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Ha Kung Wong Discusses Antitrust Lawsuits on Increasing Biosimilar Accessibility with The Center for Biosimilars

by Ha Kung Wong
March 29, 2024

In an interview with the Center for Biosimilars, Venable’s Ha Kung Wong discusses lawsuits by drug companies aimed at delaying competition from biosimilars, including those involving Humira® (adalimumab) and Remicade® (infliximab) biosimilars, and the recent CareFirst BlueCross BlueShield involving delays for Stelara® (ustekinumab) biosimilars; but the effectiveness of these lawsuits in hindering biosimilar access remains uncertain.

View the full interview “Antitrust Lawsuits on Increasing Biosimilar Accessibility” 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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