Dose Escalation Study of the Pharmacodynamics, Pharmacokinetics, Safety, and Immunogenicity of BCD-132 in Patients With Relapsing-Remitting Multiple Sclerosis

Exclusion Criteria

• •Primary and secondary progressive multiple sclerosis;
• •Multiple sclerosis duration of more than 10 years with EDSS score ≤2.0 according to screening results;
• •Other conditions (except for multiple sclerosis) that can affect the assessment of multiple sclerosis symptoms: to mask, aggravate, change symptoms of multiple sclerosis, result in clinical signs or laboratory instrumental findings suggesting multiple sclerosis;
• •A relapse during the screening period;
• •Any acute infections, relapses of chronic infections or any other chronic diseases that are present on the day of signing informed consent and can, as judged by the Investigator, negatively affect the patient's safety during the study treatment;
• •HIV, hepatitis B, hepatitis C, or syphilis;
• •Metabolic abnormalities (disorders) manifesting as:
• •1. baseline creatinine levels increased more than 2-fold vs. upper limit of normal;
• •2. baseline urea levels increased more than 3-fold vs. upper limit of normal;
• •3. baseline ALT, AST or GGT levels increased more than 2.5-fold vs. upper limit of normal;
• •4. baseline bilirubin levels increased more than 1.5-fold vs. upper limit of normal;
• •Baseline leukocyte counts lower than \<3.0 × 10 9/L, platelet counts lower than \<125 × 10 9/L or hemoglobin levels \<100 g/L;
• •A history of severe depression, suicidal thoughts or suicide attempts;
• •Signs of clinical significant depression (baseline Beck's score of more than 15);
• •A history of hypothyroidism/hyperthyroidism and/or baseline abnormalities of TSH levels vs. lower or upper limits of normal;
• •Epilepsy;
• •Pregnancy, lactation or planned pregnancy over the entire study period;
• •A history of use
• •1. any time before signing informed consent: anti-B-cell agents (e.g., rituximab, ocrelizumab, abatacept, belimumab, ofatumumab, etc.);
• •2. any time before signing informed consent: alemtuzumab, anti-CD4 agents, daclizumab, teriflunomide, laquinimod, mitoxantrone, cladribine, total lymphatic irradiation, bone marrow transplant;
• •3. within 2 years (24 months) before signing informed consent: cyclophosphamide, cyclosporin, azathioprine; mycophenolate mofetil, fingolimod and other sphingosine-1-phosphate (S1P) receptor-modulating agents, natalizumab ;
• •4. therapy with immunoglobulin drug products within 12 weeks before signing informed consent.
• •Systemic corticosteroids used within 30 days before signing informed consent;
• •Hypersensitivity to any of BCD-132 ingredients;
• •Known alcoholic or drug dependency or signs of present alcoholic/drug dependence that, in the Investigator's opinion, can be contraindications for study therapy of multiple sclerosis with anti-CD20 monoclonal antibodies or limit treatment compliance;
• •Inability to follow the Protocol procedures (in the Investigator's opinion);
• •Contraindications to MRI or use of gadolinium-containing contrast agents:
• •1. Metal foreign objects in the body, magnetic implants, ferromagnetic clips for cerebral vessels, artificial heart valves, electronic middle ear implants, pacemakers;
• •2. A history of allergy to gadolinium or gadolinium-containing contrast agents;
• •с) Fear of cramped spaces; d) Kidney function impairment with a risk of delayed gadolinium elimination (creatinine level increased to more than 2 x upper limit of normal); e) Documented diagnosis of sickle cell or hemolytic anemia, hemoglobinopathy.
• •Any malignancies or a history of malignancies, except for cured basal cell carcinoma or cervical cancer in situ;
• •Vaccination within 6 weeks before signing informed consent (as told by the patient);
• •Participation in other clinical studies within 90 days before signing informed consent.