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

NCT07597668

Phase 1 Active not recruiting 180 enrolled R-Pharm
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

EvaluationDrugModalityDoseRoute
Comparator Ocrelizumab Monoclonal antibody 600 mg
Subject RPH-035 Unknown 600 mg Intravenous

Indications