• ABAThe American Bar Association (ABA) Section of Intellectual Property Law, Young Lawyers Division, and Center for Continuing Legal Education will be offering a live webinar and teleconference entitled "Understanding the America Invents Act: A Sweeping Change of U.S. Patent Prosecution Practice" on June 1, 2012 from 1:00 – 2:30 pm (EDT).  Donna Meuth, Senior Patent Counsel, Intellectual Property for Eisai Inc. will moderate a panel including Robert W. Bahr of the U.S. Patent and Trademark Office; Thomas L. Irving of Finnegan, Henderson, Farabow, Garrett & Dunner, LLP; Teresa Stanek Rea, Deputy Director of the U.S. Patent and Trademark Office; and MaCharri Vondran-Jones, Counsel, Patent Division for Eli Lilly and Company.  The panel will examine how the AIA will impact different aspects of patent prosecution before the USPTO and discuss strategies for implementing those changes.  In particular, the panel will discuss the change to first-inventor-to-file and accompanying changes to the definition of prior art, and the new Supplemental Examination procedure, and provide strategic advice regarding best practices.

    The registration fee for the webcast is $95 for members of any of the sections sponsoring the webinar, $99 for government attorneys, $150 for ABA members, and $195 for the general public.  Those interested in registering for the webinar, can do so here or by calling 800-285-2221.

  • By Kevin E. Noonan

    BaxterIn a dissent from the Federal Circuit's affirmance of a Board determination of obviousness, Judge Newman raises a jurisdictional and separation-of-powers argument in In re Baxter International, Inc. that is destined to be decided by the Supreme Court.  Specifically, what power does the U.S. Patent and Trademark Office have to determine that a patent is invalid in a re-examination concluded after the Federal Circuit determines that the patent is not invalid after challenge during patent infringement litigation on the same grounds and over the same prior art?

    The case involved ex parte re-examination of U.S. Patent No. 5,247,434 under Re-examination Control No. 90/007,751.  The technology was related to hemodialysis machines used to treat patients having impaired kidney function.  The patent claimed a hemodialysis apparatus having an interface that controlled several biological parameters:

    26. A hemodialysis machine comprising:
        (a) means for controlling a dialysate parameter selected from a group consisting of dialysate temperature and dialysate concentration, and means for delivering the dialysate to a dialysate compartment of a hemodialyzer; and
        (b) a user/machine interface operably coupled to said dialysate-delivery means, the user/machine interface comprising a touch screen adapted to display an indicium correspond- ing to a parameter pertinent to operation of the hemodialysis machine for performing hemodialysis and to permit the user, by touching the indicium, to cause a change in the parameter.

    Dependent claims recited additional specific features.

    Patent litigation previously ensued between Baxter and a competitor, Fresenius, which filed a declaratory judgment action of invalidity asserting obviousness over several references (including manuals used with prior art hemodialysis machines (the CMS 08 Manual and the Cobe C3 Manual) and a prior art machine (the Seratron System)).  The District Court overruled a jury verdict of obviousness, granting Baxter judgment as a matter of law that Fresenius had not established obviousness by clear and convincing evidence.  In the appeal of that judgment, Fresenius USA, Inc. v. Baxter Int'l, Inc., 582 F.3d 1288, 1299 (Fed. Cir. 2009), the Federal Circuit affirmed, finding that Fresenius had "failed to present any evidence — let alone substantial evidence — that the structure corresponding to the means for delivering dialysate limitation [in claim 26], or an equivalent thereof, existed in the prior art."

    At the same time ("in parallel"), Fresenius had instituted the ex parte re-examination, submitting the same art to the USPTO that it had produced at trial.  The Examiner found claims 26-31 of the '434 patent obvious over the combination of the CMS 08 Manual, the Sarns 9000 Manual, and U.S. Patent No. 4,370,983 (claims 26-29 and 31), or with the addition of U.S. Patent No. 4,710,166 (for claim 30).  The Federal Circuit's earlier decision on the appeal of the District Court decision came down after final rejection by the Examiner but before a decision from the Board, and the Director ordered the Board to consider the Federal Circuit's decision when deciding whether to affirm the Examiner.  The Board did affirm, and with regard to the earlier Federal Circuit decision decided that it was not bound by that decision for two reasons.  First, the standard of review of the Examiner's rejection was whether the claims were obvious by a preponderance of the evidence, as opposed to the clear-and-convincing standard at trial, and second, the claims are given their broadest reasonable meaning before the Patent Office, rather than a meaning limited by the plain meaning, disclosure in the specification, and prosecution history that district courts and the Federal Circuit use when construing claims.  Phillips v. AWH Corp., 415 F.3d 1303, 1315–17 (Fed. Cir. 2005) (en banc).  The Board then affirmed the factual findings and underlying legal conclusion of obviousness.

