•     By Sherri Oslick

    Glaxosmithkline_gsk
    Patent Docs
    readers anxiously awaiting GSK/Tafas’ brief will have to wait a little longer.  On August 14, the parties jointly moved to modify the briefing schedule; the motion was granted today (September 2).  The schedule as it now stands is as follows:

    • September 24, 2008:  Appellees’ briefs due

    • October 15, 2008:  Appellants’ reply brief and joint appendix due

    By an additional joint motion, also granted today, oral arguments will be scheduled on the December 2008 argument calendar.

    For additional information regarding the appeal, please see:

    • "Public Interest Groups Back USPTO in Tafas v. Dudas Appeal," August 5, 2008
    • "USPTO Files Opening Brief in Tafas v. Dudas Appeal," July 22, 2008
    • "Save the Date — Initial Scheduling of the Tafas/GSK v. Dudas Appeal," May 21, 2008
    • "USPTO to Appeal Tafas/GSK v. Dudas," May 7, 2008

  •     By Kevin E. Noonan

    Monsanto
    Monsanto has been very successful in defending its Roundup Ready® franchise of genetically-engineered crop varieties.  Monsanto sells patented seeds to a variety of crop plants, including soybeans, that are resistant to Monsanto’s Roundup® glyphosphate herbicide.  These sales are conditioned by an agreement, termed the "Technology Agreement" that requires purchasers to pay a one-time license fee, and agreeing not to plant themselves, or supply to others, "saved" seeds, i.e., seeds produced from the originally purchased seeds.  Just like with the hybrid seeds sold during the "green revolution" a generation ago, this system ensured that farmers purchase and license Roundup Ready® soybean seeds each planting season.  Over the past 10 years, Monsanto has filed suit 125 times against individual farmers it accused of infringing its patents, including U.S. Patent Nos. 5,352,605 and No. 5,633,435 (RE39,247), that protect recombinant seed resistant to glyphosphate herbicide.  Only eight of these lawsuits have gone to trial, while in the remainder, the accused infringer agreed to settlements that generally included an admission of liability.

    Roundup_ready_soybeans
    Monsanto announced today the latest of these settlements, in a lawsuit against the farmer’s co-operative Pilot Grove Cooperative Elevator, Inc. (PGCE).  This lawsuit was different from the others:  instead of suing individual farmers, Monsanto sued the Elevator corporation, a farmers’ co-op, for aiding infringement by more than 100 Missouri farmers.  In the settlement, PGCE acknowledged infringement and agreed to purchase $1.1 million in Monsanto seed products over the next six years.  The co-operative also agreed to spend $275,000 to fund college scholarships for local members of the Future Farmers of America and 4H Clubs.  Finally, the co-operative agreed to provide training to its employees and a stewardship program to avoid future infringement, as well as funding a third party organization to provide training for non-infringement.

    Monsanto spokesman, Scott Baucum, Director of U.S. Commercial Trait Stewardship, said in a press release that:

    We pursue these cases for a number of important reasons.  First, we owe it to the hundreds of thousands of Monsanto farmer customers who are abiding by their contracts to assure a level playing field, and that some farmers don’t have an unfair advantage.  Also, while it’s important to Monsanto to protect our investment, it is extremely important to the entire agricultural community that we are able to continue to reinvest in new and better seed technology.  For every $10 a farmer spends on seed, Monsanto invests $1 in research and development.

    Monsanto also endeavored to minimize any perception that it was Goliath to American farmer Davids.  The company said in its press release that it is "relatively rare" that it sues farmers for saving seed, amounting to only a small fraction of its 250,000 customers/year of its soybean product.  Separately, Monsanto spokeswoman Janice Person said that the farmers’ activities in saving recombinant seed for planting in subsequent years was akin to rental agreements for videos and DVDs, where the renter agrees not to copy movies for sale to third parties.

    Monsanto has been awarded $21.6 million in its victorious lawsuits, and The Center for Food Safety estimates that Monsanto has received between $85 million and $160 million in settlements, which remain confidential.  Monsanto has said that it has donated these monies to charity.

