federal circuit review | september 2012

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VOLUME 2 | ISSUE 9 SEPTEMBER 2012 Hatch-Waxman Safe Harbor Extends to Information-Gathering Activities In Momenta Pharmaceuticals, Inc. v. Amphastar Pharmaceuticals, Inc. (Docket No. 2012-1062), the Federal Circuit vacated a preliminary injunction for applying an “unduly narrow interpretation” of the Hatch-Waxman safe harbor, 35 U.S.C. § 271(e)(1). Momenta, assignee of a patent relating to methods for analyzing enoxaparin, brought suit alleging that Amphastar infringed the claimed methods during quality control batch testing of its commercial enoxaparin product. Amphastar argued that its activity fell within the § 271(e)(1) safe harbor, as the testing was required by the FDA for continued approval and sale of its product. The district court disagreed, and issued a preliminary injunction. The Federal Circuit reversed, holding that the safe harbor of § 271(e)(1) is not limited to ANDA filings, but rather applies to both pre- approval and post-approval information-gathering activities “[a]s long as the allegedly infringing use is ‘for uses reasonably related’ to the development and submission of that information . . . .Amphastar’s post-approval quality testing was in accordance with FDA regulations requiring the maintenance of batch records that “shall be readily available” for inspection by the FDA. The Federal Circuit held that the possibility of FDA inspection was sufficient to constitute “submission” of the records to the FDA under § 271(e) (1). The availability of non-infringing methods to meet the FDA’s requirements was not relevant. Judge Rader dissented, arguing that the statute was ambiguous, and based on the legislative history and precedent such as Classen Immunotherapies, Inc. v. Biogen IDEC, 659 F.3d 1057 (Fed. Cir. 2011), Eli Lilly & Co. v. Medtronic Inc., 496 U.S. 661 (1990), and Merck KGaA v. Integra Lifesciences I, Ltd., 545 U.S. 193 (2005), Judge Rader concluded that § 271(e)(1) only applies to pre- marketing approval activities. Patent Invalid for Lack of Enablement in Light of “At Least 10%” Limitation In Magsil Corp. v. Hitachi Global Storage Technologies, Inc. (Docket No. 2011-1221), the Federal Circuit affirmed the district court’s grant of summary judgment of invalidity for lack of enablement. In This Issue Hatch-Waxman Safe Harbor Extends to Information-Gathering Activities Patent Invalid for Lack of Enablement in Light of “At Least 10%” Limitation Isolated DNA Is Patent Eligible Subject Matter Recapture Rule Clarified • Liability for Induced Infringement Can Occur Even if No Single Actor Is a Direct Infringer

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The Federal Circuit Review is a monthly newsletter featuring the latest case summaries handed down from the U.S. Court of Appeals for the Federal Circuit.

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Page 1: Federal Circuit Review | September 2012

Federal Circuit Review

VOLUME 2 | ISSUE 9 SEPTEMBER 2012

Hatch-Waxman Safe Harbor Extends to Information-Gathering ActivitiesIn Momenta Pharmaceuticals, Inc. v. Amphastar Pharmaceuticals, Inc. (Docket No. 2012-1062), the Federal Circuit vacated a preliminary injunction for applying an “unduly narrow interpretation” of the Hatch-Waxman safe harbor, 35 U.S.C. § 271(e)(1). Momenta, assignee of a patent relating to methods for analyzing enoxaparin, brought suit alleging that Amphastar infringed the claimed methods during quality control batch testing of its commercial enoxaparin product. Amphastar argued that its activity fell within the § 271(e)(1) safe harbor, as the testing was required by the FDA for continued approval and sale of its product. The district court disagreed, and issued a preliminary injunction. The Federal Circuit reversed, holding that the safe harbor of § 271(e)(1) is not limited to ANDA filings, but rather applies to both pre-approval and post-approval information-gathering activities “[a]s long as the allegedly infringing use is ‘for uses reasonably related’ to the development and submission of that information . . . .” Amphastar’s post-approval quality testing was in accordance with FDA regulations requiring the maintenance of batch records that “shall be readily available” for inspection by the FDA. The Federal Circuit held that the possibility of FDA inspection was sufficient to constitute “submission” of the records to the FDA under § 271(e)(1). The availability of non-infringing methods to meet the FDA’s requirements was not relevant. Judge Rader dissented, arguing that the statute was ambiguous, and based on the legislative history and precedent such as Classen Immunotherapies, Inc. v. Biogen IDEC, 659 F.3d 1057 (Fed. Cir. 2011), Eli Lilly & Co. v. Medtronic Inc., 496 U.S. 661 (1990), and Merck KGaA v. Integra Lifesciences I, Ltd., 545 U.S. 193 (2005), Judge Rader concluded that § 271(e)(1) only applies to pre-marketing approval activities.

