About this trial
This study tests a three-phase immune treatment for people recently diagnosed with Type 1 diabetes (within 6 months, with some insulin production remaining).
Phase 1 (weeks 1-2): Teplizumab, an anti-CD3 antibody, is given by infusion to slow immune attack on insulin-producing beta cells.
Phase 2 (months 2-9): Insulin is injected directly into a lymph node (intralymphatic immunotherapy, ILIT) alongside low-dose interleukin-2 to teach the immune system to tolerate insulin and expand protective regulatory T cells.
Phase 3 (months 10-24): Low-dose interleukin-2 is continued to maintain immune tolerance.
The main goal is to preserve the body's remaining insulin production (measured by C-peptide). Sixty adults aged 18-45 will be randomly assigned to the MATIN-2 protocol or standard care. Safety, immune markers, and HbA1c will also be monitored.
Eligibility criteria
Qualifiers
Age 18-45 years
Clinical diagnosis of Type 1 diabetes mellitus within 6 months of enrolment
Positive for at least one diabetes-related autoantibody (GAD65, IA-2, ZnT8, or IAA)
Detectable fasting or stimulated C-peptide ≥ 0.2 nmol/L
Disqualifiers
Prior immunosuppressive therapy within 3 months
Active or chronic infection (HIV, hepatitis B/C, tuberculosis)
Current or prior malignancy within 5 years (except non-melanoma skin cancer)
Pregnancy or breastfeeding
Trial design
Treatments tested in this trial
- Teplizumab
- Intralymphatic Insulin Immunotherapy (ILIT)
Treatment groups
Locations
1Sponsors and collaborators
Abdullah Kars
Lead sponsor
Kara Harp Okulu (Turkish Military Academy)
Sponsor institution