    Despite all its successes, recent Supreme Court decisions, particularly Quanta Computer, Inc. v. LG Electronics, Inc., may indicate an Achilles’ heel to the company’s patenting strategy (see "Quanta Computer, Inc. v. LG Electronics, Inc. (2008)").  Settlements thus provide an ideal way for Monsanto to continue to protect its business without subjecting its patents, or patenting activities, to further court scrutiny.  Settlements are also a way to reduce the amount of negative publicity (although probably doing little to assuage farmers’ resentments) over enforcing its patents; this is particularly true in light of the almost universal admission of infringement liability in these settlements, like the one announced today.

    For additional information regarding other related topics, please see:

    • "Monsanto Co. v. David (Fed. Cir. 2008)," February 6, 2008
    • "Court Report," February 3, 2008
    • "Court Report," January 28, 2008
    • "Court Report," January 13, 2008
    • "Court Report," January 7, 2008
    • "Supreme Court Fails to Grant Certiorari in Monsanto Co. v. McFarling," January 7, 2008
    • "Court Report," December 16, 2007
    • "Court Report," November 18, 2007
    • "Court Report," October 21, 2007
    • "Court Report," July 1, 2007
    • "Monsanto Co. v. McFarling (Fed. Cir. 2007)," June 4, 2007
    • "Court Report," May 20, 2007
    • "Court Report," May 7, 2007
    • "Court Report," April 15, 2007
    • "Court Report," March 11, 2007
    • "Court Report," March 4, 2007
    • "Court Report," February 28, 2007

  •     By Donald Zuhn

    Uspto_seal_no_background_2
    In an e-Commerce e-Alert distributed on Friday, the U.S. Patent and Trademark Office announced that it was seeking up to 1,000 registered practitioners to help with a pilot test of the Office’s new online Continuing Education for Practitioners (CEP) system.  According to the Office’s call for volunteers, the goal of the CEP system is "to increase efficiency, reduce pendency, and improve quality in the patent process."

    The CEP system would achieve this goal by presenting "brief educational materials" concerning, for example, recent USPTO rule changes or revised patent examination guidelines, and then prompting practitioners to respond to "one or more verification questions."  Because practitioners would have ready access to the educational materials while responding to the verification questions, the purpose of the questions would be to verify that the practitioner reviewed the educational materials, rather than to test the practitioner’s knowledge or skills.

    Under the CEP system, practitioners would be required to complete one CEP program per year, wherein a program consists of reviewing the education materials and responding to the verification questions.  According to the Patent Office, each program will require about one hour to complete.

    To ensure compliance, the CEP system would automatically notify practitioners of the training requirements, send appropriate reminder notices, and track completion of CEP programs.  For practitioners who timely comply with the CEP requirements, no fees will be assessed; fees will be assessed, however, for failure to timely comply with the requirements.

    Pilot participants will only be required to complete one program (although additional programs will be available for review).  In addition, the Office stated that participation in the pilot will count towards a participant’s first year CEP requirement "at such time as the USPTO makes CEP a requirement."  Registered practitioners interested in participating in the CEP pilot should send an e-mail, including your name, registration number, telephone number, and e-mail address, to OEDonline@uspto.gov, or call Bill Griffin of the Office of Enrollment and Discipline at 571-272-4097.

  •     By Sherri Oslick

    Gavel_4
    About
    Court Report:  Each week we will report briefly on recently filed
    biotech and pharma cases, and a few interesting cases will be selected
    for periodic monitoring.


    Sanofi-Aventis et al. v. Apotex, Inc. et al.

    3:08-cv-04320; filed August 27, 2008 in the District Court of Delaware

    Infringement of U.S. Patent No. 5,338,874 ("Cis oxalato (trans 1-1,2-cyclohexanediamine) PT(II) Having Optically High Purity," issued August 16, 1994) following a Paragraph IV certification as part of Apotex’s filing of an ANDA to manufacture a generic version of plaintiffs’ Eloxatin® (oxaliplatin for injection, used to treat colorectal cancer).  View the complaint here.


    Endo Pharmaceuticals Inc. et al. v. Sandoz Inc.

    1:08-cv-00534; filed August 22, 2008

    Infringement of U.S. Patent No. 5,958,456 ("Controlled Release Formulation (Albuterol)," issued September 28, 1999) following a Paragraph IV certification as part of Sandoz’s filing of an ANDA to manufacture a generic version of Endo’s Opana® ER (oxymorphone hydrochloride, used to treat moderate to severe pain in patients requiring continuous, around-the-clock opioid treatment for an extended period of time).  View the complaint here.


