πŸ›οΈ Verified NIH Record β€’ Updated 2026-06-25

Type 1 Diabetes Extension Study (NCT02734277)

🟒 Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)

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

This is a multi-center, prospective, non-interventional study that focuses on the long- term effects following participation in selected ITN new-onset Type1 Diabetes Mellitus studies with immunomodulatory agents (T1DM, T1D). This observational study will: * follow participants to determine how long they continue to produce insulin, and * will also assess how changes in the immune system over time relate to the ability to produce insulin. This information could help design better therapies for type 1 diabetes in the future.

Who can join: Review the eligibility criteria below.

Location: UCSF School of Medicine β€” San Francisco, California

Age range: 8 Years to 35 Years

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (12 Sites)

  • UCSF School of Medicine β€” San Francisco, California
  • Stanford University β€” Stanford, California
  • University of Colorado School of Medicine: Barbara Davis Center for Diabetes β€” Aurora, Colorado
  • Yale University β€” New Haven, Connecticut
  • Emory University β€” Atlanta, Georgia
  • Indiana University Riley Hospital for Children β€” Indianapolis, Indiana
  • University of Iowa Health Care Division of Pediatric Endocrinology β€” Iowa City, Iowa
  • Joslin Diabetes Center β€” Boston, Massachusetts
  • University of Minnesota β€” Minneapolis, Minnesota
  • Children's Mercy Hospital β€” Kansas City, Missouri
  • Sanford Research β€” Sioux Falls, South Dakota
  • Benaroya Research Institute β€” Seattle, Washington

πŸ“ž Contact the Study Coordinator

Phone: (415) 476-5984

Email: rebecca.wesch@ucsf.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° 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 Β§ 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.

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—