    Federal Circuit SealThe Federal Circuit majority affirmed, in a decision by Judge Lourie joined by Judge Moore.  The opinion begins by noting the "limited" scope of review available to the Court in view of its implementation of the Supreme Court's decision in Dickinson v. Zurko.  For obviousness, the Court reviews the factual bases for the Board's decision for substantial evidence (which is where "a reasonable mind might accept the evidence to support the finding"), and while the legal conclusion is reviewed de novo, the Court recognized that the factual determinations are often almost if not completely dispositive.  The Court's decision to affirm the Board's obviousness determination was based almost entirely on its finding that the Board's decision was supported by substantial evidence (albeit it also determined that Baxter had waived certain arguments relating to claim 30 and the "means for delivering an anticoagulant").

    Turning to the significance of the District Court's decision and the Federal Circuit's upholding that decision, the majority "rejected" Baxter's arguments relating to the treatment that decision was afforded by the Board.  First, the opinion states that the Board did consider the Court's earlier decision but disagreed with it.  "More fundamentally," however, the majority recognized the differing standards of proof and evidence that attach at trial in contrast to a re-examination proceeding before the Patent Office, and thus the two tribunals can "quite correctly come to different conclusions," quoting In re Swanson, 540 F.3d 1368, 1377 (Fed. Cir. 2008) for the proposition.  The opinion also emphasized that a judicial opinion against an invalidity challenge does not prove a patent valid but on the contrary just establishes (re-establishes, actually) that the patent has not been shown to be invalid.  Accordingly, the majority used this distinction to rationalize its contrary decision regarding obviousness as determined during the reexamination.  Put succinctly:

    This case thus illustrates the distinction between a reexamination and a district court proceeding.  In Fresenius, we upheld the district court's grant of judgment as a matter of law because the patent challenger failed to meet its burden to prove invalidity by clear and convincing evidence — it "failed to present any evidence . . . that the structure corresponding to the means for delivering dialysate limitation [in claim 26], or an equivalent thereof, existed in the prior art" and did not identify "the structure in the specification that corresponds to the means for delivering dialysate" or compare the identified structure to those structures present in the prior art.  Fresenius, 582 F.3d at 1299.  Ultimately, we concluded that the clear and convincing burden of proof in the "means plus function" context "cannot be carried without clearly identifying the corresponding structure in the prior art."  Id. at 1300.

    In contrast, during the reexamination, the examiner sufficiently identified the corresponding structure recited in the '434 patent and identified the structures in the prior art such that a reasonable person might accept that evidence to support a finding that claim 26 is not patentable under a preponderance of the evidence standard of proof.  Moreover, in addition to relying on the CMS 08 Manual, the examiner based those rejections on prior art references that were not squarely at issue during the trial on the invalidity issues, such as Lichtenstein and Thompson.  See Fresenius, 2007 WL 518804, at *7–8 (discussing the Cobe C3 Manual, the CMS 08 Manual, the Sarns 9000, and the Seratron System).  Thus, because the two proceedings necessarily applied different burdens of proof and relied on different records, the PTO did not err in failing to provide the detailed explanation now sought by Baxter as to why the PTO came to a different determination than the court system in the Fresenius litigation.

    The majority also addressed the question of whether it was "erroneously elevating a decision by the PTO over a decision by a federal district court, which decision has been affirmed by this court" by citing some "additional comments."  These include that Congress has established the re-examination procedure to permit these disparate determinations.  Here, the opinion suggests that this may be due in part to assertion of different art that may raise "new issues" based in new prior art, which indeed happened here.  And the opinion concludes with the majority's own determination that the claims are obvious in view of the cited art.

    In her dissent, Judge Newman raises an issue not extensively considered by the majority, what she characterizes as "the agency's nullification of [the Federal Circuit's] final decision" entered previously.  This not only "violates [] the constitutional plan" but "also violates the rules of litigation repose as well as the rules of estoppel and preclusion — for the issue of validity, the evidence, and the parties in interest are the same in this agency reexamination as in the finally resolved litigation."  Continuing, she writes that:

    No authority, no theory, no law or history, permits administrative nullification of a final judicial decision.  No concept of government authorizes an administrative agency to override or disregard the final judgment of a court.  Judicial rulings are not advisory; they are obligatory.

    For these propositions she cites (wisely) to extensive Supreme Court precedent.  From San Remo Hotel, L.P. v. City & County of San Francisco, 545 U.S. 323 (2005):

    The general rule implemented by the full faith and credit statute — that parties should not be permitted to relitigate issues that have been resolved by courts of competent jurisdiction — predates the Republic.  It "has found its way into every system of jurisprudence, not only from its obvious fitness and propriety, but because without it, an end could never be put to litigation."

    From Southern Pacific Railroad v. United States, 168 U.S. 1 (1897):

    This general rule [i.e., the rule of finality of judicial determinations] is demanded by the very object for which civil courts have been established, which is to secure the peace and repose of society by the settlement of matters capable of judicial determination.  Its enforcement is essential to the maintenance of social order; for the aid of judicial tribunals would not be invoked for the vindication of rights of person and property if, as between parties and their privies, conclusiveness did not attend the judgments of such tribunals in respect of all matters properly put in issue, and actually determined by them.