    CIMA Labs Inc. et al. v. Barr Laboratories Inc. et al.

    1:08-cv-00531; filed August 21, 2008 in the District Court of Delaware

    Infringement of U.S. Patent Nos. 6,024,981 ("Rapidly Dissolving Robust Damage Form," issued February 15, 2000) and 6,221,392 (same title, issued April 24, 2001), licensed to Azur Pharma, following a Paragraph IV certification as part of Barr’s filing of an ANDA to manufacture a generic version of Azur’s FazaClo® (clozapine, used to treat schizophrenia).  View the compliant here.

  • Calendar_3
    September 11, 2008 – Developments in Pharmaceutical and Biotech Patent Law (Practising Law Institute) – New York, NY

    September 11-12, 2008 – Current Issues in Complex IP Licensing (Law Seminars International) – Philadelphia, PA

    September 15-16, 2008 – Biotech Patents*** (American Conference Institute)

    September 21-23, 2008 – 2008 Annual Meeting (Intellectual Property Owners Association) – San Diego, CA

    September 22-23, 2008 – USPTO Boot Camp: Patent Edition*** (American Conference Institute) – Alexandria, VA

    September 22-23, 2008 – FDA Boot Camp*** (American Conference Institute)

    September 22-23, 2008 – Patent Litigation 2008 (Practising Law Institute) – San Francisco, CA

    September 22-23, 2008 – 2008 World Stem Cell Summit (Genetics Policy Institute) – Madison, WI

    September 23-24, 2008 – Biotech Patenting (C5) – London, England

    October 6-7, 2008 – Patent Litigation 2008 (Practising Law Institute) – McLean, VA

    October 7-8, 2008 – Global Patent Litigation*** (American Conference Institute) – New York, NY

    October 15, 2008 – Developments in Pharmaceutical and Biotech Patent Law (Practising Law Institute) – San Francisco, CA

    October 15-16, 2008 – Pharmaceutical Congress on Paragraph IV Disputes*** (Center for Business Intelligence) – Philadelphia, PA

    October 15-16, 2008 – Advanced Courses (Patent Resources Group) – Santa Ana Pueblo, NM

    October 15-17, 2008 – Maximizing Pharmaceutical Patent Lifecycles*** (American Conference Institute) – New York, NY

    October 23-24, 2008 – Patent Litigation 2008 (Practising Law Institute) – Chicago, IL

    October 28-29, 2008 – Pharma/Biotech IP Due Diligence*** (C5) – Amsterdam, Netherlands

    November 10-11, 2008 – Patent Litigation 2008 (Practising Law Institute) – Atlanta, GA

    November 12-14, 2008 – Structuring, Negotiating and Managing Pharma/Biotech Collaborative Agreements (American Conference Institute) – New York, NY

    November 17-18, 2008 – Patent Litigation 2008 (Practising Law Institute) – New York, NY

    November 19-20, 2008 – Paragraph IV on Trial*** (American Conference Institute) – New York, NY

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

  •     By Kevin E. Noonan

    Administrative_office_of_the_us_cou
    The annual report from the Director of the Administrative Office of the U.S. Courts, James C. Duff, was released last week.  Entitled "Judicial Business of the United States Courts," this document (weighing in at 416 pages and containing hundreds of pages of tabulated information) contained a few interesting items of information for anyone trying to assess whether the patent system is "broken" in the federal courts.

    Federal_circuit_seal_2
    Appeals at the Federal Circuit are down 13%, a figure consistent with the decrease in appellate filings in the regional circuit courts of appeal (-12.3%).  In fact, filings for 2007 were at about the same level as in 2003.  This decrease is not due to patent filings, however, but rather to other areas of the Court’s jurisdiction (like the Merit Systems Protection Board and Court of Appeals for Veterans Claims).  In the twelve month period ending September 30, 2007, the Court heard a total of 73 appeals, deciding 34 after oral hearing and 38 on the briefs.  The report also compared the Court’s review of district court and BPAI decisions between 2006 and 2007:

    Table_1_2

    Two thirds of CAFC appeals were decided within five months in 2007, and 100% of appeals decisions rendered within eight months of filing.

