drugset / Trial / NCT02727907

Study of Efficacy and Safety of Drugs BCD-033 and Rebif for Treatment of Patients With Multiple Sclerosis

NCT02727907

Phase 2/3 Completed 163 enrolled Biocad
RandomizedParallel-groupQuadruple-blindOther

Summary

Study design is double-blind, randomized, placebo-controlled study in 3 parallel groups with the use of active comparator and placebo. Total duration of therapy of about 2 years. Study hypothesis is equivalence of efficacy and safety of the investigational drug BCD-033 original drug Rebif®.

Timeline

Start
2015-02-12
Primary completion
2016-11-21
Completion
2017-08-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Interferon beta-1a Protein / enzyme biologic 44 ug Subcutaneous

Indications