Multiple Sclerosis
Conditions
Brief summary
Clinical study BCD-132-4/MIRANTIBUS is an international, multicenter, randomized, double-blind, double-masked study using an active reference drug (teriflunomide). The goal of the study is to evaluate the efficacy and safety of BCD-132 in the treatment of patients with relapsing multiple sclerosis.
Detailed description
Clinical study No. BCD-132-4/MIRANTIBUS is an international, multicenter, randomized, double-blind, double-masked study using an active reference drug (teriflunomide). The goal of the study is to evaluate the efficacy and safety of BCD-132 in the treatment of patients with relapsing multiple sclerosis. The study includes adults with relapsing-remitting multiple sclerosis (according to 2017 revision to the McDonald Diagnostic Criteria for Multiple Sclerosis) and EDSS disability score up to 5.5. Some of the subjects in this study will be patients rolled over from ongoing phase II clinical study No. BCD-132-2; treatment group, individual product kit number (IPKN), stratification factors, order of procedures and timeframes for blinded therapy with a duration of up to 100 weeks will remain the same.
Interventions
BIOLOGICALBCD-132
anti-CD20 monoclonal antibody
DRUGTeriflunomide
Teriflunomide 14 mg
Sponsors
Biocad
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No
Inclusion criteria
1. Written informed consent for participation in the study; 2. Male and female subjects, 18 to 60 years of age 3. Diagnosis of relapsing multiple sclerosis (according to 2017 revision to the McDonald Diagnostic Criteria for Multiple Sclerosis); 4. Documentary evidence that, at the time of signing the informed consent, the subject had: 1. at least 1 relapse within the last calendar year (12 months), or 2. 2 relapses within the last 2 years (24 months), or 3. at least 1 T1 gadolinium-enhanced brain lesion on MRI and 1 relapse within 2 calendar years (24 months) prior to signing the informed consent; 5. The subject must be neurologically stable for 30 days prior to signing the informed consent 6. Total EDSS score 0 to 5.5 inclusive 7. Positive anti-Varicella Zoster IgG antibodies according to screening test results; 8. Absence of suicidal ideation and behavior confirmed at screening according to C-SSRS score within 1 month prior to signing the informed consent 9. Willingness of both female and male patients and their sexual partners of childbearing potential to use reliable contraception
Exclusion criteria
Primary progressive MS; Duration of multiple sclerosis for more than 10 years with EDSS ≤2.0 according to screening assessments; Other disorders (besides multiple sclerosis), which could affect the assessment of symptom severity for the primary disease A relapse during screening period ; Use of systemic corticosteroids for 30 days prior to signing the informed consent; Disorders, besides multiple sclerosis, requiring long-term systemic therapy with corticosteroids and/or immunosuppressants; Heart failure (NYHA functional class III/IV); encephalopathy, lactic acidosis, MELAS syndrome), neuromyelitis optica, sarcoidosis; Diagnosis of HIV, hepatitis B, hepatitis C, or syphilis ; Increased TTG levels at least two times the upper limit of normal on screening tests; Suicidal ideation and/or behavior History of severe depression Pregnancy, breastfeeding, or intention to become pregnant at any point throughout the study period; Prior use of anti-B cell therapies Intolerance, including hypersensitivity to any component of BCD-132/teriflunomide, premedication drugs, or conditions in which the above drugs are contraindicated in the Investigator's opinion; History of severe allergic or anaphylactic reactions to humanized and/or murine monoclonal antibodies; History of progressive multifocal leukoencephalopathy Known alcohol or drug addiction or signs of current alcohol/drug addiction Inability to follow the procedures specified in the Protocol, as assessed by the Investigator; Contraindications to MRI and administration of gadolinium-based contrast agents: Any current or prior malignancies, except for successfully treated basal cell carcinoma and cervical carcinoma in situ Vaccination within 6 weeks prior to signing the informed consent \-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Annualized relapse rate | week 48 | Annualized relapse rate at 48 weeks after the randomization of the last patient in the study |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Total number of T1 Gd+ lesions | week 48 | Total number of T1 Gd+ lesions (per scan) detected on brain MRI; |
| CUA | week 48 | Combined unique active lesions |
| Proportion of patients without contrast-enhancing lesions | week 48 | Proportion of patients without contrast-enhancing lesions |
| Number of new or enlarged T2 lesions | week 48 | Number of new or enlarged T2 lesions |
| Proportion of patients with persistent progression | week 48 | Persistent progression is defined as an increase in the EDSS score from Visit 1 by at least 1.0 in patients with a score \>0 and ≤5.5 at the first visit and by at least 1.5 in patients with a score of 0 at the first visit |
| Changes in the neurologic deficit according to EDSS score | week 48 | Changes in the neurologic deficit according to Expanded Disability Status Scale |
| Annualized relapse rate | week 48 | Mean annualized relapse rate |
| Proportion of patients with adverse reactions | week 48 | — |
| Proportion of patients with serious adverse reactions | week 48 | — |
| Proportion of patients without new or enlarged T2 lesions | week 48 | Proportion of patients without new or enlarged T2 lesions |
Countries
Russia
Outcome results
None listed