The goal of this clinical trial is to test whether the combination of two safe immune therapies called abatacept and nasal insulin can preserve pancreas function in recently-diagnosed type 1 diabetes. When type 1 diabetes is first diagnosed, the pancreas is still able to make small amounts of insulin, which helps control glucose levels. Preserving pancreas function can make glucose control easier and reduce the need to use injected insulin. Participants will be asked to inject abatacept under their skin once per week and inhale nasal insulin or nasal placebo using a spray for 10 consecutive days initially and twice per week thereafter. The treatment period is for 48 weeks, with another 48-week follow-up period.
Type 1 diabetes is caused by an immune attack on insulin-producing beta cells of the pancreas that impairs their ability to make insulin to control blood glucose levels. When diabetes is diagnosed, the pancreas is usually still able to make some insulin, but not enough to meet the body's needs. Over time, continued immune attack further decreases insulin production until after one to two years it is very low or undetectable. When type 1 diabetes is diagnosed, treatments that stop the immune attack may preserve residual beta-cell function. This decreases the requirement for injected insulin and improves glucose control. However, so far, immune therapies have not been shown to prevent ongoing loss of beta-cell function. In this clinical trial, two safe immune therapies called abatacept and nasal insulin will be used together to test if the combination can better preserve the function of beta cells to make insulin after diagnosis. If this occurs, it will be relatively simple to develop this treatment for routine use in recently-diagnosed people and to test whether it prevents high-risk individuals progressing to need insulin injections. This trial will also provide research samples to improve our understanding of how type 1 diabetes develops and how abatacept and nasal insulin might affect this process. The new knowledge created from studying these samples will improve our ability to use abatacept and nasal insulin to preserve pancreas function in type 1 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
68
Abatacept injected subcutaneously once per week and nasal insulin inhaled for 10 consecutive days initially and twice per week thereafter
Abatacept injected subcutaneously once per week and nasal placebo inhaled for 10 consecutive days initially and twice per week thereafter
The Children's Hospital at Westmead
Westmead, New South Wales, Australia
Queensland Children's Hospital
South Brisbane, Queensland, Australia
Women's and Children's Hospital
North Adelaide, South Australia, Australia
The Royal Melbourne Hospital
Parkville, Victoria, Australia
The Royal Children's Hospital
Parkville, Victoria, Australia
Perth Children's Hospital
Nedlands, Western Australia, Australia
Beta-cell function at 48 weeks
Change in average C-peptide concentration during a 2-hour mixed meal challenge
Time frame: 0 weeks - 48 weeks
Beta-cell function at 24, 72 and 96 weeks
Change in average C-peptide concentration during a 2-hour mixed meal challenge
Time frame: 0, 24, 72 and 96 weeks
Glucose regulation
Proportion of time in the range 3.9-10mmol/l, time below 3.9mmol/l and glucose %CV measured by continuous glucose monitoring (CGM)
Time frame: 0, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 60, 72 and 96 weeks
Estimated C-peptide concentration
Average C-peptide concentration estimated from fasting glucose, C-peptide, HbA1c, body mass index, disease duration and insulin dose
Time frame: -2, 24, 48, 72 and 96 weeks
Frequency of hypoglycemic events
Frequency of glucose readings \<3.0mmol/l, determined by CGM and correcting for CGM wear time
Time frame: 0, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 60, 72 and 96 weeks
Hemoglobin A1c levels
Change in HbA1c levels
Time frame: 0, 12, 24, 36, 48, 60, 72 and 96 weeks
Insulin use
Daily insulin dose at all visits
Time frame: Every 4 weeks for 96 weeks
Weight, body mass index and sitting blood pressure
Change in weight, body mass index and blood pressure
Time frame: 0, 12, 24, 48, 60, 72 and 96 weeks
Diabetes antibody levels
Insulin, GAD, IA2 and ZnT8 autoantibody concentrations
Time frame: -2, 0, 4, 12, 24, 48, 60, 72 and 96 weeks
Quality of life assessment
Assessed by questionnaire
Time frame: -2, 0, 24, 48, 72 and 96 weeks
Adverse events
Frequency and severity of adverse events
Time frame: All visits for 96 weeks
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