5 Things to Know About Biosimilars in the New Year
An update on where the field of biosimilars currently stands.
While the first biosimilar, Zarxio, was approved earlier this year, significant knowledge gaps exist with respect to clinical information on these follow-on biologicals, their interchageability, and potential impact on the economy. Here is where the field currently stands with respect to biosimilars:
Biosimilars and Their Impact on the Healthcare Economy
With a growing number of expensive biologicals entering the market across a broad range of therapeutic areas, payers and pharmacy benefit managers are exploring ways to curb the growing expense of biologicals, which sometimes cost more than 22 times that of small molecules. With the prediction that 80% of top-selling drugs in 2016 will be biologicals, biosimilars could be a saving grace for the economy,
FDA’s Suggestions for Naming Biosimilars
The first biosimilar is approved—but how do you name these products to ensure users are aware of the reference drug and interchangeability? With that objective, the FDA
Lack of Physician Awareness Could Hurt the Biosimilars Market
While physicians realize the clinical value and the economic impact of biosimilars, a new report suggests they lack the specific detailed information that would help them readily use these products in their practice. The
How Much Will Biosimilars Cost?
Novartis has finally marketed it’s biosimilar to Amgen’s Neupogen, but will Zarxio be priced much lower than the reference? And how would this reflect on the biosimilar pipeline that is under development? Read
Will Biosimilars Be Cost Effective? Payers Disagree
The introduction of biosimilars into the US market will not have a large impact on treatment costs until the volume of biosimilars for different therapies increases,
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