On May 13, 2015, a divided Federal Circuit panel, on remand from the United States Supreme Court, affirmed a district court finding of no direct infringement under 35 U.S.C. § 271(a), because a defendant did not perform all steps of the asserted method claims, and the actions of its customers who carried out the remaining steps could not be attributed to defendant.
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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