A Safety, Pharmacokinetics and Pharmacodynamics Study of GNR-086 and Ilaris® in Healthy Volunteers

Generium

Status and phase

Completed

Phase 1

Conditions

Healthy Volunteers

Treatments

Biological: GNR-086

Biological: Ilaris®

Study type

Interventional

Funder types

Industry

Identifiers

NCT06481189

CAN-HVL-I

Details and patient eligibility

About

This is a randomized single-blind comparative parallel group study of the safety, pharmacokinetics and pharmacodynamics of GNR-086 and Ilaris® in healthy volunteers. Participants received a single subcutaneous dose of canakinumab 150 mg. The follow up period was 120 days.

Full description

GNR-086 (canakinumab) is being developed as a biosimilar to the drug Ilaris®, a lyophilisate for the preparation of solution for subcutaneous administration.

Canakinumab is a recombinant human monoclonal antibody against human interleukine-1β that belongs to the immunoglobulin G1/k (IgG1/k) isotype subclass.

This study is intended for a comparative study of the safety, pharmacokinetics and pharmacodynamics of the drug GNR-086 and the reference drug Ilaris® for the purpose of registration of the drug - GNR-086 (JSC GENERIUM, Russia), 150 mg, lyophilisate for the preparation of solution for subcutaneous administration in the Russian Federation. The study included healthy volunteers aged 18-45 years at the time of signing the informed consent form. The study included a screening period, single administration of study/comparator drug and a follow up period. Allocation of patients to treatment groups was carried out by randomization in a ratio of 1:1 to the study drug and comparator drug. 105 patients (53 to the study drug group and 52 to the comparator drug group) were randomized.

Enrollment

105 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Written informed consent to participate in the study, obtained from the volunteer before the start of any procedures related to the study;
Men and women aged 18 to 45 years, inclusive, at the time of signing the informed consent form;
Verified diagnosis "healthy" (the diagnosis "healthy" is established on the basis of a detailed medical history, in the absence of deviations from normal values during a clinical examination, including measurement of blood pressure, heart rate, respiratory rate, body temperature, as well as laboratory data studies, results of electrocardiography and fluorography);
Body weight from 50 to 85 kg, body mass index from 18.5 to 28 kg/m2, inclusive.
Agreement to adhere to adequate methods of contraception during the entire period of participation in the study or for 3 months after administration of the study or reference drug in case of early termination of participation in the study.

Exclusion criteria

Severe chronic diseases, history of seizures;
Acute infectious diseases less than 4 weeks before administration of the study or reference drug;
Any history of chronic or recurrent infectious diseases;
History of tuberculosis;
Vaccination with any vaccine within 3 months before the administration of the study or reference drug or planned for the period of the volunteer's participation in the study;
Compounded allergy history; history of hypersensitivity to the active substance or other components of the study or reference drug;
Pregnancy or breastfeeding period;
Special lifestyle (work at night, extreme physical activity);
Deviations of vital signs: systolic pressure less than 100 mm Hg. Art. or more than 130 mm Hg. Art.; diastolic pressure less than 60 mm Hg. Art. or more than 90 mm Hg. Art.; heart rate less than 60 beats/min or more than 90 beats/min;
Dehydration due to diarrhea, vomiting, or other cause within 24 hours prior to administration of the study or reference drug;
Taking prescription medications within 28 days or 5 half-lives (whichever is longer) or taking over-the-counter medications/dietary supplements within 14 days prior to study or reference drug administration (occasional use of paracetamol at any time prior to study drug administration is acceptable) or reference drug);
Blood donation or blood loss (450 ml of blood or more) less than 3 months before the administration of the study or reference drug and/or blood donation in any quantity planned for the period of the volunteer's participation in the study;
Participation in clinical trials of medicinal products (less than 3 months or 5 half-lives from the study drug, whichever is longer) before administration of the investigational or reference drug of this study;
Regular alcohol consumption exceeding 5 units. alcohol per week (where each unit is equal to 30 ml of ethyl alcohol or 325 ml of beer), or information about a history of alcoholism, drug addiction, or drug abuse;
Positive test for the presence of alcohol in exhaled air;
Smoking more than 5 cigarettes per day for 3 months before this study;
Positive urine test for the content of narcotic and potent drugs;
Positive test for hepatitis B, C, HIV or syphilis;
Any surgical interventions planned during the period of participation in the study;
Unwillingness or inability to comply with the requirements of this protocol.