{"id":3070,"date":"2021-08-05T15:03:00","date_gmt":"2021-08-05T20:03:00","guid":{"rendered":"https:\/\/patents.harnessip.com\/?p=3070"},"modified":"2021-08-14T11:45:40","modified_gmt":"2021-08-14T16:45:40","slug":"drug-labeling-that-excludes-patented-use-can-still-induce-infringement","status":"publish","type":"post","link":"https:\/\/patents.harnessip.com\/?p=3070","title":{"rendered":"Drug Labeling that Excludes Patented Use Can Still Induce Infringement"},"content":{"rendered":"\n<p>In <a href=\"http:\/\/www.cafc.uscourts.gov\/sites\/default\/files\/opinions-orders\/18-1976.OPINION.8-5-2021_1814836.pdf\">Glaxosmithkline LLC v. Teva Pharmaceuticals USA, Inc.<\/a>, [2018-1976, 2018-2023] (August 5, 2021), the Federal Circuit  vacated the grant of JMOL in favor of Teva, and reinstated the jury\u2019s verdict and damages award for infringement of RE40,000, and remanded for appropriate further proceedings. <\/p>\n\n\n\n<p>The \u2019000 patent claims a method of decreasing mortality caused by chronic heart failure by administering carvedilol with at least one other therapeutic agent.  <\/p>\n\n\n\n<p>Teva argued it could not have induced infringement prior to 2011, because it had \u201ccarved out\u201d the indication and prescribing information for treatment of congestive heart failure in its 2007 label under section viii, and that it could not be be liable for inducement for any time period because it did not cause others to infringe the method claimed in the \u2019000 patent.  The jury found the \u2019000 patent was not invalid, that Teva induced infringement of claims 1\u20133 during the partial label period proir to 2011, and that Teva induced infringement of claims 1\u20133 and 6\u20139 during the full label period after 2011. The jury assessed damages based on a combination of lost profits and a reasonable royalty and found Teva\u2019s infringement willful.<\/p>\n\n\n\n<p>The district court granted Teva\u2019s renewed motion for JMOL, finding that substantial evidence did not support the verdict of induced infringement because GSK failed to prove that Teva\u2019s alleged inducement, as opposed to other factors, actually caused physicians to directly infringe by prescribing generic carvedilol for the treatment of mild to severe chronic heart failure.<\/p>\n\n\n\n<p>The Federal Circuit agreed with GSK that substantial evidence supports that Teva actively<br>induced by marketing a drug with a label encouraging a patented therapeutic use. The Federal Circuit said that the labeling did not omit all patented indications or merely note (without mentioning any infringing uses) that FDA had rated a product as therapeutically equivalent to a brand-name drug.  Instead, the Federal Circuit said this was a case in which substantial evidence supports a jury finding that the patented use was on the generic label at all relevant times and that, therefore, Teva failed to carve out all patented indications. The Federal Circuit address the concerns of several amici, nothing that its narrow, case-specific review of substantial evidence does not upset the careful balance struck by the Hatch-Waxman Act regarding section viii carve-outs.<\/p>\n\n\n\n<p>35 U.S.C. \u00a7 271(b) provides \u201cWhoever actively induces infringement of a patent<br>shall be liable as an infringer.\u201dThe Federal Circuit explained that &#8220;[a] finding of inducement requires establishing \u201cthat the defendant possessed specific intent to encourage another\u2019s infringement.\u201d  This requires a plaintiff to show that the alleged infringer\u2019s actions induced infringing acts and that he knew or should have known his actions would induce actual infringements.  The Federal Circuit said that when a plaintiff relies on a drug\u2019s label accompanying the marketing of a drug to prove intent, the label must encourage,<br>recommend, or promote infringement.<\/p>\n\n\n\n<p>The Federal Circuit found that despite Teva&#8217;s purporting to carve out the patented congestive  heart failure indication, and its deletion of the indication from its pre-2011 partial label, substantial evidence supports the jury\u2019s finding that Teva induced doctors to infringe the method of use claimed in the \u2019000 patent. GSK argues that substantial evidence supports<br>the jury\u2019s verdict that Teva\u2019s partial label encouraged an infringing use (via the post-MI LVD indication) and that Teva\u2019s marketing materials encouraged prescribing carvedilol in a manner that would cause infringement of the \u2019000 patent, and the Federal Circuit agreed.  GSK provided substantial evidence that Teva\u2019s partial label instructed the method of use<br>claimed in the \u2019000 patent and thus was not a skinny label, because some of the labeled incidations overlapped the patented process.<\/p>\n\n\n\n<p>  <\/p>\n","protected":false},"excerpt":{"rendered":"<p>In Glaxosmithkline LLC v. Teva Pharmaceuticals USA, Inc., [2018-1976, 2018-2023] (August 5, 2021), the Federal Circuit vacated the grant of JMOL in favor of Teva, and reinstated the jury\u2019s verdict and damages award for infringement of RE40,000, and remanded for &hellip; <a href=\"https:\/\/patents.harnessip.com\/?p=3070\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[27],"tags":[],"class_list":["post-3070","post","type-post","status-publish","format-standard","hentry","category-inducement"],"post_mailing_queue_ids":[],"_links":{"self":[{"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=\/wp\/v2\/posts\/3070","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=3070"}],"version-history":[{"count":1,"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=\/wp\/v2\/posts\/3070\/revisions"}],"predecessor-version":[{"id":3071,"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=\/wp\/v2\/posts\/3070\/revisions\/3071"}],"wp:attachment":[{"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=3070"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=3070"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/patents.harnessip.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=3070"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}