In an interview with the Center for Biosimilars, Venable’s Ha Kung Wong discusses concerns about “bad patents” hindering biosimilar access, but assures that the FDA and United States Patent and Trademark Office are working to improve the system. He discusses biosimilar cases to watch, including those for Eylea®, Soliris®, and Tysabri® biosimilars.
View the full interview “Biosimilars vs Bad Patents: Accessibility, Key Court Cases With Ha Kung Wong“ 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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