Safety, Tolerability, Immunological and Clinical Efficacy of Multiple Subcutaneous Doses of DiaPep277 in Latent Autoimmune Diabetes in Adults (LADA)

Exclusion Criteria

• •The subject has any significant diseases or conditions, including psychiatric disorders and substance abuse that, in the opinion of the site investigator, are likely to affect the subject's response to treatment or their ability to complete the study.
• •The subject has a history of any kind of malignant tumor.
• •The subject has secondary diabetes mellitus.
• •Within 2 weeks or 14 days of the Baseline Visit or during randomized treatment, the subject takes an oral anti-diabetic medication other than metformin to treat his/her diabetes.
• •The subject has clinical evidence of any diabetes-related complication that in the opinion of the site investigator would interfere with the subject's participation in and/or completion of the study.
• •The subject has a history of allergy or asthma that in the opinion of the site investigator would interfere with the subject's participation in and completion of the study.
• •The subject has a known immune deficiency from any disease, or a condition associated with an immune deficiency.
• •The subject is receiving immunosuppressive or immunomodulating agents or cytotoxic therapy, or any medication that, in the opinion of the site investigator, might interfere with the study.
• •The subject is a pregnant woman or a woman who is planning to become pregnant.
• •The subject has any of the following:
• •* chronic hepatitis or liver cirrhosis, or any other chronic liver disease
• •* is known to test positive for hepatitis B antigens or hepatitis C antibodies
• •* has abnormal liver function, defined as serum AST or ALT 3 times or more the upper limit of normal
• •The subject is a known or suspected drug abuser.
• •The subject has influenza-like symptoms on the day of dosing.
• •The subject is known to test positive for HIV antibodies.
• •The subject has chronic hematologic disease.
• •The subject has impaired renal function (serum creatinine greater than 1.4 mg/dL).
• •The subject has severe ketonuria (+++ on urine stix testing; ++ on repeated urine stix testing).
• •The subject has a BMI greater than 40kg/m2.
• •The subject has hyperlipidemia (fasting serum triglycerides \>1000 mg/dL). Suitable medical therapy for treatment of hyperlipidemia is allowed.
• •The subject has received any investigational drug within 3 months prior to Visit 1.
• •The subject has had a severe blood loss (400 mL or more, e.g., blood donation) within 2 months before the first dosing of the study medication.
• •The subject is a breast-feeding mother or planning to breast-feed.