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Taking people in BelgiumPhase 3

Testing baricitinib to protect insulin-making cells in new type 1 diabetes

Tests baricitinib against placebo in people newly diagnosed with type 1 diabetes.

Plain-language title generated from the registry record
Registry title: A Study of Baricitinib (LY3009104) to Preserve Beta Cell Function in Children and Adults Newly Diagnosed With Type 1 Diabetes (BARICADE-PRESERVE)

Key facts

Where
Anderlecht, Edegem, Gent, Jette, Leuven, Liège, Namur, Sint-Lambrechts-Woluwe, and Yvoir, BelgiumSee the 9 sites
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 1 and 35 years old?

Source: NCT07222332, who can take part

Where in Belgium

  • Hopital ErasmeAnderlecht, BelgiumTaking people
  • Universitair Ziekenhuis AntwerpenEdegem, BelgiumTaking people
  • Universitair Ziekenhuis GentGent, BelgiumTaking people
  • UZ BrusselJette, BelgiumTaking people
  • UZ LeuvenLeuven, BelgiumTaking people
  • Centre Hospitalier Universitaire de LiègeLiège, BelgiumTaking people
  • Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-NamurNamur, BelgiumTaking people
  • Cliniques Universitaires Saint-LucSint-Lambrechts-Woluwe, BelgiumTaking people
  • Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-NamurYvoir, BelgiumTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Eli Lilly and Company
Trial code
NCT07222332EU 2025-522170-36-00
Record updated
4 November 2026
Original description
The purpose of this study is to find out if baricitinib can preserve beta-cell function in participants newly diagnosed with type 1 diabetes. Participation in the study will last about 60 weeks.Read full original descriptionShow less

A Phase 3, Double-Blind, Randomized, Placebo-Controlled Study of Baricitinib to Preserve Beta Cell Function in Participants Newly Diagnosed With Type 1 Diabetes Aged ≥1 to <36 Years

The purpose of this study is to find out if baricitinib can preserve beta-cell function in participants newly diagnosed with type 1 diabetes. Participation in the study will last about 60 weeks.

Inclusion: Have a new diagnosis of type 1 diabetes within 100 days prior to starting study intervention; Have at least one diabetes-related autoantibody found at screening; Show signs of remaining beta-cell function; stimulated (peak or 90 min) C-peptide ≥0.2 nmol/L (0.6 ng/mL) at screening; Weigh at least 8 kilograms (kg) (18 pounds) at screening.

Exclusion: Have any other type of diabetes including gestational; Have had a heart attack, heart disease, stroke, or heart failure; Have a history or high risk of venous thromboembolism, lymphoproliferative disease or malignancy; Have a current or recent clinically serious medical condition or infection; Have uncontrolled high blood pressure.

ClinicalTrials.gov NCT07222332 · EU CTIS 2025-522170-36-00