Diabetes Mellitus, Insulin-dependent Diabetes Mellitus
Conditions
Keywords
Juvenile diabetes, Diabetes, Insulin, Vaccine, Type 1 Diabetes, Diabetes Mellitus
Brief summary
Insulin dependent diabetes mellitus (also called type 1 diabetes mellitus or T1DM) is caused by the destruction of insulin-producing cells in the pancreas. People with T1DM do not produce enough insulin, which is necessary for proper regulation of blood sugar levels. T1DM is an autoimmune disease. An autoimmune disease is a disease in which the body's immune system attacks the body itself. In addition to regulating blood sugar, insulin may have the ability to protect cells in the pancreas from attack by the immune system. This study will evaluate whether an insulin-based vaccine can protect cells from autoimmune destruction. Study hypothesis: IFA-enhanced human insulin B-chain vaccination will lead to the arrest or slowing of the ongoing autoimmunity, and this will result in an appreciable difference in functioning B cell mass compared to the placebo treated group by the end of the study.
Detailed description
The vaccine in this study, IBC-VSO1, is a synthetic, metabolically inactive form of insulin designed to prevent pancreatic beta-cell destruction. It does not cause fluctuations in blood sugar. This study will evaluate whether the vaccine protects against autoimmune attack at the onset of T1DM, before pancreas function has deteriorated. This experimental treatment must occur early because 60% to 85% of beta-cells are already destroyed by the time of T1DM diagnosis. If beta-cell destruction can be halted, a prolonged remission period after diagnosis may occur, with a subsequent delay in diabetes-related complications. Participants must have been diagnosed with T1DM for no more than 3 months at the time of enrollment in this study. Participants will be randomly assigned to either a vaccine group or a control group. Participants in the vaccine group will receive one injection of IBC-VS01; participants in the control group will receive a placebo. Participants will then be monitored for 2 years. Participants will have ten follow-up visits, which will include blood tests for immunological and genetic analysis. Throughout the study, metabolic tests will also be performed to measure the remaining capacity of self insulin production of the body.
Interventions
BIOLOGICALIBC-VS01
IBC-VS01
BIOLOGICALIBC-VS01 placebo
IBC-VS01 placebo
Sponsors
Immune Tolerance Network (ITN)
National Institute of Allergy and Infectious Diseases (NIAID)
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No
Inclusion criteria
* Diagnosed with type 1 diabetes mellitus within 3 months prior to study entry * Positive for IAA, GAD65, or IA2 antibodies OR positive for GAD65 or IA2 antibodies after 2 weeks of starting insulin treatment
Exclusion criteria
* History of treatment with any oral hypoglycemic agent for more than 3 months * Ongoing use of medications known to influence glucose tolerance * History of immunosuppressive or steroid therapy for more than 3 months within the 2 years prior to study entry * Severe active liver, heart, kidney, or immunodeficiency disease that may limit life expectancy or may require immunosuppression during the study * Prior complications related to routine vaccinations * Prior participation in a trial for prevention of type 1 diabetes mellitus. Individuals who are known to have been in the placebo arm of a completed prevention trial are not excluded. * Any condition that may interfere with a participant's ability to comply with the study * Pregnancy or planned pregnancy within the time frame of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical endpoints including adverse events, local reactions, routine physical exams, insulin dose, and laboratory tests | Throughout study |
Secondary
| Measure | Time frame |
|---|---|
| C-peptide levels in response to mixed meal tolerance test | Throughout study |
| HbA1c, GAD65Ab, IAA, IA2Ab, GAD65Ab isotypes | Throughout study |
| CD4- and CD8- Va24JaQ+ | Throughout study |
| T cells' secretion of IL-4 and Interferon (IFN)-gamma | Throughout study |
Countries
United States
Outcome results
None listed