Pilot Study of OMEGA-3 and Vitamin D in High-Dose in Type I Diabetic Patients

Prior treatment

• Uncompensated heart failure, fluid overload, myocardial infarction or liver disease or severe impairment of a vital organ within the last 6 weeks before enrollment.
• Current or ongoing use of non-insulin pharmaceuticals that affect glycemic control within prior 7 days of screening.
• Recent recipient of any licensed or investigational live attenuated vaccine(s) within 6 weeks of randomization.
• Use of investigational drugs within 3 months of participation.
• Concomitant therapy with immunosuppressive drugs, immunomodulators, or cytotoxic agents, or previous therapy less than 3 months from randomization.

Other illness

• Contra-indications to any of the drugs used in the trial (as per package insert, e.g., knowledge of hypersensitivity to drugs or its excipients).
• Ongoing acute infections, e.g., acute respiratory tract, urinary tract, or gastrointestinal tract infections.
• Ongoing or anticipated use of diabetes medications other than insulin.
• History or diagnosis of malignancy, with the exception of a history of localized basal or squamous cell carcinoma.
• History of gastroparesis or other severe gastrointestinal disease..
• History of mental illness deemed to be clinically unstable or any situation that, in the opinion of the investigator, would interfere with the participant's ability to comply with study requirements.
• History of illicit drug or alcohol abuse.

Lab values

• Any of the following laboratory findings indicating hemoglobin \<10.0 g/dL; leukocytes \<3,000/μL; neutrophils \<1,500/μL; lymphocytes \<800/μL; platelets \<100,000/μL.
• Any sign or diagnosis of significant chronic active infection (e.g., hepatitis, tuberculosis, EBV, or CMV), or screening laboratory evidence consistent with a significant chronic active infection (such as positive for HIV, IGRA test for TB, or hepatitis B-C).
• AST, ALT or Alkaline Phosphatase \>2 times upper limit of normal or total bilirubin \>1.5 times upper limit of normal.
• Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.

Age

• Pregnancy or ongoing breastfeeding for women; unwillingness or inability of both females and males of childbearing age to use a reliable and effective form of contraception, for the entire duration of the study.

Other

• Patients must not meet any of the following criteria to be eligible to participate:
• Inability or unwillingness of a participant to give written informed consent or comply with study protocol.
• BMI\>30 kg/m2.
• Presence of an allograft.

• Patients must meet all of the following criteria to be eligible to participate in this study:
• Subject must be able to understand and provide informed consent.
• Males and females, 6-17 years for children and 18-65 years of age for adult group.
• For new onset T1D - from onset to 6 months (180 days) post-diagnosis at the time of randomization.
• For established T1D - At least 6 months and up to 10 years from the diagnosis at the time of randomization.
• Affected by T1D, according to ADA standard criteria, and confirmed by positivity of at least one T1D-associated autoantibody, to GAD65, IA-2, ZnT8, or insulin autoantibody (if patient has been treated with insulin for less than 2 weeks).
• T1D must be treated with insulin (except if participant is in Honeymoon period/phase).
• Stimulated C-peptide peak level, at the baseline 1 visit MMTT, ≥ 0.2 ng/ml.
• Female subjects of childbearing potential must have a negative pregnancy test upon study entry.
• Adequate venous access to support study required blood draws.