Sequential Immune Modulation and Antigen-Specific Tolerance Induction for Disease Modification in Recent-Onset Type 1 Diabetes

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-45
SponsorAbdullah Kars

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

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Abdullah Kars

Lead sponsor

Kara Harp Okulu (Turkish Military Academy)

Sponsor institution