    From Plaut v. Spendthrift Farm, Inc., 514 U.S. 211 (1995):

    The record of history shows that the Framers crafted this charter of the judicial department with an expressed understanding that it gives the Federal Judiciary the power, not merely to rule on cases, but to decide them, subject to review only by superior courts in the Article III hierarchy — with an understanding, in short, that "a judgment conclusively resolves the case" because "a 'Judicial Power' is one to render dispositive judgments."

    (citing 7th Circuit Court Judge Easterbrook, Presidential Review, 40 Case W. Res. L. Rev. 905, 926 (1990)).

    In the face of this precedent, Judge Newman argues that the Court "continues [improperly] to authorize the Patent and Trademark Office to 'revise, overturn, and refuse full faith and credit' to final judgments of the courts, in the words of Chicago & Southern Airlines, 333 U.S. at 114."  This action contravenes the "law of the case" doctrine, which "promotes the finality and efficiency of the judicial process by protecting against the agitation of settled issues," citing Christianson v. Colt Industries, Inc., 486 U.S. 800, 815–16 (1988), a doctrine previously recognized by the Federal Circuit (e.g., in Suel v. Secretary of Health & Human Services, 192 F.3d 981, 984–85 (Fed. Cir. 1999), and Perkin-Elmer Corp. v. Computervision Corp., 732 F.2d 888, 900 (Fed. Cir. 1984)).

    And Judge Newman rejects the distinction recognized by the majority, that different forums may impose different requirements, citing Federated Dep't Stores, Inc. v. Moitie, 452 U.S. 394, 401 (1981) for the rule that "a final judicial determination controls the issue in all forums."  These principles are important for legal repose, she says, wherein "res judicata and collateral estoppel relieve parties of the cost and vexation of multiple lawsuits, conserve judicial resources, and, by preventing inconsistent decisions, encourage reliance on adjudication," quoting Allen v. McCurry, 449 U.S. 90, 94 (1980).  "A patent that has been adjudicated to be valid cannot be invalidated by administrative action, any more than a patent adjudicated to be invalid can be restored to life by administrative action," Judge Newman writes.

    Congressional action in enacting the re-examination statute is not to the contrary, and Congress "did not purport to violate the constitutional strictures governing finality of judicial process," the judge writes, reminding the majority that "[t]he possibilities for vexation and abuse were perceived from the initiation of reexamination" and discounting claims by then Commissioner Diamond in testimony to the House and Senate that "the statute contained various safeguards and 'carefully protects patent owners from reexamination proceedings brought for harassment or spite.'"  Hearings on H.R. 6933, 6934, 3806 & 215, Industrial Innovation & Patent & Copyright Law Amendments, House Comm. on the Judiciary, 96th Cong., 2d Sess. 594 (1980).  These fears have come to fruition, according to her dissent:

    Today, reexamination is part of the tactical armory of litigators.  However, throughout this history, including the current legislative proposals to make reexamination more useful as a less costly alternative to litigation, we have uncovered no suggestion that reexamination is intended to deprive a final judgment of the full faith and credit attendant upon final judgments.  We have found no hint that reexamination of the question of patentability is intended to override judicial resolution of the question of patentability.  Nor would such legislation be contemplated, for "Article III, §1 safeguards the role of the Judicial Branch in our tripartite system by barring congressional attempts 'to transfer jurisdiction [to non-Article III tribunals] for the purpose of emasculating' constitutional courts, and thereby preventing 'the encroachment or aggrandizement of one branch at the expense of the other,'" citing Commodity Futures Trading Comm'n v. Schor, 478 U.S. 833, 850 (1986).

    And in this case Judge Newman finds yet another reason for the Court not to defer to the agency's determination, because the basis for rejection, obviousness, is a matter of law.  In her view, "[e]ven if the Federal Circuit were believed to have erred in its prior decision, the mechanism for correcting an unjust decision is by judicial reopening, not by administrative disregard," citing Christianson at 817.

    Congress clearly intended for re-examination to provide an alternative to costly litigation, not an adjunct, and there is little evidence that Congress contemplated the uses to which re-examination is put today (inter partes as well as ex parte).  Judge Newman's dissent raises separation of powers questions as well as questions of judicial integrity, and unless the Court is inclined to reverse its decision to defer to the USPTO in cases such as this one (either by the panel or en banc), it is likely that the Supreme Court will once again have the occasion to review (and if Judge Newman is right, overrule) how the Federal Circuit has interpreted U.S. patent law.  And in this case, such correction may in fact be necessary.

    In re Baxter International, Inc. (Fed. Cir. 2012)
    Panel: Circuit Judges Newman, Lourie, and Moore
    Opinion for the court by Circuit Judge Lourie; dissenting opinion by Circuit Judge Newman

  • By Donald Zuhn

    IFICA survey on consumer perceptions regarding food technology indicates that many U.S. consumers have favorable opinions concerning the benefits offered by plant and animal biotechnology.  The survey, which was commissioned by the International Food Information Council (IFIC), a nonprofit, nonpartisan organization established in 1985 to effectively communicate science-based information about food safety and nutrition, was conducted by polling 750 U.S. adults between March 7-19, 2012 as to their perceptions on various food technology issues.

