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centerforbiosimilars
5 小时
IRA Reimbursement Impact on Biosimilars Minimal Despite Rising Market Share
The Inflation Reduction Act (IRA) has modestly boosted oncology biosimilar uptake through Medicare reimbursement, but its ...
centerforbiosimilars
23 小时
BioRationality—The Missing Rationality in Biosimilar Discussions and the Path Forward
The article by Sarfaraz K. Niazi, PhD, critiques the irrationality surrounding biosimilars, suggesting that regulatory ...
centerforbiosimilars
1 天
AAM Report: Despite Massive Savings, Patient OOP Costs on Biosimilars, Generics Remain High ...
Part 2 of our series diving into the Association for Accessible Medicines' (AAM) latest report discusses that while generics ...
centerforbiosimilars
1 天
Skylar Jeremias
Part 2 of our series diving into the Association for Accessible Medicines' (AAM) latest report discusses that while generics and biosimilars saved $445 billion in 2023, their potential is hindered by ...
centerforbiosimilars
7 天
AAM Report: Generics and Biosimilars Savings Reach $445 Billion in 2023, Part 1
Savings from generic and biosimilar drugs totaled $445 billion in 2023, showing promise for the growth of both markets and ...
centerforbiosimilars
5 天
The Top 5 Biosimilar Articles for the Week of September 16
Number 5: The FDA has approved Pavblu (aflibercept-ayyh), the fifth biosimilar referencing Eylea (aflibercept).1 The new ...
centerforbiosimilars
9 天
STADA Credits Biosimilar Expansion for Profitable First Half of 2024
German biosimilar manufacturer STADA Arzneimittel reported a 9% revenue increase in the first half of 2024, with over €2 ...
centerforbiosimilars
8 天
Expanding Biosimilar Adoption: Insights and Strategies With Dr Sophia Humphreys
Sophia Humphreys, PharmD, MHA, BCBBS, director of system formulary management at Sutter Health, discusses the challenges of ...
centerforbiosimilars
15 天
Patients With nAMD Successfully Switch From Aflibercept to Ranibizumab
A study found patients with neovascular age-related macular degeneration (nAMD) successfully switched from aflibercept to the ...
centerforbiosimilars
8 天
FDA Approves Pavblu for Retinal Conditions
Amgen’s Pavblu (aflibercept-ayyh) is the fifth biosimilar referencing Eylea (aflibercept) to be approved for American ...
centerforbiosimilars
14 天
The Future of Biosimilar Gene Therapies: Key Issues and Potential
While biosimilars could potentially lower costs and improve access to gene therapies, significant hurdles in regulation, ...
centerforbiosimilars
16 天
BioRationality: FDA Clarification Provides New Indications and Process Change for Biosimilars
Sarfaraz K. Niazi, PhD, explains the FDA's new guidelines on post-approval changes for biosimilars, emphasizing the processes ...
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