Patent Invalid for Lack of Enablement in Light of “At Least 10%” LimitationIn Magsil Corp. v. Hitachi Global Storage Technologies, Inc. (Docket No. 2011-1221), the Federal Circuit affirmed the district court’s grant of summary judgment of invalidity for lack of enablement.

In This Issue• Hatch-Waxman Safe Harbor Extends to Information-Gathering Activities

• Patent Invalid for Lack of Enablement in Light of “At Least 10%” Limitation

• Isolated DNA Is Patent Eligible Subject Matter

• Recapture Rule Clarified

• Liability for Induced Infringement Can Occur Even if No Single Actor Is a Direct Infringer

Page 2: Federal Circuit Review | September 2012

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MagSil filed suit against Hitachi alleging that Hitachi’s disk drive products infringe MagSil’s patent. After claim construction, the district court granted summary judgment of invalidity for lack of enablement. The Federal Circuit affirmed, concluding that Hitachi had provided clear and convincing evidence that one of skill in the art could not have taken the disclosure in the specification and achieved the full scope of the claims. The asserted claims broadly claim a tunnel junction that “causes a change in the resistance by at least 10% at room temperature.” The Federal Circuit determined that the open ended claim language of “at least 10%” covered all changes from 10% to infinity and that the specification could not enable such broad claim language. The Federal Circuit found that the specification only disclosed enough information to achieve an 11.8% resistance change and that, during prosecution, MagSil believed the highest possible resistive change to be 100%. The Federal Circuit concluded that the specification only enabled a person of ordinary skill in the art to achieve a small subset of the claimed range and that the record contained no evidence that a skilled artisan could use the specification to achieve the modern values of 600% change in resistance without undue experimentation.

Isolated DNA Is Patent Eligible Subject MatterIn Association For Molecular Pathology v. U.S. Patent And Trademark Office (“MYRIAD”) (Docket No. 2010-1406), the Federal Circuit maintained its previous holding that composition claims to isolated DNA molecules cover patent-eligible subject matter. Plaintiffs sought declaratory judgment of invalidity of certain claims of Myriad’s patents. The district court found that composition claims to isolated DNA molecules were patent-ineligible subject matter under 35 U.S.C. § 101. The Federal Circuit reversed this holding in an earlier decision. The Supreme Court remanded the case to the Federal Circuit for reconsideration in light of Mayo Collaborative Services v. Prometheus Laboratories, Inc., 132 S. Ct. 1289 (2012). The Federal Circuit maintained its previous decision with regard to the patent-eligibility of isolated DNA molecules. Like the prior decision, the Federal Circuit found that “the distinctive nature of DNA molecules as isolated compositions of matter” renders them patent eligible subject matter. Specifically, the Federal Circuit found that the chemical structure of the isolated DNA in question renders it “markedly different” from naturally occurring DNA. The Federal Circuit rejected the argument that the physiological use or benefit of the DNA is necessarily relevant to patent eligibility analysis. In reaching its decision, the Federal Circuit stated that, “[w]hile Mayo . . . provide[s] valuable insights and illumate[s] broad, foundational principles, the Supreme Court’s decisions in [Diamond v. Chakrabarty, 447 U.S. 303 (1979)] and Funk Brothers [Seed Co. v. Kalo Inoculant Co., 333 U.S. 127 (1948)] set out the primary framework for deciding the patent eligibility of compositions of matter, including isolated DNA molecules.” In addition, in line with its prior decision, the Federal Circuit affirmed the district court’s holding that jurisdiction existed under the Declaratory Judgment Act, reversed the district court’s holding that method claims to screening via cell growth rates is patent-ineligible subject matter and affirmed the district court’s holding that method claims directed to comparing or analyzing gene sequences is patent-ineligible subject matter. Judge Bryson dissented with respect to the composition claims to isolated DNA molecules, arguing that the altered chemical structure of the isolated DNA was a result of the isolation process, and did not render the compositions patent eligible. Rather, he argued that, under Chakrabarty, the similarity in structure as well as in utility between the claimed isolated DNA and the naturally occurring DNA rendered the claimed composition patent-ineligible as a naturally occurring substance.

Recapture Rule ClarifiedIn Greenliant Systems, Inc. v. Xicor LLC (Docket No. 2011-1514), the Federal Circuit affirmed the grant of a declaratory judgment holding reissue claims invalid under the rule against recapture. Greenliant filed a declaratory judgment seeking a declaration that Xicor’s reissue claims are invalid and not infringed. The district court entered a judgment in favor of Greenliant that certain claims of the patent are invalid under the recapture rule. The Federal Circuit affirmed. In addressing whether a patentee surrendered subject matter in the original prosecution which is encompassed by broadened reissue claims, the focus is on arguments actually made by the patentee: “It does not matter whether the examiner or the Board adopted a certain argument for allowance; the sole question is whether the argument was made [by the applicant].” Thus, the Federal Circuit rejected Xicor’s argument that there was no disclaimer of the subject matter because its arguments were not persuasive to the Examiner or the Board. Rather, the Federal Circuit found that Xicor clearly and unmistakably represented to the Examiner and the BPAI that the relevant subject matter was a necessary component that imparted features distinguishing the claimed subject matter over prior art during the original prosecution. Thus, the patentee was not allowed to recapture the broader subject matter that it had given up.