    The survey found that 74% of respondents had read or heard at least "a little" about the concept of food biotechnology.  With respect to plant biotechnology in general, respondents who had somewhat or very favorable opinions concerning plant biotechnology (38%) outnumbered those who had somewhat or very unfavorable opinions (20%).  The percent of respondents having somewhat or favorable opinions was up from 32% in 2010.  Almost half (49%) of respondents had favorable opinions concerning the use of biotechnology by farmers to grow more crops in order to help meet food demand.  A majority of respondents noted that they were somewhat or very likely to purchase foods produced through biotechnology in order to provide more healthful fats (71%), avoid saturated fat (68%), or make foods taste better or fresher (69%).  Given the choice between increased pesticide use or biotechnology, 77% of respondents said they would be likely to purchase foods that had been biotechnologically engineered for their ability to reduce pesticide use.  While a majority of respondents said they would be somewhat or very likely to purchase foods produced through biotechnology to achieve a number of specific benefits, the number of respondents saying they would be likely to buy such products had dropped since 2010 (see chart below).

    FIG5
    With respect to animal biotechnology in general, respondents who had somewhat or very favorable opinions concerning animal biotechnology (33%) outnumbered those who had somewhat or very unfavorable opinions (26%).  However, the difference in these groups was less pronounced than it was for biotechnologically engineered plants.  Half of the respondents had a somewhat or very favorable impression regarding the use of genomics to evaluate animals in order to make better breeding decisions to achieve improved meat, milk, and egg quality.  However, only 44% of respondents had a somewhat or very favorable impression regarding the use of genetic engineering to transfer beneficial traits from one animal to another in order to improve nutritional content or lessen environmental impact.  Despite this result, a majority of respondents (71%) still said they would be likely to buy meat, milk, and eggs from animals enhanced through genetic engineering, and a majority of respondents (67%) still said they would be likely to buy fish enhanced through genetic engineering, provided in both cases that the FDA determined that such products were safe (see chart below).

    FIG7
    A majority of respondents (66%) also indicated that they supported the FDA's current food labeling policy for foods produced through biotechnology.  Only 24% of respondents believed additional information should be required on food labels, with only 3% suggesting that the additional information that was needed on labels related to biotechnology.

  • By Donald Zuhn

    USPTO SealThe U.S. Patent and Trademark Office published a notice published in today's Federal Register (77 Fed. Reg. 28541) seeking comments regarding an international effort to revise the standard for Sequence Listing submissions.  The new standard — proposed WIPO ST.26 — would require that Sequence Listings be submitted in extensible mark-up language (XML) format, which the Office indicated would more closely align the requirements of the Sequence Listing standard with those of public sequence database providers.

    Currently, Sequence Listings must be submitted in accordance with World Intellectual Property Organization (WIPO) Standard ST.25 (see portion below), which became effective in 1998.  U.S. Patent Rules concerning application disclosures of certain nucleotide and amino acid sequences (i.e., 37 C.F.R. §§ 1.821 – 1.825) are consistent with WIPO ST.25.

    Sequence Listing
    WIPOIn October 2010, the Committee on WIPO Standards (CWS) established a Task Force, led by the European Patent Organization (EPO), to propose a revised standard for the filing of Sequence Listings in XML format (see Example below).  The XML standard developed by the Task Force, tentatively designated WIPO ST.26, has three components:  (i) the body of the standard, (ii) a first annex setting forth the controlled vocabularies for use with the sequence part of the standard, and (iii) a second annex setting forth the Document Type Definition (DTD) for the standard (the three components making up the new standard can be found at the USPTO's webpage on WIPO ST.26).  The new standard is expected to be adopted by the CWS in 2013.  Meanwhile, the Task Force has begun to explore the development of a tool for converting Sequence Listings from one format into another.

    ST.26 Example
    Noting that standard is likely to be adopted, the Office is requesting comments "on any aspect of the proposed standard or Annexes, transition issues, or expected implementation in the United States."  In particular, the Office's notice lists six topics on which it is seeking public comment: (1) Comprehensiveness and Clarity, (2) Absence of PCT Procedure, (3) Feature Keys and Qualifiers, (4) Definition of a Sequence for which a Sequence Listing is Required, (5) Publications (references), and (6) Transition Issues.  Additional information regarding these topics can be found on pages 28542-53 of the notice.

    Comments regarding the proposed standard can be submitted by e-mail to seq_listing_xml@uspto.gov or by regular mail to:  Mail Stop Comments-Patents, Commissioner for Patents, P.O. Box 1450, Alexandria, VA 22313–1450, marked to the attention of Susan C. Wolski, Office of Patent Cooperation Treaty Legal Administration, Office of the Associate Commissioner for Patent Examination Policy.  Comments must be submitted by July 16, 2012.