    Us_district_court_2
    In the district courts there was an overall decrease in civil lawsuit filings of 0.8%.  Federal question jurisdiction cases rose by 3.4%, and cases with U.S. as plaintiff or defendant rose by 5.8%; diversity of citizenship cases fell by 9.6% (this mostly due to consolidation of personal injury lawsuits involving asbestos and diet drugs in the Eastern District of Pennsylvania).  In the district courts during this period, the following statistics for patent cases were reported:

    Table_2

    Since 2003, all intellectual property lawsuits increased by 1,848 (which pales in comparison to the increase of 16,305 personal injury cases during the same period).  The report provides a historical comparison on the number of patent lawsuits commenced in each year since 2003:

    Table_3

    Using the same statistics, the report shows the judicial districts having the most patent activity in 2007:

    Table_4

    During the period, there were 2,762 pending patent lawsuits, of which 1,945 showed no court action during the reporting period.  Of the remaining cases, there were 409 actions after pretrial activities were complete, 31 bench trial verdicts, and 63 jury trial verdicts.  3.4% of all patent cases went to trial, compared with 1.7% of trademark cases, 1.0% of copyright cases, 46.7% of personal injury cases, and an overall rate of 4.1% of all civil litigation.  Interestingly, there were no patent cases reported in the 27 civil cases that took more than 20 trial days (the majority of civil cases, 1,227 of 3,387 total cases, took between four and nine trial days).

    Finally, the number of patent cases pending more than three years increased, from 353 in 2006 to 408 in 2007; during the same period, trademark (113 in 2006, 121 in 207) and copyright (107 cases in each year) showed a substantially unchanged number of cases having greater than a three-year pendency.

    Easter_district_of_texas_seal
    The report confirms some generally-held opinions, such as the high number of patent cases brought in the Eastern District of Texas, but there are some results that run contrary to the prevailing wisdom.  Although Texas’ Eastern District tops the list of pending patent dockets, there are significant numbers of suits pending in other jurisdictions.  The number of patent cases, at either the district court or appellate levels, is not exploding, nor has the case load of the Federal Circuit shown any dramatic increase; indeed, the number of cases considered by the Court has actually gone down.  It is also somewhat surprising that the reversal rate for decisions of the district court is as low as 17%, after there being years where the rate was in excess of 40%, and that the reversal rate of the BPAI is identically low.  The latter statistic may reflect the reality that the Federal Circuit appeals route under 35 U.S.C. § 141 is infrequently taken, or that the Board decides not to budge over issues that it believes it has sound arguments that will prevail on appeal.

    The complete report can be downloaded here.

  • 2008_world_stem_cell_summit
    The Genetics Policy Institute will be holding the 2008 World Stem Cell Summit on September 22-23 in Madison, WI.  The Summit, which is being hosted by the University of Wisconsin Stem Cell & Regenerative Medicine Center and WiCell Research Institute, will bring together researchers, clinicians, business pathfinders, key policy-makers, regulators, advocates, and experts in law and ethics to give presentations, share information, and chart the future of regenerative medicine.  Among the presentations to be offered at the Summit will be:

    • Reprogramming — A New Vision for Creating Patient Specific Cells:  Keynote Presentation by Dr. James Thomson of the University of Wisconsin-Madison
    • Stem Cell Law:  The Ultimate Road Map to Getting to "Go"
    • The History and Future of Stem Cells — Legal, Regulatory and Ethical Issues:  Keynote Presentation by Alta Charo of the University of Wisconsin-Madison
    • Panel Discussion:  Legal, Regulatory and Ethical Issues

    A complete agenda for the Summit can be found here, and an overview of the Summit’s presentations and panel discussions can be found here.

    In addition, the Summit will offer a series of table discussions by stem cell experts in the areas of ethics, law, science, business, politics, patient advocacy, philanthropy, and medicine.  Among the table discussions to be offered will be:

    • Weeding the Patent Thicket
    • Constitutional Battles Ahead
    • The Law Firm and Client’s Essential Guide to Stem Cell Law

    A complete list of table discussions can be found here.

    The registration fee ranges from $250 (for students) to $495 (for academic, government and non-profit attendees) or $995 (for industry & for-profit corporate attendees).  The registration fee for industry and for-profit corporate attendees after September 8, 2008 is $1,495.  Those interested in registering for the conference can do so here.

    Patent Docs is a media partner of the 2008 World Stem Cell Summit.

