🏛️ Verified NIH Record • Updated 2026-08-20

A Study of Baricitinib (LY3009104) to Preserve Beta Cell Function in Children and Adults Newly Diagnosed With Type 1 Diabetes (BARICADE-PRESERVE) (NCT07222332)

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

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Eli Lilly and Company

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Barbara Davis Center for Childhood Diabetes — Aurora, Colorado

Age range: 1 Year to 35 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (138 Sites)

Showing the first 25 of 138 sites.

  • Barbara Davis Center for Childhood Diabetes — Aurora, Colorado
  • Tallahassee Memorial HealthCare — Tallahassee, Florida
  • Children's Hospital of Philadelphia (CHOP) — Philadelphia, Pennsylvania
  • Driscoll Children's Hospital — Corpus Christi, Texas
  • University of Virginia — Charlottesville, Virginia
  • Women's and Children's Hospital — Adelaide,
  • Centre for Children's Health Research — Brisbane,
  • Austin Health - Repatriation Hospital — Heidelberg West,
  • Ipswich Hospital — Ipswich,
  • Royal Children's Hospital — Melbourne,
  • Southern Adelaide Diabetes & Endocrine Services — Oaklands Park,
  • The Royal Melbourne Hospital — Parkville,
  • Perth Children's Hospital — Perth,
  • Sydney Children's Hospital — Randwick,
  • The Children's Hospital at Westmead — Westmead,
  • Université Libre de Bruxelles - Hôpital Erasme — Brussels,
  • UZ Brussel — Brussels,
  • Cliniques universitaires Saint-Luc — Brussels,
  • Antwerp University Hospital — Edegem,
  • UZ Gent — Ghent,
  • UZ Leuven — Leuven,
  • Centre Hospitalier Universitaire de Liège - Domaine Universitaire du Sart Tilman — Liège,
  • CHU UCL Namur/Site Sainte Elisabeth — Namur,
  • Université Catholique de Louvain-Namur - Centre Hospitalier Universitaire Dinant-Godinne - Site Godinne — Yvoir,
  • Hospital Universitário Maria Aparecida Pedrossian — Campo Grande,

📞 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.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