  • By Kevin E. Noonan

    RamiprilIn an otherwise unremarkable case of a PTO rejection based on anticipation, Judges Dyk and Lourie engaged in an interesting colloquy on the proper interpretation of what constitutes inherent anticipation, in In re Montgomery.  The case involved claims to methods for "treating or preventing" stroke, using "renin-angiotensin system (RAS)" inhibitors, specifically ramipril.  The claims at issue included the following:

    42.  A method for the treatment or prevention of stroke or its recurrence, wherein said method comprises administering, to a patient diagnosed as in need of such treatment or prevention, an inhibitor of the rennin-angiotensin system, said inhibitor having a ClogP of greater than about 1.

    43.  The method as claimed in claim 42, wherein the inhibitor of the rennin-angiotensin system comprises at least one inhibitor of angiotensin-converting enzyme.

    45.  The method as claimed in claim 43, wherein the inhibitor of angiotensin-converting enzyme comprises ramipril.

    (Emphasis in original)

    The claims were rejected based on any of four prior art references:

    • AIRE (The Acute Infarction Ramipril Efficacy (AIRE) Study Investigators, Effect of Ramipril on Mortality and Morbidity of Survivors of Acute Myocardial Infarction with Clinical Evidence of Heart Failure, 342 Lancet 821 (1993));
    • Frampton (James E. Frampton & David H. Peters, Ramipril: An Updated Review of Its Therapeutic Use in Essential Hypertension and Heart Failure, 49 Drugs 440 (1995) (abstract));
    • HOPE (The HOPE Study Investigators, The HOPE (Heart Outcomes Prevention Evaluation) Study: The Design of a Large, Simple Randomized Trial of an Angiotensin- Converting Enzyme Inhibitor (Ramipril) and Vitamin E in Patients at High Risk of Cardiovascular Events, 12 Can. J. Cardiology 127 (1996)); or
    • Gohlke (Peter Gohlke et al., Angiotensin-Converting Enzyme Inhibition Improves Cardiac Function, 23 Hypertension 411 (1994)) as evidenced by Richer (C. Richer et al., Antihypertensive Drugs in the Stroke-Prone Spontaneously Hypertensive Rat, 19 Clinical & Experimental Hypertension 925 (1997) (abstract), available here.

    The Examiner, and the Board, found that each of these references taught administration of ramipril to individuals at risk for stroke (the Court's opinion noting that the limitation that the RAS inhibitor had "a ClogP of greater than about 1" was inherently a property of ramipril).

    Specifically, the Board made the factual determinations that "[h]ypertension is a known risk for stroke" and that the cited references described studies showing treatment of patients with hypertension with ramipril (although at least in the AIRE study the results were not statistically significant).  The HOPE study was described as involving the combination of ramipril and Vitamin E "in the prevention of myocardial infarction, stroke, or cardiovascular death."  (The HOPE study showed statistically significant reduction in stroke risk, but not until after Montgomery's priority date.)  The Gohlke reference showed "the effects of . . . ramipril on functional and biochemical cardiac parameters in stroke-prone spontaneously hypertensive rats," which found that the treatment "improves cardiac function even at low doses," where Richer established that "[t]he stroke-prone spontaneously hypertensive rat . . . is an experimental model that has been widely used to investigate the potential preventive effects vs stroke and mortality of numerous antihypertensive agents."  The Board construed the claims as having two elements:  "(1) 'to administer an inhibitor of the rennin-angiotensin system,' and (2) 'the patient population receiving the inhibitor . . . encompasses patients diagnosed as required stroke treatment or prevention.'"  The Board held that each reference provided these elements and hence anticipated the claims.

    The Federal Circuit opinion noted that the Board did not rule "directly" on the question of whether the claims contained a requirement that the method be effective at treating or preventing stroke, but said it "appeared to assume that they did include such a requirement."  In rejecting Montgomery's argument that the references did not demonstrate efficacy for using ramipril to treat stroke, the Board found that efficacy was "inherent" and need not be demonstrated, citing In re Cruciferous Sprout Litig., 301 F.3d 1343, 1350 (Fed. Cir. 2002).

    Federal Circuit SealThe Federal Circuit upheld the Board's decision, in an opinion by Judge Dyk joined by Judge Prost; Judge Lourie dissented.  In the majority opinion, Judge Dyk set forth the analytical framework:  first the claims are construed giving claim terms their "broadest reasonable interpretation consistent with the specification," citing In re Bond, 910 F.2d 831, 833 (Fed. Cir. 1990).  Then, the claims are compared to the prior art, and anticipation found if every limitation is contained in a single reference.  In re Aoyama, 656 F.3d 1293, 1296 (Fed. Cir. 2011).  Regarding inherent anticipation, an unrecited limitation is present so long as it is "necessarily present, or inherent, in the single anticipating reference," citing Schering Corp. v. Geneva Pharm., Inc., 339 F.3d 1373, 1377 (Fed. Cir. 2003); but the opinion emphasized the word "necessarily" in this context, finding authority for this proposition in In re Oelrich, 666 F.2d 578, 581 (CCPA 1981).

