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The Top 5 Biosimilars Articles for the Week of July 30
The Center for Biosimilars® recaps the top 5 articles for the week of July 30, 2018.
Transcript:
Hi, I’m Samantha DiGrande for The Center for Biosimilars®, your resource for clinical, regulatory, business, and policy news in the rapidly changing world of biosimilars.
Here are the top 5 biosimilars articles for the week of July 30.
Number 5: The Maine legislature has authorized a bill that seeks to combat the misuse of Risk Evaluation and Mitigation Strategy programs within the state.
Number 4: Mylan, together with partner Fujifilm Kyowa Kirin Biologics, has gained a positive opinion on its adalimumab biosimilar from the European Medicines Agency’s Committee for Medicinal Products for Human Use. Mylan plans to sell the drug under the brand name Hulio.
Number 3: England’s National Health Service reports strong savings from biosimilars so far, and says that, this financial year, it could save as much as 100 million pounds, equivalent to 131 million dollars, by using biosimilars.
Number 2: The European Commission has approved Pfizer’s trastuzumab biosimilar, Trazimera, referencing Herceptin, for marketing.
Number 1: Mylan, which in June received FDA approval for its biosimilar pegfilgrastim, Fulphila, has launched the drug in the US marketplace.
Finally, last week, our e-newsletter asked whether eventual marketing of the second filgrastim biosimilar will improve patient access.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Eye on Pharma: EU Aflibercept Approvals; Biosimilars Canada Campaign; Celltrion Data
November 19th 2024The European Commission grants marketing authorization to 2 aflibercept biosimilars; Biosimilars Canada launches new campaign to provide sustainable solutions to employers; Celltrion shares positive data for 2 biosimilars.
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.
Breaking Down Biosimilar Barriers: Interchangeability
November 14th 2024Part 3 of this series for Global Biosimilars Week, penned by Dracey Poore, director of biosimilars at Cardinal Health, explores the critical topic of interchangeability, examining its role in shaping biosimilar adoption and the broader implications for accessibility.
