Exciting new study aiming to delay type 1 diabetes is launching in Australia soon

An exciting new study aiming to delay the progression of type 1 diabetes is launching soon in Australia

This heralds an important time to consider screening family members for the early markers of type 1 diabetes (islet autoantibodies)

Photo credit Breakthrough T1D
Two new trials investigating baricitinib to delay T1D – Breakthrough T1D

In a landmark move for type 1 diabetes (T1D) research, Eli Lilly and Company has announced the launch of two new global phase 3 clinical trials testing baricitinib, an oral medication aiming to delay or slow type 1 diabetes progression.

Baricitinib, is a medication known as a JAK inhibitor. It is already approved for autoimmune conditions like rheumatoid arthritis. The tablet targets overactive immune pathways while also protecting insulin-producing beta cells. The therapy gained attention after the Australian BANDIT trial—funded by Breakthrough T1D and led by Professor Tom Kay and our own Prof John Wentworth at St. Vincent’s Institute of Medical Research (SVI) in Melbourne—showed that baricitinib helped people recently diagnosed with T1D maintain their own insulin producing cells and spend more time in target glucose range.

Now, Lilly’s BARICADE program will build on that success with two key studies:

  • BARICADE-DELAY: testing whether baricitinib can prevent or delay the onset of T1D in people at high risk (stage 2).
  • BARICADE-PRESERVE: testing whether it can preserve beta cell function in people newly diagnosed with T1D (stage 3).

Both trials are double-blind, placebo-controlled, and will begin recruiting participants aged 1–36 years soon.

💬 “We’re thrilled that Lilly is advancing clinical research with baricitinib,” said Dr. Sanjoy Dutta, Chief Scientific Officer at Breakthrough T1D. “This brings us one step closer to making it available for people with type 1 diabetes.”

💬 Professor Kay added, “Baricitinib maintained insulin production for a year in our trial—a very exciting outcome. We hope the BARICADE studies confirm this and lead to real-world use for people with or at risk of type 1 diabetes.”

A smiling man in a suit with a light blue shirt and striped tie, set against a neutral gray background.
Prof Tom Kay, SVI, Melbourne

👉 Why it matters: Baricitinib represents a potentially game-changing, once-daily oral therapy that could preserve the body’s own insulin production—reducing the daily burden of T1D and improving long-term outcomes.

Community Engagement Panel – ATIC

Community Engagement Panel Members sought for ATIC

The Australasian Type 1 Diabetes Immunotherapy Collaborative (ATIC) brings together researchers, clinicians and advocates to identify and create immunotherapy clinical trial opportunities for people at every age and every stage of type 1 diabetes (T1D).

Supported by JDRF Australia, ATIC is led by St Vincent’s Institute of Medical Research (SVI) in Melbourne and involves multiple major type 1 diabetes centres across Australia and New Zealand.

Core to ATIC’s success is involvement of the broader type 1 diabetes community – people living with the condition, their families and advocates. People with first-hand experience of T1D are sought to join the ATIC Community Engagement Panel.

If you’re passionate about improving the lives of people with type 1 diabetes through immunotherapy research and ultimately treatments to delay and prevent T1D, don’t miss your chance to be a part of this exciting opportunity.

Applications are being accepted until COB Friday 2 December.

More information is available on the ATIC website:

https://atic.svi.edu.au/news-events/community-engagement-panel-calling-for-expressions-of-interest/

Trial for new T1D diagnosis

IMPACT Study for those newly diagnosed with T1D

Type1Screen is supporting the enrolment of young adults with a recent diagnosis of type 1 diabetes (T1D) to a new drug trial. This randomized, placebo-controlled, multi-centre clinical trial will evaluate the treatment of the Imotope™ IMCY-0098 and its effect on the preservation of beta-cell function in people with a recent onset T1D.

Aim

The study aims to investigate the effect of two doses of IMCY-0098 upon treatment-specific biomarkers and the effect of study medication on beta-cell function in adults with recently diagnosed type 1 diabetes.

Eligibility to take part

  • Aged 18 to 44 years
  • Diagnosed with type 1 diabetes (first insulin treatment) within 9 weeks of study screening visit.

How do I take part?

  • Contact Type1Screen via
    • email type1screen@mh.org.au
    • phone (03) 9342 7063