    The opinion focused on claim 45, with expressly recited ramipril, saying that the other two claims, being broader in scope would also be anticipated.  The Federal Circuit relied on the HOPE reference, finding that its determination that this reference anticipates eliminates any reason to address Montgomery's arguments on the other references.  The HOPE reference satisfied the limitation that ramipril be administered to "a patient diagnosed as in need of [stroke] treatment or prevention" according to the Court, and the opinion states that Montgomery did not dispute this Board finding.

    Turning to the preamble ("for the treatment or prevention of stroke or its recurrence") (which the Board and the Court construed as an affirmative limitation), the opinion noted that while the Board "appeared to assume that the patent included an efficacy requirement," the majority was "skeptical that a proper interpretation of the claims would include an efficacy requirement."  The opinion bases its skepticism on its opinion in Bristol-Myers Squibb Co. v. Ben Venue Laboratories, Inc., 246 F.3d 1368, 1371, 1375 (Fed. Cir. 2001), which it characterized as concerning a "similar "method of treatment" claim; in that case, the Court held that a method "for reducing hematologic toxicity" "merely express[ed] a purpose [] rather than requiring a particular result."  That construction "is even more appropriate here," says the majority, because the Board and the Court applies the "broadest reasonable interpretation" standard.

    After this semantic sojourn, however, the majority finds that its resolution is not necessary, because it agrees with the Board that "even if the claim includes an efficacy requirement, efficacy is inherent in carrying out the claim steps."  "[T]here is no question here that treating stroke-prone patients with ramipril does in fact inevitably treat or prevent stroke," according to the majority, and of course Montgomery does not (and cannot) disagree, since the efficacy of ramipril to treat or prevent stroke is "the entire premise of [Montgomery's] patent."  Relying on Bristol-Myers Squibb, Cruciferous Sprout, and King Pharmaceuticals, Inc. v. Eon Labs, Inc., 616 F.3d 1267, 1270 (Fed. Cir. 2010), the majority held that the HOPE reference disclosed administration of ramipril to "stroke-prone" patients, which "inevitably treats or prevents stroke."  Nor does the law require that ramipril had ever been administered to treat or prevent stroke, provided that the treatment was at least "merely proposed," citing for support the outcome in Schering Corp. v. Geneva Pharm., Inc., 339 F.3d 1373, 1377 (Fed. Cir. 2003), and SmithKline Beecham Corp. v. Apotex Corp., 403 F.3d 1331, 1343-44 (Fed. Cir. 2005).

    Judge Lourie dissented, calling inherency "a very tricky concept in patent law."  Judge Lourie uses Schering Corp. v. Geneva Pharm., Inc. as an example, contrasting the "salutary goal" of the principle in "prevent[ing] subject matter that is effectively in the public's possession from being retrieved by a patent and withdrawn from the public domain" with the risk of "withholding patent protection from that which the public knew nothing about until a later inventor found it."  Sounding like an antipode to Justice Breyer, the dissent states that an "unbounded concept of inherency [] threatens to stymie innovation by withdrawing from the realm of patentability that which has not before been known, used, or benefited from."  This is not Judge Lourie's conception of inherent anticipation, which requires "inevitability," which the Court's cases have been "steadfast" in requiring, citing Bettcher Indus., Inc. v. Bunzl USA, Inc., 661 F.3d 629, 639 (Fed. Cir. 2011); Hansgirg v. Kemmer, 102 F.2d 212, 214 (CCPA 1939); and Glaxo Inc. v. Novopharm Ltd., 52 F.3d 1043, 1047 (Fed. Cir. 1995), the latter case illustrating that "even a very high likelihood" is not enough.

    The alternative, according to Judge Lourie, would be that "a mere proposal for further experimentation could anticipate a claimed invention"; "[a]n invitation to investigate is not an inherent disclosure."  Metabolite Labs., Inc. v. Lab. Corp. of Am. Holdings, 370 F.3d 1354, 1367 (Fed. Cir. 2004).  "[I]nnovation should not be impeded by mere speculation."  Turning to the majority's interpretation of the HOPE reference, Judge Lourie states that "[a] description of a process, even if not carried out, is an anticipation of that process.  But a mere description of a process that, if it had been carried out, might yield a particular undisclosed result is not an inherent anticipation of that result"; Judge Lourie considers the HOPE reference to be better characterized as the latter of these two situations and thus not to anticipate the claims.

    While perhaps not invoking the establishment of a trend, the dissent does make a case that the current members of the Court have become more likely to find inherent anticipation under a broader set of circumstances than have been applied heretofore.  Whether this is another example of the turn of this Court, under persistent influence by the Supreme Court, to be less "patent friendly" than it was previously (at least as some have perceived) will depend on whether and to what extent this trend continues.

    In re Montgomery (Fed. Cir. 2012)
    Panel:  Ciercuit Judges Lourie, Dyk, and Prost
    Opinion for the court by Circuit Judge Dyk; dissenting opinion by Circuit Judge Lourie

  • By Sherri Oslick

    Gavel About Court Report:  Each week we will report briefly on recently filed biotech and pharma cases.

