A Study of Baricitinib (LY3009104) for the Delay of Stage 3 Type 1 Diabetes in At-Risk Children and Adults (NCT07222137)
A Phase 3, Double-Blind, Randomized, Placebo-Controlled Study of Baricitinib to Delay Stage 3 Type 1 Diabetes in At-risk Participants Aged ≥1 to <36 Years
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this study is to find out if baricitinib can delay the onset of clinical type 1 diabetes (T1D) in people who are at high risk to develop T1D. Participation in the study will last up to approximately 5 years.
Who can join: Review the eligibility criteria below.
Location: Sansum Diabetes Research Institute — Santa Barbara, California
Age range: 1 Year to 35 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (113 Sites)
Showing the first 25 of 113 sites.
- Sansum Diabetes Research Institute — Santa Barbara, California
- Tallahassee Memorial HealthCare — Tallahassee, Florida
- University of South Florida — Tampa, Florida
- University of Iowa — Iowa City, Iowa
- Iowa Diabetes and Endocrinology Research Center — West Des Moines, Iowa
- Novak Center for Children's Health — Louisville, Kentucky
- Children's Hospital of Philadelphia (CHOP) — Philadelphia, Pennsylvania
- University of Virginia — Charlottesville, Virginia
- Women's and Children's Hospital — Adelaide,
- Box Hill Hospital — Box Hill,
- Royal Brisbane and Women's Hospital — Brisbane,
- Centre for Children's Health Research — Brisbane,
- Royal Children's Hospital — Melbourne,
- The Royal Melbourne Hospital — Parkville,
- Perth Children's Hospital — Perth,
- Sydney Children's Hospital — Randwick,
- The Children's Hospital at Westmead — Westmead,
- UZ Brussel — Brussels,
- Cliniques universitaires Saint-Luc — Brussels,
- Antwerp University Hospital — Edegem,
- UZ Leuven — Leuven,
- CHU UCL Namur/Site Sainte Elisabeth — Namur,
- Freire Pesquisa Clínica — Belo Horizonte,
- Centro de Diabetes Curitiba — Curitiba,
- Hospital Universitario Walter Cantidio — Fortaleza,
📞 Contact the Study Coordinator
Phone: (317) 615-4559
Email: LillyTrials@Lilly.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.