Special 5/2013

  • Biocapital

    In this issue:

    Good biocapital access – for a few

    In an era when payers are increasingly also looking at the economic benefits a new therapeutic has to offer, biotechs have to prove not only safety and efficacy to regulators, but cost-effectiveness to reimbursers as well. Both factors are subject to due dilligence when it comes time to apply for financing. That's why convincing investors of the value of product portfolios – which are most often developed by biotech innovators – has become a complex task. Market forecasts by Prime Therapeutics/Blue Cross-Blue Shield predict specialty drugs will account for 50% of all drug costs by 2018 (up from 20% in 2009). But the most current Global Biotech Report released by Ernst & Young at the end of April says despite that promising future, just a few large biotechs are benefiting from financing.

Volume 2014

Volume 2013

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http://www.european-biotechnology-news.com/magazine/spezial/2013/5/pos/1.html?cHash=f5f2e5fdbfbf799a701ac9c5e77ce04b&sort=desc

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