2013
DOI: 10.1377/hlthaff.2009.0196
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Biosimilars And The European Experience: Implications For The United States

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Cited by 37 publications
(38 citation statements)
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“…This migration is happening quite effectively for nonspecialty drugs subject to competition from generic copies, but has not arrived in the US for most infused and oral biopharmaceuticals. This competition, and the resulting impact on unit prices, will only emerge when a sufficient number of therapeutically similar branded and biosimilar drugs become available for the major forms of cancer [11].…”
Section: Resultsmentioning
confidence: 99%
“…This migration is happening quite effectively for nonspecialty drugs subject to competition from generic copies, but has not arrived in the US for most infused and oral biopharmaceuticals. This competition, and the resulting impact on unit prices, will only emerge when a sufficient number of therapeutically similar branded and biosimilar drugs become available for the major forms of cancer [11].…”
Section: Resultsmentioning
confidence: 99%
“…As the leading region for the development of biosimilars, the experience of European uptake of biosimilars is being explored regularly for indications of how biosimilars will ultimately find their place in healthcare provision (Blackstone and Fuhr 2012;Grabowski, Guha, and Salgado 2014;Megerlin et al 2013). However, one fundamental question is how to assess uptake of a biosimilar: Is that as a share of its reference medicine, as a share of medicines of a similar 'vintage' of technology for a given indication or as a share of all medicines used for that indication?…”
Section: Mapping the Second Translational Gapmentioning
confidence: 99%
“…Biosimilars typically cost 25 percent less than comparable branded products in Europe and may enter the US market through the Food and Drug Administration's new regulatory approval pathway. 11 New firms are entering the global market for pharmaceuticals. Manufacturers in India, China, South Korea, and Israel are already proficient in manufacturing small-molecule generic drugs and are expanding their product development expertise to biosimilars.…”
Section: Design To Valuementioning
confidence: 99%