    Esoterix Genetic Laboratories, LLC v. Life Technologies Corp. et al.
    1:12-cv-00411; filed April 26, 2012 in the Middle District of North Carolina

    • Plaintiff:  Esoterix Genetic Laboratories, LLC
    • Defendants:  Life Technologies Corp.; Applied Biosystems, LLC; Ion Torrent Systems, Inc.

    Infringement of U.S. Patent Nos. 5,670,325 ("Method for the Detection of Clonal Populations of Transformed Cells in a Genomically Heterogeneous Cellular Sample," issued September 23, 1997), 5,882,856 ("Universal Primer Sequence for Multiplex DNA Amplification," issued on March 16, 1999), and 6,207,372 (same title, issued March 27, 2001) based on defendants' manufacture and sale of products, kits, and devices used in methods for detecting certain cells, cancer, lesions, or changes in a biological sample or tissue and in the detection and amplification of DNA sequences and related products.  View the complaint here.


    Bayer Pharma AG et al. v. Watson Pharmaceuticals Inc. et al.

    1:12-cv-00517; filed April 25, 2012 in the District Court of Delaware

    • Plaintiffs:  Bayer Pharma AG; Bayer Intellectual Property GmbH; Bayer HealthCare Pharmaceuticals Inc.
    • Defendants:  Watson Pharmaceuticals Inc.; Watson Laboratories Inc.; Watson Pharma Inc.

    Infringement of U.S. Patent Nos. 6,362,178 ("2-phenyl Substituted Imidazotriazinones as Phosphodiesterase Inhibitors," issued March 26, 2002) and 7,696,206 (same title, issued April 13, 2010) following a Paragraph IV certification as part of Watson's filing of an ANDA to manufacture a generic version of plaintiffs' Staxyn® (vardenafil hydrochloride, used to treat erectile dysfunction).  View the complaint here.


    Abbott Laboratories et al. v. Agila Specialties Private Ltd. et al.

    1:12-cv-00520; filed April 25, 2012 in the District Court of Delaware

    • Plaintiffs:  Abbott Laboratories; Wisconsin Alumni Research Foundation
    • Defendants:  Agila Specialties Private Ltd.; Strides Arcolab Ltd.; Strides Inc.

    Infringement of U.S. Patent Nos. 6,136,799 ("Cosolvent Formulations," issued October 24, 2000), 6,361,758 (same title, issued March 26, 2002), and 5,597,815 ("Prevention of Hyperphosphatemia in Kidney Disorder Patients," issued January 28, 1997) following a Paragraph IV certification as part of Agila's filing of an ANDA to manufacture a generic version of Abbott's Zemplar® (paricalcitol, used to treat secondary hyperparathyroidism in patients with kidney failure).  View the complaint here.


    Precision BioSciences, Inc. v. Cellectis SA et al.

    5:12-cv-00219; filed April 24, 2012 in the Eastern District of North Carolina

    • Plaintiff:  Precision BioSciences, Inc.
    • Defendants:  Cellectis SA; Cellectis bioresearch; Cellectis bioresearch Inc.

    Infringement of U.S. Patent No. 8,163,514 ("Methods of Cleaving DNA with Rationally-Designed Meganucleases," issued April 24, 2012) based on Cellectis' manufacture, use, and sale of meganucleases targeting the GS gene in Chinese Hamster Ovary cells, meganucleases targeting the HPRT gene in Chinese Hamster Ovary cells, and menganucleases targeting the HIV1 genome.  View the complaint here.


    OSI Pharmaceuticals, LLC et al. v. Roxane Laboratories, Inc.

    2:12-cv-02384; filed April 20, 2012 in the District Court of New Jersey

    • Plaintiffs:  OSI Pharmaceuticals, LLC; Pfizer, Inc.; Genentech, Inc.
    • Defendant:  Roxane Laboratories, Inc.

    Infringement of U.S. Patent Nos. RE41,065 ("Alkynyl and Azido-Substituted 4-Anilinoquinazoline," issued May 5, 1998), 6,900,221 ("Stable Polymorph on N-(3-Ethynylpheny1)-6, 7-Bis(2MethoxyEthoxy)-4-Quinazolinamine Hydrochloride, Methods of Production, and Pharmaceutical Uses Thereof," issued May 31, 2005), and 7,087,613 ("Treating Abnormal Cell Growth With A Stable Polymorph on N-(3-Ethynylpheny1)-6,7-Bis(2MethoxyEthoxy)-4-Quinazolinamine Hydrochloride," issued August 8, 2006) following a Paragraph IV certification as part of Roxane's filing of an ANDA to manufacture a generic version of OSI's Tarceva® (erlotinib, used to treat non-small cell lung cancer and advanced pancreatic cancer).  View the complaint here.

