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How Can Biosimilars Make Headway in the U.S. Market?

by Ha Kung Wong
June 26, 2019

Venable partner Ha Kung Wong spoke at ISPOR’s annual conference as part of a panel that discussed the biosimilar market in the US.  As a follow-up to that presentation, Ha Kung participated in a Q&A for Biosimilar Development, including providing thoughts on:

  • What we have learned from the biosimilar experience in Europe and implications for biosimilar hurdles in the U.S.
  • The greatest market access hurdles/challenges to overcome in the biosimilars field within the U.S. market and what could be done to address these challenges
  • Key areas for improvement within the biosimilar industry

The article can be viewed here.

    Methodology

    Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.

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