HIV, Treponema pallidum, hepatitis B (patients with serology consistent with previous vaccination and a history of vaccination are acceptable) or hepatitis C.
  • immune suppressive treatment
  • women being pregnant or nursing, or women physiologically capable of becoming pregnant, unless they are using effective methods of contraception during study

Outcomes

Primary Outcomes

∆-change of C-peptide Area Under the Curve (AUC) (0-120 min) for a mixed meal tolerance test at two year follow-up when compared to pre-treatment values at enrolment.

Time Frame: ∆-change will be assessed as a difference between two years after transplantation/sham transplantation of mesenchymal stem cells when compared to before transplantation/sham transplantation, i.e. at time 0.

Study Sites (1)

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