  • Calendar

    May 15, 2012 – FDA's New Biosimilar Guidances (Law Seminars International) – 3:00 – 4:00 pm (Eastern)

    May 16, 2012 – Patent-Eligible Subject Matter after Mayo v. Prometheus: Exploring the Path Forward (George Washington University Law School and Biotechnology Industry Organization) – Washington, DC

    May 16-18, 2012 – Fundamentals of Patent Prosecution 2012: A Boot Camp for Claim Drafting & Amendment Writing (Practising Law Institute) – Chicago, IL

    May 21, 2012 – Patent Institutions Summit (Stanford Program in Law, Science & Technology and the Berkeley Center for Law & Technology) – Stanford Law School

    May 22-23, 2012 – Biosimilars*** (American Conference Institute) – New York, NY

    June 5, 2012 – Orange Book Use Codes: Impact of Caraco v. Novo Nordisk (Strafford) – 1:00 – 2:30 pm (EDT)

    June 6, 2012 – Biotechnology/chemical/ pharmaceutical (BCP) customer partnership meeting (U.S. Patent and Trademark Office) – 9:00 am – 4:30 pm (ET)

    June 8-12, 2012 – 2012 MidYear Meeting (Association of American Law Schools) – Berkeley, CA

    June 13-15, 2012 – Fundamentals of Patent Prosecution 2012: A Boot Camp for Claim Drafting & Amendment Writing (Practising Law Institute) – New York, NY

    June 18-21, 2012 – BIO International Convention (Biotechnology Industry Organization) – Boston, MA

    June 20-21, 2012 – International Forum on Pharma Patent Lifecycles*** (C5) – London, England

    June 24-26, 2012 – IP Business Congress (Intellectual Asset Management (IAM) magazine) – Cascais, Portugal

    June 25-26, 2012 – Hatch-Waxman Boot Camp*** (American Conference Institute) – San Diego, CA

    July 11-13, 2012 – Fundamentals of Patent Prosecution 2012: A Boot Camp for Claim Drafting & Amendment Writing (Practising Law Institute) – San Francisco, CA

    July 30 to August 1, 2012 – Intensive Patent Law Seminar (Chisum Patent Academy) – Seattle, WA

    ***Patent Docs is a media partner of this conference or CLE

  • The Chisum Patent Academy will be offering its next Intensive Patent Law Seminar from July 30 to August 1, 2012 in Seattle, WA.  The three-day seminar will focus on recent and important legislative and case law developments in U.S. patent law, including the American Invents Act of 2011, patent-eligible subject matter in the wake of Mayo v. Prometheus, post-KSR nonobviousness decisions, Therasense and the future of inequitable conduct, and the Federal Circuit's ongoing schism over patent claim construction.

    The seminar is co-taught by Donald Chisum, author of the treatise Chisum on Patents (LexisNexis), and Janice Mueller, who was a tenured full Professor at the University of Pittsburgh School of Law from 2004-2011.  The registration fee for the seminar is $2,000; a maximum of ten registrations will be accepted for the seminar.  Those interested in registering for the seminar can do so here.  Additional information regarding the seminar can be obtained here or by e-mailing info@chisum.com.

    Chisum Patent Academy

  • George Washington University Law SchoolThe George Washington University Law School and Biotechnology Industry Organization (BIO) will be holding a public roundtable entitled "Patent-Eligible Subject Matter after Mayo v. Prometheus: Exploring the Path Forward" from 2:00 – 5:00 pm on May 16, 2012 at The George Washington University Law School, 716 20th Street NW, Washington, DC.  Additional information about the roundtable, including a list of participants, can be Biotechnology Industry Organization (BIO)found here.  A reception will take place following the roundtable.

    There is no registration fee for the roundtable, but those interested in attending must RSVP by sending an e-mail to iplaw@law.gwu.edu with "Bio" in the subject line.

  • LSI - Law Seminars International - blueLaw Seminars International (LSI) will be offering a one-hour telebriefing on the "FDA's New Biosimilar Guidances" on May 15, 2012 from 3:00 – 4:00 pm (Eastern).  Timothy J. Shea, Jr. of Sterne Kessler will moderate a panel including Jennifer L. Fox of Brinks Hofer Gilson & Lione and Dr. Denise M. Kettelberger of Faegre Baker Daniels.  The panel will discuss the practical and legal implications of the proposed guidance documents issued by the FDA in February, and will consider strategies for companies seeking to market biosimilar products and for brand companies seeking to maintain market share in the face of biosimilar competition.  Among the topics to be covered are:

    • The scope and applicability of the proposed guidelines: What they do and do not cover;
    • The FDA's stepwise approach to demonstrating biosimilarity;
    • Which scientific considerations the FDA considers most important in evaluating biosimilarity;
    • The extent and nature of clinical trials that will likely be required for approval;
    • How changes in structure, formulation and manufacturing process will impact the review process; and
    The interplay between the approval process and patent strategies.

    A Q&A will follow the presentation and last for up to 30 minutes.

    The registration fee is $125 per caller and $50 each additional person on the same line who desires continuing education credit.  Those interested in registering for the telebriefing, can do so here.