Venable partner Ha Kung Wong spoke at the ACI 10th Summit on Biosimilars as part of a panel that reviewed the economics of biosimilars and generic drugs. Highlights from his presentation comparing biosimilar markets in Europe and the United States and his take-home points for stakeholders were included in an article by the Center for Biosimilars. The article can be viewed here.
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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