A Study to Demonstrate Pharmacokinetic and Pharmacodynamic Biosimilarity Between HEC-Glargine and US-Lantus® in Healthy Male Volunteers

This is an interventional treatment trial for Type 1 Diabetes Mellitus focused on measuring pharmacokinetic, pharmacodynamic, euglycemic clamp technique, insulin glargine, biosimilarity study Read More

Inclusion Criteria:

• Participant has body weight not less than 60 kg and body mass index between 18.5 and 30.0 kg/m^2 (both inclusive).
• Glycohemoglobin (HbA1c) levels are <6.0%.
• Normal oral glucose tolerance test conducted within the previous 6 months
• Medical history, vital signs, physical examination, standard 12-lead electrocardiogram (ECG) and laboratory investigations should be clinically acceptable or within laboratory reference ranges for the relevant laboratory tests
• Non-smokers or mild to moderate smokers (≤ 10 cigarettes or pipes per day).

Exclusion Criteria:

• Evidence of psychiatric disorder, antagonistic personality, poor motivation, emotional or intellectual problems likely to limit the validity of consent to participate in the study or limit the ability to comply with protocol requirements.
• Current alcohol use >21 units of alcohol per week
• Regular exposure to substances of abuse (other than alcohol) within the past year.
• Use of any medication, prescribed or over-the-counter or herbal remedies
• Participation in another study with an experimental drug, where the last administration of the previous study drug was within 12 weeks before administration of study drug in this study.
• Treatment within the previous 3 months before the first administration of study drug with any drug with a well-defined potential for adversely affecting a major organ or system.
• A major disease (i.e., a disease that could not be treated at home, but the subject had to be hospitalized or needed general anesthesia usually for a major operation) during the 3 months before commencement of the screening period.
• Positive test for insulin antibodies.
• History of bronchial asthma or any other bronchospastic disease, and/or convulsions, and/or porphyria.
• Relevant history or laboratory or clinical findings indicative of acute or chronic disease, likely to influence study outcome.
• Resting pulse of >100 beats per minute (bpm) or <40 bpm during the screening period, either supine or standing.
• Hypertension diagnosed during screening or current diagnosis of hypertension.
• Hemoglobin count deviating more than 10% of the lower limit of normal.
• Clinically relevant abnormalities in the coagulation status.
• History of bleeding disorders.
• Veins unsuitable for venous blood collection and cannulation.
• Any specific study drug safety concern.