The study will be a non-randomized, open label, single dose, single blind, placebo control, single center, single arm study in Type I diabetes patients. The study will include single dose administration for the evaluation of single dose acute toxicity, pharmacokinetics and activity.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
8
Oral insulin single administration
Assaf Harofe Medical Center
Zrifin, Beer-Yaakov, Israel
Adverse events occurrence
Time frame: one month
Evaluate the glucose lowering effect of Oshadi Oral Insulin
Time frame: 12 hours following administration
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