Page 3: Federal Circuit Review | September 2012

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Liability for Induced Infringement Can Occur Even if No Single Actor Is a Direct InfringerIn Akamai Technologies, Inc. v. Limelight Networks, Inc. (Docket No. 2009-1372), the Federal Circuit reversed two district courts’ granting of summary judgment and JMOL for defendants.In reviewing two district court decisions, Akamai Technologies, Inc. v. Limelight Networks, Inc. and McKesson Technologies, Inc. v. Epic Systems Corp., the Federal Circuit examined whether a defendant may be held liable for induced infringement if no single party has performed all of the steps of a patented method, but the defendant has induced others to act such that all method steps have been performed.In Akamai, Limelight performed all steps of Akamai’s patented method of efficient delivery of web content, except a step of modifying a content provider’s web page to reference particular servers. Limelight provided instructions on how to perform that step to its customers, some of which elected to perform the step. In McKesson, Epic Systems sold software to healthcare providers, which used the software to communicate electronically with patients. Epic Systems did not perform any steps of McKesson’s patented method, but those steps were practiced by a combination of the healthcare providers and the patients when Epic’s product was used as intended. In both cases, the lower court found that no single entity directly infringed, and thus there could be no inducement of infringement.The en banc Federal Circuit expressly overruled BMC Resources, 498 F.3d 1373 (Fed. Cir. 2007), which required that, in order for a party to be liable for induced infringement, some other single entity must be liable for direct infringement. The Federal Circuit held that, while all the steps of a claimed method must be performed to find induced infringement, “it is not necessary to prove that all the steps were committed by a single entity.” Thus, the requirement that inducement gives rise to liability only if the inducement leads to actual infringement remains. However, the Federal Circuit distinguished between the concept of direct infringement, and liability for direct infringement: “Requiring proof that there has been direct infringement as a predicate for induced infringement is not the same as requiring proof that a single party would be liable as a direct infringer.” “If a party has knowingly induced others to commit the acts necessary to infringe the plaintiff’s patent and those others commit those acts, there is no reason to immunize the inducer from liability for indirect infringement” simply because no single defendant is liable for direct infringement. A party that induces several actors to collectively practice the patented method should be treated the same as a party that induces a single actor to practice the patented method. The impact on the patentee is the same. Thus, “infringement” in the context of 35 U.S.C. § 271(b) refers to “the acts necessary to infringe a patent, not to whether those acts are performed by one entity or several.” The Federal Circuit found this reasoning consistent with the legislative history of the 1952 Patent Act, and liability principles in other areas of law such as tort and criminal law. In so holding, the Federal Circuit expressly declined to revisit any of the principles regarding the law of divided infringement as it applies to liability for direct infringement under 35 U.S.C. § 271(a).In remanding McKesson and Akamai, the Federal Circuit advised that Epic and Limelight may be liable for induced infringement by showing (1) they knew of the patent; (2) they either induced the performance of all of the method steps, or performed some steps and induced performance of the remaining steps; and (3) all the steps were performed.Judge Newman filed a dissent, arguing that inducement under § 271(b) should require an underlying act of infringement for which a party is liable under § 271(a), but would have overturned earlier opinions requiring a single infringer for direct infringement, instead looking to apportionment of damages in cases of divided infringement.Judge Linn filed a dissent joined by Judges Dyk, Prost, and O’Malley, arguing that liability under § 271(b) requires an act of infringement under § 271(a) by a single entity or joint enterprise.

Page 4: Federal Circuit Review | September 2012

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© 2012 Knobbe Martens Olson & Bear LLP, a Limited Liability Partnership including Professional Corporations. All rights reserved. The information contained in this newsletter has been prepared by Knobbe, Martens, Olson & Bear, LLP and is for general informational purposes only. It does not constitute legal advice. While every effort has been made to ensure the accuracy of the information contained in this newsletter, Knobbe Martens Olson & Bear LLP does not guarantee such accuracy and cannot be held liable for any errors in or any reliance upon this information. Transmission of this newsletter is neither intended nor provided to create an attorney-client relationship, and receipt does not constitute an attorney-client relationship. You should seek professional counsel before acting upon any of the information contained in this newsletter.

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