Loading…
Effect of heat shock protein peptide DiaPep277 on ß-cell function in paediatric and adult patients with recent-onset diabetes mellitus type 1: two prospective, randomized, double-blind phase II trials
Background Aim of this trial was to test whether heat shock protein peptide DiaPep277 treatment in adult and paediatric patients with recent‐onset type 1 diabetes (T1D) is safe and whether it can preserve endogenous insulin production. Methods Two studies were performed in a prospective, multicentre...
Saved in:
Published in: | Diabetes/metabolism research and reviews 2007-05, Vol.23 (4), p.276-285 |
---|---|
Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Background
Aim of this trial was to test whether heat shock protein peptide DiaPep277 treatment in adult and paediatric patients with recent‐onset type 1 diabetes (T1D) is safe and whether it can preserve endogenous insulin production.
Methods
Two studies were performed in a prospective, multicentre, double‐blind, placebo‐controlled trial. Fifty adult (study p520, aged 16–44 years) and 49 paediatric patients (study p521, 4–15 years) with recent‐onset T1D were treated subcutaneously at four different time points with 0.2 mg or 1.0 mg DiaPep277 versus placebo and followed for 18 months. Adult patients were treated with 0.2 mg, 1.0 mg or 2.5 mg DiaPep277 versus placebo. Stimulated C‐peptide served as readout for functional ß‐cell‐mass.
Results
DiaPep277‐treatment was not associated with severe side effects. No differences were found in placebo and DiaPep277 treated groups. In adults, a modest trend towards better maintenance of ß‐cell function was observed in the 0.2 mg and 1.0 mg group, while there was significant loss of stimulated C‐peptide in the placebo and 2.5 mg group. Paediatric patients with low HLA risk showed stable C‐peptide levels until 13 months upon treatment with 1 mg DiaPep277. Despite similar stimulated C‐peptide levels at baseline, children exhibited a more pronounced loss of ß‐cell function over 18 months than adults (p = 0.0003).
Conclusion
Administration of DiaPep277 seems safe and may have beneficial effects on C‐peptide levels over time in some patients with T1D, but this finding was not accompanied by reduced HbA1c or insulin requirement. Studies with more patients and longer follow‐up are needed to further study the effect of DiaPep277. Copyright © 2007 John Wiley & Sons, Ltd. |
---|---|
ISSN: | 1520-7552 1520-7560 |
DOI: | 10.1002/dmrr.707 |