Study of Pharmacokinetics, Pharmacodynamics, Safety of BCD-131 Compared to Mircera and Aranesp in Healthy Volunteers

Inclusion Criteria

• Signing of the Informed Consent Form;
• Male sex;
• Age of 18 to 45 years, inclusive;
• BMI within normal limits (18.5-24.9 kg/m2);
• Healthy patients, which is proved by their medical history, physical examination and laboratory findings:
• No clinically significant abnormalities of circulatory, respiratory, nervous, hematopoietic, endocrine and digestive systems, liver and kidneys in the past medical history and at screening;
• No history of cardiovascular disorders or thyroid disorders;
• No history of hematologic disorders, including but not limited to any type of anemia, myelodysplastic syndrome, blood cancers, hemolytic syndrome, hemoglobinopathies, coagulopathies;
• CBC results within normal limits, including:
• Hemoglobin within 132-173 g/L;
• Hematocrit (based on CBC results) within 39-49%;
• Platelet count within 150-400*109/L;
• Absolute reticulocyte count within 30.4-93.5 * 109/L;
• Blood biochemistry and urinalysis results within normal limits;
• Serum ferritin within 20-250 µg/L;
• Serum endogenous erythropoietin within 4.3-29.0 MIU/mL;
• Hemodynamic parameters within normal limits: systolic blood pressure within 100-139 mmHg; diastolic blood pressure within 60-90 mmHg; heart rate within 50-90 bpm;
• No history of chronic infections (tuberculosis) or chronic inflammation;
• No hepatitis B or C, HIV, or syphilis;
• No acute infections within 4 weeks prior to inclusion in the study;
• No psychiatric disorders and other conditions (including depression) that can interfere with the volunteer's ability to follow the study protocol;
• Well-being (in the volunteer's opinion) within 30 days prior to inclusion in the study;
• No history of or current (at baseline) alcohol or drug abuse;
• Ability of the volunteer, in the investigator's opinion, to follow the study protocol procedures;
• Willingness of volunteers and their sexual partners with preserved reproductive potential to use reliable contraception within 2 weeks before inclusion in the study and up to 7 weeks after the injection of the test product. This criterion is not applicable to subjects who underwent surgical sterilization. Reliable methods of contraception include one barrier method in combination with one of the following methods: spermicides, intrauterine device/oral contraceptives (for sexual partners).
• Willingness of volunteers to avoid alcohol intake within 24 hours before and 8 days after each injection of the test drug;

Exclusion Criteria

• History of treatment with erythropoietins or any other ESAs;
• Acute bleeding, blood/plasma donation or blood transfusion within 2 months before inclusion in the study;
• History of chronic bleeding;
• Standard laboratory and instrumental findings outside normal limits at screening;
• History of allergies (anaphylactic shock or multiple drug allergy syndrome);
• Known allergy or intolerance to any components of the investigational product;
• Major surgery within 30 days prior to screening, or surgery being scheduled for any time during the study;
• Impossibility to install a venous catheter for blood sampling (e.g. because of skin disorders at the sites of venipuncture);
• Diseases or other conditions that can interfere with the pharmacokinetics of the investigational drug (e.g. chronic liver, kidney, blood, circulatory system, lung or neuroendocrine diseases, including diabetes mellitus and others);
• History of fever of 40 °C or more;
• History of elevated hepatic transaminases (above 2.5xULN);
• Episodes of thrombosis and/or thromboembolia in past medical history (myocardial infarction, stroke, transient ischemic attacks, deep vein thrombosis, pulmonary embolism within 6 months prior to inclusion in the study) as well as an increased risk of deep vein thrombosis;
• History of epileptic attacks or seizures;
• History or current (at screening) depression, suicidal thoughts/ attempts;
• Regular oral or parenteral use of any medications including over-the-