Venable Fizpatrick partner Ha Kung Wong spoke with Law360 for an article about Amgen v. Sanofi, a case currently pending at the Federal Circuit involving patents related to the biologic drugs Praluent and Repatha. At issue in this case is whether patents claiming a genus of antibodies meet the enablement requirement. Numerous companies, including Bristol-Myers Squibb, Merck, Eli Lilly, and Pfizer have filed amicus briefs.
The article by Law360 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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