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Increased Affordability and Patient Access

Since Hospira launched its biosimilars, prices have decreased and patient access has increased.

In Europe and Australia, biosimilar treatments offer cost savings to healthcare systems of approximately 25 percent to 30 percent.1 In the United States, newer biologic treatments can cost $100,000 or more per patient, per year.2 A price decrease in the United States similar to the one experienced in Europe would benefit patients and payers alike.

A number of studies predict that successful adoption of biosimilars in the United States could result in significant savings for U.S. patients and the U.S. healthcare system driven by increased competition. A 2013 study by accounting firm Grant Thornton found that biosimilars hold the potential to save $20 billion annually in the United States.3

Market Penetration of Biosimilars and U.S. Market Formation

With the continued safe and effective record of biosimilars in European Union clinical practice, use in many markets is widespread and growing rapidly. Throughout the European Union, biosimilar versions of GCSF had gained almost 41 percent of the total daily GCSF market by the end of 2012, up from 30 percent at the start of the year.4 During the same period, EPO biosimilars had grown their market share to 19 percent of the European short-acting EPO market, up from 15 percent at the beginning of 2012.5

"Biosimilars have come to stay in Europe, and we're very pleased with the progress we are seeing," Hospira's Moore said. "European and Australian physicians trust in the safety, efficacy and quality of biosimilars for their patients."

 

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