Analysis of biosimilars: Finding the relevant needles in a haystack

• In: S5 - Biosimilars (part II): From science to practice on Wednesday, 3 September 2008, 14:00-17:00
• At: Basel (Switzerland) (2008)
• Type: Presentation
• By: VAN DE WEERT, Marco (University of Copenhagen, Copenhagen, Denmark)
• Abstract:

  Market approval of most generic medicines requires the generic manufacturer to show bioequivalence to the innovator drug. While a similar approach would be desired for biosimilar proteins, their highly complex behaviour makes this impossible. In particular, the danger of invoking an immune response is a special feature of protein drugs, and this

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