In an interview with the Center for Biosimilars, Venable’s Ha Kung Wong explores the challenges of “patent thickets” in the biologics market, where a complex web of patents can hinder development of more affordable biosimilar drugs. The discussion also highlights mechanisms to ensure fair competition and patient access.
View the full interview “Navigating the Patent Thicket: Balancing Innovation, Biosimilar Access in the Biologics Market” 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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