Diabetes Mellitus, Type 1 Clinical Trial
Official title:
Effect of Intravenous Alpha-1 Antitrypsin on Preserving Beta-cell Function in New-onset Type 1 Diabetes Mellitus (ITN041AI)- Part II
Aralast NP (alpha-1 antitrypsin, AAT), an alpha-1 proteinase inhibitor (human), was the drug
to be tested in this clinical trial. Aralast NP is an anti-inflammatory drug that affects
the cells that are thought to be involved in the development of type 1 diabetes mellitus
(T1DM, T1D). This study, known as RETAIN, was planned as a two-part trial to investigate the
effect of Aralast NP on preserving beta cell function and to determine if the intervention
would slow the progression of type 1 diabetes.
Part I of this trial (NCT 01183468) was an open-label, safety and dose level study
consisting of two groups. After completion of Part I, including a satisfactory safety
review, enrollment in Part II was to begin. Part II was designed as a two-arm, double-blind,
placebo-controlled clinical trial, and participants were to be randomly assigned to either
the Aralast NP treatment or placebo group.
T1D is an autoimmune disease. This means that your immune system (the part of your body that
helps fight infections) mistakenly attacks the cells that produce insulin (beta cells in the
pancreas). As beta cells are destroyed by your immune cells, your ability to produce insulin
is decreased. Insulin helps keep blood glucose levels normal.
Individuals with T1D who have the ability to produce some of their own insulin (even though
they still need to take insulin) may be able to achieve better glucose control than people
who produce no insulin at all. Better glucose control has been shown to reduce the long-term
complications of diabetes. Previous research has shown that giving medicines to affect the
immune system soon after type 1 diabetes is diagnosed may stop, delay or decrease the
destruction of beta cells, resulting in better glucose control.
In mouse models of disease, alpha-1 proteinase inhibitors have been shown to reverse
new-onset diabetes and induce a state of self-tolerance. The RETAIN clinical trial was
intended to investigate the effect of Aralast NP on preserving beta cell function and
slowing the progression of T1D.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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