The Intranasal Insulin Trial (INIT II) began in late 2006, and is being run by an Australian non-profit organization, the Diabetes Vaccine Development Centre (DVDC). The aim of the trial is to test a new preventative treatment for type 1 diabetes in young people who are at risk of developing this condition.
INIT II is a randomized, double-blind, placebo-controlled multi-centre clinical trial, which will determine whether intranasal insulin can delay or prevent the onset of type 1 diabetes in children and young adults at risk.
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Background
Pre-clinical Evidence
There is evidence from a mouse model of type 1 diabetes that the administration of intranasal insulin can reduce the immune attack on the insulin-producing beta cells of the pancreas, thus acting as a vaccine against the condition. In pre-clinical tests, insulin was administered onto the nasal mucosa of mice with a genetic predisposition to type 1 diabetes. This caused the induction of regulatory T-cells, which were protective against the destruction of beta cells in the mice.
INIT I
The predecessor of INIT II, the INIT I trial was designed to test safety. 38 individuals were treated with either intranasal insulin spray or placebo, daily for 10 days, and then 2 days a week for 6 months. The trial showed that intranasal insulin does not accelerate the onset of diabetes. An immune effect was also observed in children and young adults at risk of type 1 diabetes. Intranasal insulin produced effects that suggested a change in the immune attack on the insulin-producing beta cells.
Intranasal Insulin Video
Trial design
Based on the success of INIT I, the INIT II trial will test whether intranasal insulin can delay or prevent type 1 diabetes in a larger population.
Eligibility
A significant feature of the INIT II trial is the recruitment of people at risk for type 1 diabetes. The trial requires 120 participants, aged between 4 and 30. To enter the treatment arm of the trial, participants must have two or more antibodies (against insulin, GAD65, and tyrosine phosphatase-like insulinoma antigen 2), but a normal response in a glucose tolerance test. This indicates that they are at high risk of developing type 1 diabetes, but significant destruction of the pancreatic beta cells has not yet occurred.
To find enough eligible people, relatives of people with type 1 diabetes are screened for antibodies. Those who are positive undergo a glucose tolerance test to make sure they do not already have diabetes. Although type 1 diabetes can be hereditary, the probability that a family member of someone with type 1 diabetes will meet the criteria to enter the trial is only around 2-3%. It is therefore expected that over 12,000 people will need to be screened.
Treatment arm
After screening, participants are staged into a treatment arm. One group receives placebo solution, and the other receives a solution that contains 440IU of insulin. The treatment is self-administered using a nasal spray every morning for 7 consecutive days, and then once a week for 12 months. During this time, participants are monitored every three months, then every six months for a further four years.
The trial is taking place at a number of centers across Australia, New Zealand and Germany including,
- Mater Children's Hospital, Brisbane
- Women's and Children's Hospital, Adelaide
- Princess Margaret Hospital, Perth
- Royal Melbourne Hospital, Melbourne
- Monash Medical Centre, Melbourne
- The Children's Hospital at Westmead, Sydney
- Royal North Shore Hospital, Sydney
- Canberra Hospital, Canberra
- Liggins Institute, Auckland, New Zealand
- Forschergruppe Diabetes der TU M?nchen
Endpoint
The primary clinical endpoint of INIT II is the development of type 1 diabetes. This is expected to be lower in participants who were exposed to insulin.
Source of the article : Wikipedia
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