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IP and Antitrust Litigation in the Pharmaceutical Industry – Patent Infringement Lawsuit

by Ha Kung Wong
May 20, 2021

Venable’s Ha Kung Wong participated in a panel discussion of antitrust issues relating to IP litigations in the pharmaceutical industry.  This is the second webinar in a three-part series, discussing patent infringement lawsuits from the perspectives of innovators, generics, and biosimilars.  Topics include information on ANDAs, 502(b) applications, biosimilars and Paragraph IV notices; confidential access; Hatch-Waxman case timing, venue, court rules and mandatory disclosures; inducement of infringement; unlisted patents; and manufacturing patents.

View the LES Life Science webinar 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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