  •     By Christopher P. Singer

    Uspto_seal_background
    In an August 27, 2008 notice, the U.S. Patent and Trademark Office (USPTO) announced that it is changing certain forms to remove language that requests a duplicate copy of the form be submitted for fee processing purposes.  Previously, the duplicate copy of forms that contained an authorization to charge fees to a deposit account allowed for faster processing, because hardcopy paper application files were maintained in one area of the Office, while fee processing was done in another area of the Office.  Currently, with the push to go paperless, the Office scans all incoming submissions into the Image File Wrapper (IFW) of an application, a reexamination proceeding, or a patent, including forms that contain an authorization to charge or credit a fee amount to a deposit account.  Because the form is scanned into IFW, it is available and viewable throughout the PTO for all purposes, including fee processing.  The Office is working on revising a number of forms in order to remove the "duplicate copy" language.  Going forward, even if a duplicate copy of a certain form is needed (if it is not scanned or under a secrecy order), the USPTO will make the required copy for fee processing purposes.

  •     By Donald Zuhn

    Aba
    On Monday, the American Bar Association (ABA) Standing Committee on Ethics and Professional Responsibility released a statement regarding a new ethics opinion (Formal Opinion 08-451), which concludes that U.S. lawyers can outsource legal and nonlegal work provided that they adhere to ethics rules regarding competence, supervision, protection of confidential information, reasonable fees, and not assisting in the unauthorized practice of law.  The opinion, entitled "Lawyer’s Obligations When Outsourcing Legal and Nonlegal Support Services," outlines the ethics obligations of lawyers and firms that wish to utilize legal and nonlegal outsourcing.

    Stating that "[a] lawyer may outsource legal or nonlegal support services provided the lawyer remains ultimately responsible for rendering competent legal services to the client," the opinion notes that lawyers and law firms engage lawyers and nonlawyers for various legal and nonlegal support services, ranging from "the use of a local photocopy shop for the reproduction of documents, to the retention of a document management company for the creation and maintenance of a database for complex litigation, . . . or even to the engagement of a group of foreign lawyers to draft patent applications."  The opinion acknowledges, however, that "[t]he challenge for an outsourcing lawyer is . . . to ensure that tasks are delegated to individuals who are competent to perform them, and then to oversee the execution of the project adequately and appropriately."

    Uspto_seal_no_background_2_2
    Notwithstanding the ABA opinion — and its reference to the outsourcing of patent application drafting to foreign lawyers — the U.S. Patent and Trademark Office recently reminded patent practitioners that the export of subject matter abroad pursuant to a USPTO-issue foreign filing license is limited to purposes related to the filing of foreign patent applications, and that the foreign filing license does not authorize exporting of subject matter abroad for the preparation of patent applications to be filed in the United States (see "PTO Issues Notice on Scope of Foreign Filing Licenses").  As the USPTO noted, U.S. patent practitioners wishing to outsource patent application drafting to foreign lawyers are not without recourse, as these practitioners can contact the Bureau of Industry and Security (BIS) at the Commerce Department in order to secure the appropriate clearances.

    Thus, while the new ABA ethics opinion permits U.S. lawyers to outsource legal support services to foreign lawyers, patent practitioners would be wise to, at a minimum, refrain from outsourcing the drafting of patent applications to foreign lawyers.  Patent practitioners who intend to outsource other types of legal support tasks (e.g., document review) are advised to consult the ABA opinion before doing so.

  •     By Kevin E. Noonan

    We may have reached the high-water mark on the expansion of the inequitable conduct doctrine.  Recent decisions from the Federal Circuit seem to signal a retrenchment in the Court’s treatment of the doctrine, and its willingness to affirm district court judgments finding inequitable conduct, particularly in the context of summary judgment decisions.  One of the first indications of this new direction came in the Eisai Co. v. Dr. Reddy’s Laboratories, Inc. decision last month, where Judge Rader forcefully reminded us that finding inequitable conduct should be "a high bar," citing the Court’s en banc decision in Kingsdown Medical Consultants, Ltd. v. Hollister Inc., 863 F.2d 867, 876 (Fed. Cir. 1988).  In doing so, the Court cast some doubt on the wisdom of recent decisions that expanded the inequitable conduct doctrine to encompass improperly claiming small entity status (Nilssen v. Osram Sylvania, Inc.), improperly filing a petition to make special (General Electro Music Corp. v. Samick Music Corp.), failing to disclose that a declarant had been a paid consultant prior to filing an expert declaration under 37 C.F.R. § 1.132 (Ferring B.V. v. Barr Laboratories, Inc.), misjoinder of inventorship (PerSeptive Biosystems, Inc. v. Pharmacia Biotech, Inc.), and inaccuracies in an expert declaration (Aventis Pharma S.A. v. Amphastar Judge_rader_3
    Pharma, Inc.
    ).  Indeed, the beginnings of the trend may have started with Judge Rader’s spirited dissent in Aventis Pharma.  A determination of inequitable conduct, according to Judge Rader (at right) in the Eisai decision, should include evidence of affirmative instances of "culpable conduct" rather that mere omissions, citing the greater evidentiary difficulties that should attach when intent must be discerned from negligent conduct.  His opinion also emphasized that a defendant must establish intent by clear and convincing evidence.

