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The type 1 research year in review: what genuinely moved in 2025

On 19 December 2025 Breakthrough T1D UK summed up a landmark year: teplizumab licensed, islet-cell results, UK screening data and smart-insulin progress.

Written by Updated 19 December 2025 3 min read
A researcher in a lab coat at work.
Photo by Julia Koblitz on Unsplash
The 60-second answer

The honest one-line version of 2025 is real progress on one front and hopeful groundwork on several others, with no cure. A UK charity, Breakthrough T1D, gathered the year’s Type 1 research highlights. The standout is teplizumab, the first drug that can delay Type 1 rather than only manage it, which reached approval.

  • The one that crossed the line was teplizumab, called the first disease-modifying therapy, meaning it changes the disease itself rather than only replacing insulin.
  • Cell therapies (lab-grown or engineered insulin-making cells) reported encouraging early results, but stayed at the small, first-in-human stage.
  • UK screening research looked at spotting Type 1 before symptoms, which is what makes a delay drug useful in the first place.
  • Smart insulin, an insulin meant to switch on and off with your glucose, moved forward in the lab but is not something you can be prescribed.
What actually changed

The one that crossed the line

Most research news is a step, not an arrival. In 2025, one thing genuinely crossed from lab to licence: teplizumab, approved as the first treatment that can delay Type 1 developing rather than simply managing it once it is here. For people found early, usually the relatives of someone who already has Type 1, that can mean extra time before insulin. It is worth being precise about why this counts as a landmark. For a hundred years, Type 1 care has meant replacing the insulin the body no longer makes. A drug that changes the timeline of the disease itself is a different kind of thing, even though it is only a delay, and only for people caught early.

Exciting but early

The news that is not ready yet

The rest of the year’s highlights are real, but they are research, not treatments. Engineered insulin-making cells that survive without harsh anti-rejection drugs made headlines, and deservedly so, but at the scale of a few patients watched over months. Screening studies explored how to catch Type 1 before it shows up, which pairs naturally with a delay drug. Smart insulin, which would ease off as your glucose drops and step up as it rises, kept progressing in the lab. None of these is something a UK clinic can offer you now. Filing them under hopeful groundwork, rather than imminent cure, is simply the accurate place to keep them.

What to notice

Reading research news without the whiplash

Ask what stage a story is at: lab, animal study, small trial, large trial, or approved. Usually only the last one changes care.
A UK-focused source like Breakthrough T1D or Diabetes UK is normally calmer and clearer than a viral headline.
Nothing from this year asks you to change how you manage your own Type 1 today.
What to ask your team

Questions that make an appointment useful

"Is there anything from this year of research that is actually relevant to my care now?"
"If I have relatives, is early screening for Type 1 something they could look into?"
"Are there UK research studies or registries I could join if I want to be involved?"
Sources