Roman Drai, MD, PhD, deputy director and head of clinical operations at Geropharm, discusses how Russia has developed its biopharmaceuticals industry.
Roman Drai, MD, PhD is the deputy director and head of clinical operations at Geropharm in St. Petersburg, Russia.
Transcript:
Can you tell us about the evolution of the Russian biopharmaceutical industry?
So, we had quite a good pharmaceutical industry back in the USSR, but in the 1990s, it was destroyed. In 2010, there was an initiative by our government called Pharma 2020. So, they started supporting biopharmaceutical companies, [including] some new biopharmaceutical companies. During these 10 years by 2020, we had to develop a certain amount of generics and biosimilars, and a certain amount of original drugs. And the support was by giving some grants to the pharmaceutical companies for clinical trials, because the main cost for the development of any drug is clinical trials, of course. I think that the program was successful, and that's why another program had been launched. [Well,] not had been launched but is launching at this time. [The government] decided to prolong [the program] by calling it Pharma 2030. And this Pharma 2030 will concentrate not on generics and biosimilars, but on original drugs. I would say that we really made a huge step, and now have become not only national leaders but we’re also trying to adopt international strategies. For example, Geropharm and some other companies, such as Biocon, [which is] already known in the world, and we started doing clinical trials abroad in Europe. And sometime, we will come to the United States, probably. So, I think that we have in our pipelines some good candidates, which will be first in class or best in class. And, let's see. I think that by 2030, we will have some blockbusters as well. So, we will compete with European and US manufacturing and pharmaceutical companies.
PBM Evolution Toward Value-Based Care Shifts to Transparent Pharmacy Pricing
March 30th 2025Josh Canavan, PharmD, RazorMetrics, and Chris O'Dell, Turquoise Health, predict pharmacy benefit managers (PBMs) will evolve toward value-based care, mirroring the broader shift toward open-cost structures.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Empowering Vulnerable Populations: The Path to Equitable Biologic Therapy Access
December 22nd 2024Elie Bahou, PharmD, senior vice president and system chief pharmacy officer at Providence, discusses strategies to improve equitable access to biologic therapies, including tiered formularies, income-based cost sharing, patient assistance programs, and fostering payer partnerships.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Can Global Policies to Boost Biosimilar Adoption Work in the US?
November 17th 2024On this special episode of Not So Different honoring Global Biosimilars Week, Craig Burton, executive director of the Biosimilars Council, explores how global policies—from incentives to health equity strategies—could boost biosimilar adoption in the US.
Q&A With Dr Chelsee Jensen: Navigating FDA Approvals, Challenges in the Biosimilar Landscape
January 14th 2024Chelsee Jensen, PharmD, BCPS, senior pharmacy specialist and pharmaceutical formulary manager at Mayo Clinic, reacts to the biggest FDA approvals of 2023 and how she sees the adalimumab, natalizumab, and tocilizumab spaces playing out.