    Federal_circuit_seal_2
    This trend continues today in the Federal Circuit’s decision reversing summary judgment of inequitable conduct against the patentee in Star Scientific, Inc. v. R.J. Reynolds Tobacco Co.  The patents-in-suit, U.S. Patent Nos. 6,202,649 and 6,425,401 (filed as a continuation of the ‘649 patent), were directed to methods for curing tobacco in a way that reduced the amount of a carcinogen, tobacco-specific nitrosamines (TSNAs), in the cured product used in cigarettes and other tobacco-containing products.  The undisclosed information was a letter from one of Star Scientific’s consultants, Dr. Harold Burton, relating to curing methods used in China that resulted in low levels of TSNAs.  The attorney who prosecuted the ‘649 patent was aware of this letter, but "ultimately concluded that neither [the letter itself] nor its content was material to the contemplated patent application," after speaking with Dr. Burton.  Also undisclosed was experimental data generated by Dr. Burton relating to reduced TSNA levels in cured tobacco.

    Star_scientific
    During prosecution of these patents, Star Scientific transferred responsibility from its first set of prosecuting attorneys at Sughrue, Mion, Zin, Macpeak & Seas to a second set at Banner and Witcoff.  The Banner attorneys also became aware of the Burton letter, from litigation counsel (Crowell & Moring) in Star Scientific’s patent litigation in the District Court against R.J. Reynolds; litigation counsel opined that this information should be disclosed to the U.S. Patent and Trademark Office during prosecution of the ‘401 patent.  The Banner attorneys considered the Burton letter, and the experimental data, decided neither was material and did not need to be disclosed, and neither was disclosed during prosecution of the ‘401 patent.  The file transfer formed the basis for R.J. Reynolds’ inequitable conduct theory, which posited that Star Scientific did not want the Banner attorneys to be aware of the Burton letter or experimental data so it could be concealed from the Patent Office during prosecution of the ‘401 patent.  The District Court agreed and granted summary judgment in favor of R.J. Reynolds that neither patent was enforceable due to inequitable conduct.

    The Federal Circuit disagreed, in a unanimous decision by Chief Judge Michel joined by Judges Schall and Dyk.  The Court began its analysis by setting up the analytical framework:

    To successfully prove inequitable conduct, the accused infringer must present "evidence that the applicant (1) made an affirmative misrepresentation of material fact, failed to disclose material information, or submitted false material information, and (2) intended to deceive the [PTO]."  Further, at least a threshold level of each element — i.e., both materiality and intent to deceive — must be proven by clear and convincing evidence.  And even if this elevated evidentiary burden is met as to both elements, the district court must still balance the equities to determine whether the applicant’s conduct before the PTO was egregious enough to warrant holding the entire patent unenforceable.  Thus, even if a threshold level of both materiality and intent to deceive are proven by clear and convincing evidence, the court may still decline to render the patent unenforceable [citations omitted].

    The CAFC goes on to say that the "need to strictly enforce the burden of proof and elevated standard of proof in the inequitable conduct context is paramount," because the penalty, unenforceability, is "so severe."  The Court, ever mindful of the heightened levels of oversight scrutiny the Supreme Court is wont to exercise lately over its decisions, supported this sentiment by reminding us of Supreme Court precedent (specifically, Hazel-Atlas Glass Co. v. Hartford-Empire Co. and Precision Instrument Mfg. Co. v. Automotive Maintenance Machinery Co.).  Courts must be "vigilant in not permitting the defense to be applied too lightly."  "Just as it is inequitable to permit a patentee who obtained his patent through deliberate misrepresentations or omissions of material information to enforce the patent against others, it is also inequitable to strike down an entire patent where the patentee only committed minor missteps or acted with minimal culpability or in good faith."

