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No uniform everyday supply of biosimilars

Biopharmaceuticals have become an integral part of the drug therapy of many diseases. With increasing sales in this market, biopharmaceuticals are responsible for a significant portion of statutory health insurance drug expenditure. For this reason, the timely market launch of biosimilars after the patent expiry of the original preparations is of crucial importance. Biosimilar manufacturers and various health insurance companies have great interest in steadily and comprehensively increasing the biosimilar market share. The analysis by INSIGHT Health shows that care in Germany is not uniform.

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First publication date: 04.06.2014

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>> In the market segment of genetically engineered drugs, 114 active ingredients are currently approved (see vfa, as of June 6, 2014, although biosimilars with the same name are not counted as new active ingredients here, unlike the vfa). There are only biosimilars from different providers on the market for five of these 114 active ingredients. The analysis looks at the three top-selling active ingredients or active ingredient groups: biosimilar epoetins (epoetin alfa and zeta), filgrastim and somatropin. For the latter two biopharmaceuticals filgrastim and somatropin, further copycat products were approved in 2013, after there had been no biosimilar approvals at all in 2011 and 2012 (see vfa, “Medical Biotechnology in Germany 2014”).
In addition to the three active ingredients/groups of active ingredients already mentioned, biosimilars for follitropin alfa and infliximab are approved.

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Citation information: doi: 10.24945/MVF.04.14.1866-0533.1949

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