drugset / Trial / NCT07597668
A Comparative Study of Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of RPH-035 and Ocrevus® in Patients With Relapsing-remitting or Secondary Progressive Multiple Sclerosis With Exacerbations
RandomizedParallel-groupDouble-blindTreatment
Summary
The study goal is to establish the equivalence of pharmacokinetic (PK) properties, as well as the comparability of safety, immunogenicity (IG) and pharmacodynamics (PD) of the drug product RPH-035 (R-Pharm JSC, Russia) in comparison with the drug product Ocrevus® (F. Hoffmann-La Roche Ltd., Switzerland) when used in patients with multiple sclerosis (MS)
Timeline
- Start
- 2025-04-16
- Primary completion
- 2026-06-02
- Completion
- 2027-11-24
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Ocrelizumab | Monoclonal antibody | 600 mg | — |
| Subject | RPH-035 | Unknown | 600 mg | Intravenous |