Comparative Study of Rinsulin R (GEROPHARM) and Humulin Regular (Eli Lilly) Euglycemic Hyperinsulinemic Clamp Method

A double-blind, randomized, comparative, crossover study of the pharmacokinetics and pharmacodynamics of Rinsulin® R, solution for injection, 100 IU / ml (GEROPHARM LLC, Russia) and Humulin® Regular, solution for injection, 100 IU / ml (Lilly France, France) using euglycemic hyperinsulinemic clamp method on healthy volunteers

Inclusion criteria

• Signed informed consent to participate in the study.
• Men of the Caucasian race with a verified diagnosis "healthy" according to the data of standard clinical, laboratory and instrumental examination methods.
• Age 18-50, inclusive.
• Body mass index 18.5 - 27 kg / m2.
• Volunteers who have sexual contact with fertile women should agree to use barrier methods of contraception while participating in the study (unless they have undergone surgical sterilization). Study Participants must also not become a sperm donor within the specified period.
• Consent to all restrictions imposed during the study.

Exclusion criteria

• Acute inflammatory diseases within 3 weeks from the moment of complete recovery to the stage of screening.
• Presence of episodes of hypoglycemia in the history of the volunteer
• Presence in the family history of the closest relatives cases of verified diagnosis of diabetes mellitus of any type.
• Deviations from the norm of basic vital indicators (heart rate, blood pressure, respiratory rate, body temperature) and ECG from normal values and laboratory values from reference values during screening.
• Fasting plasma glucose> 6.1 mmol / L at screening.
• HbA1C> 6% at the time of screening.
• Oral glucose tolerance test - blood glucose level ≥7.8 mmol / L (2 hours after glucose loading) during screening.
• Hard-to-reach veins of the upper extremities, vein thrombosis, history of thrombophlebitis or family history of close relatives, "compromised" veins due to frequent preceding venipuncture.
• Taking medications, phytopreparations, biologically active additives within 14 days before screening.
• Significant blood loss 3 months before screening due to, for example, but not limited to the following points: a. donor blood donation; b. extended surgery or trauma leading to significant blood loss.
• Incomplete recovery from surgery or surgery scheduled while the volunteer is participating in the study.
• Mental, physical and other reasons interferes with adequately assessing behavior and correctly fulfill the conditions of the research protocol (incl. a history of mental illness).
• Presence or history (three years before the the study drug) of narcotic, drug and / or substance abuse.
• Positive test for the content of narcotic drugs in urine during the screening period.
• Anamnestic information about alcoholism or taking more than 10 units. alcohol per week (1 unit of alcohol is equivalent to 0.5 liters of beer, 200 ml of dry wine or 50 ml of spirits).
• Positive test for alcohol in breath during screening.
• Nicotine addiction (regular use of tobacco less than 6 months before screening).
• Any chronic diseases, incl. but not limited to positive test results for hepatitis C or hepatitis B, HIV, syphilis at the time of screening.
• Burdened allergological history.
• Presence of suspicion of an inflammatory disease of the urinary system based on the results of urinalysis during screening.
• Presence of oncological diseases within 5 years before the screening.
• History of organ transplantation (except of corneal transplant performed more than 3 months before the first injection of the study drug).
• Participation in a clinical trial of any drug or experimental medical device within 3 months prior to the first administration of the study drug.
• Any other condition that, in the reasonable opinion of the research physician, makes it difficult for the volunteer to participate in the study.

History of hypersensitivity to heparin, insulin or any of the excipients of the investigational drugs.