NCT07321093Toboroz3. fázis
A Study of the Efficacy and Safety of BCD-281 in Patients With Relapsing-Remitting Multiple Sclerosis
A Double-blind, Randomized Clinical Study of the Efficacy and Safety of BCD-281 in Patients With Relapsing-Remitting Multiple Sclerosis
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. jan. 6.
Rövid összefoglaló (regiszter, angolul)
The aim of this study is to compare the efficacy, safety profile, pharmacokinetics, pharmacodynamics, and immunogenicity of BCD-281 and the reference drug in subjects with relapsing multiple sclerosis.
- Állapot (regiszter)
- Toboroz
- Fázis (regiszter)
- 3. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 292 (tervezett)
- Első benyújtás
- 2025. nov. 17.
- Kezdés
- 2025. nov. 1.
- Elsődleges befejezés
- 2028. dec.
- Fő szponzor
- Biocad
- Betegségek
- Sclerosis multiplex (SM)
- NCT-szám
- NCT07321093
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 3. fázis
- Tervezett résztvevők: 292
- 2025. nov. 1. és az elsődleges befejezés (2028. dec.) között
- 1 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
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Korábbi kezelés
- Any comorbidities requiring treatment with systemic glucocorticoids and/or immunosuppressive drugs for the duration of the study, with the exception of MS.
- Concomitant diseases and/or conditions that may affect the assessment of the clinical picture of the underlying disease and/or significantly increase the risk of AEs during the study.
- Known alcohol or drug addiction, or current signs of alcohol/drug addiction.
- History of a malignant disease within 5 years prior to screening.
Más betegség
- Malignant form of MS.
- Other medical conditions that can affect the assessment of clinical picture of the MS.
- History of progressive multifocal leukoencephalopathy.
- Any acute or exacerbated chronic infections detected during screening that may have a negative impact on subject's safety during the study therapy.
- History of severe depression and/or a Beck Depression Inventory score of ≥16 at screening examination.
- A diagnosis of HIV infection, hepatitis B or C .
- A history of severe allergic or anaphylactic reactions to humanized and/or murine monoclonal antibodies.
- A history of using any prohibited medications or treatments defined in the study protocol.
Laborértékek
- Abnormal laboratory blood values, as specified in the study protocol.
Egyéb
- Primary progressive or secondary progressive MS.
- MS duration of more than 10 years with EDSS score of ≤2.0 at screening.
- Inability to obtain high-quality MRI images and/or the presence of contraindications to MRI and the administration of gadolinium-containing contrast agents.
- Inability to provide the subject with venous access.
- Pregnancy or breastfeeding, pregnancy planning and oocyte donation throughout the study and for 5 months after the last dose of ocrelizumab.
Kiket keres a vizsgálat
- Provided written ICF to participate in the study.
- Male and female subjects aged 18 to 55 years inclusive at the time of signing the ICF.
- Diagnosis of multiple sclerosis, established in accordance with the McDonald criteria for the diagnosis of multiple sclerosis (2017 revision).
- Relapsing-remitting multiple sclerosis.
- The total EDSS score 0-5.5 inclusive.
- Documentary evidence of the following at the time of signing the ICF:
- at least one relapse within the last12 months, and/or
- 2 relapses within the last 24 months, and/or
- at least 1 T1 Gd+ lesion detected on brain MRI and 1 relapse within 24 months prior to signing the ICF.
- Presence of IgG antibodies to the Varicella-Zoster virus.
- Neurological stability for 30 days prior to signing the ICF.
- Subject's willingness to discontinue previously prescribed DMTs from the day of the first administration of the IP and throughout the study.
- The ability of the subject to follow the Protocol procedures, according to the Investigator.
- Willingness of subjects of both sexes and their sexual partners of childbearing potential to use reliable methods of contraception from the time of signing ICF, throughout the study and for 5 months after the last dose of the drug in this study.
Életkor a regiszterben: 18 év – 55 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (1)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| LLC "Medis" | Nizhny Novgorod | Oroszország | Toboroz |
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