The Ministry of Health (MoH) of the Russian Federation has awarded Biocad marketing authorization for its interferon beta-1a biosimilar, a knockoff of Biogen’s Rebif® that is a key component in treatment of relapsing-remitting multiple sclerosis (RRMS) and included in all international recommendations and protocols. BIOCAD started the development program for interferon beta-1a biosimilar in 2012 and it took almost 5 years to run all the development phases, including pre-clinical/clinical studies and registration. The new biosimilar will be available for Russian patients already in 2017.
Today BIOCAD’s interferon beta-1a biosimilar is the only registered biosimilar of Rebif® in Russia and worldwide, which was developed in accordance with European Medicine Agency (EMA) guidelines. It showed no statistically meaningful difference in pharmacokinetics (PK) and pharmacodynamics (PD) parameters during phase I study and proved safety and efficacy equivalence to reference medicine in phase III study.
Included in the federal list of essential drugs and special reimbursement program for medicines used in rare debilitating diseases, interferon beta-1a is one of the most demanded therapeutic proteins the Russian government reimburses.
Roman Ivanov, the R&D vice-president of BIOCAD, said, “Interferon beta-1a biosimilar is the third authorized BIOCAD’s medicine for treatment of RRMS, which makes our biotechnological company the only manufacturer of both active pharmaceutical ingredients and drug products for all first generation disease-modifying therapies (DMTs). Moreover, 5 other drugs for use in MS, including 2 novel molecules, are in different development phases, supplementing the BIOCAD’s autoimmune diseases pipeline”.