    Specifically with regard to the deceptive intent prong, the Court noted that "materiality does not presume intent" (they are separate prongs of the analysis), and then cited Molins PLC v. Textron, Inc.:

    [T]he alleged conduct must not amount merely to the improper performance of, or omission of, an act one ought to have performed.  Rather, clear and convincing evidence must prove that an applicant had the specific intent to . . . mislead[] or deceiv[e] the PTO.  In a case involving nondisclosure of information, clear and convincing evidence must show that the applicant made a deliberate decision to withhold a known material reference.

    What is required, said the Court, is a "specific intent to deceive the PTO."

    Since the CAFC recognizes that "direct evidence of deceptive intent is rarely available," the required intent can be inferred from conduct and other "indirect and circumstantial evidence," citing Cargill, Inc. v. Canbra Foods, Ltd., 476 F.3d 1359, 1364 (Fed. Cir. 2007).  But this doesn’t lower the evidentiary requirements; indeed, it appears the Court believes that it raises them.  If a court must deal with inferences, such inferences "must not only be based on sufficient evidence and be reasonable in light of that evidence, but it must also be the single most reasonable inference able to be drawn from the evidence to meet the clear and convincing standard," citing Scanner Technologies Corp. v. ICOS Vision Systems Corp., 528 F.3d 1365 (Fed. Cir. 2008) (emphasis added).

    With regard to the exercise of a court’s equitable discretion in finding inequitable conduct, in the absence of clear and convincing evidence of both materiality and intent a court has no discretion — it cannot find inequitable conduct, according to the Federal Circuit.  Even if a defendant establishes both intent and materiality by clear and convincing evidence, a finding of unenforceability on inequitable conduct grounds is not inevitable.  A court should "look to the equities" and balance all of these equities with the substance of the facts underlying the "clear and convincing" evidence of materiality and intent, "to determine whether the severe penalty of unenforceability should be imposed."  This determination is left to a court’s sound discretion.

    Rj_reynoldsIn this case, the Federal Circuit disagreed that Defendants had shown clear and convincing evidence of intent as to patentee’s conduct in prosecuting the ‘649 patent, and also disagreed that the withheld information was material to the patentability of the ‘401 patent claims.  The Court found that R.J. Reynolds’ "quarantine" theory (of preventing the Banner attorneys from knowing what the Sughrue attorneys knew about the Burton letter and experimental data) was not established by clear and convincing evidence.  The Court found that Star Scientific had proffered other, plausible explanations for changing counsel.  While acknowledging that credibility determinations were properly within the province of the district court and should not be second-guessed by an appellate court, the Federal Circuit also cautioned against shifting the burden from R.J. Reynolds to Star Scientific:  Star Scientific did not bear the burden of rebutting R.J. Reynolds’ evidence unless and until Reynolds had established an intent to deceive by clear and convincing evidence.  "[A] patentee need not offer any good faith explanation unless the accused infringer first carried his burden to prove a threshold level of intent to deceive by clear and convincing evidence."  Here, the Federal Circuit found "major gaps" in the evidentiary bases for R.J. Reynolds’ theory, and accordingly found that the Defendants had not established intent by clear and convincing evidence.

    With regard to the ‘401 patent, the issue was materiality and here the CAFC found that Star Scientific had provided additional information and evidence, including evidence from the litigation, that rendered the Burton letter and experimental data cumulative.  Ironically, key evidence provided by Star Scientific that rendered the undisclosed Burton letter and data cumulative was R.J. Reynolds’ response to one of Star Scientific’s interrogatories, outlining that changing curing conditions to reduce TSNA concentrations in cured tobacco was known in the prior art.

    Judge_michel
    So far, it has been the Court’s veteran judges, like Judge Rader and Chef Judge Michel (at right), who have hewed more closely to the limitations on inequitable conduct set forth in Kingsdown and Molins.  The Court has shown a willingness in other areas, such as claim construction, to revisit and reaffirm its jurisprudence en banc when panels of the Court have significant drifted from those principles.  Perhaps the time is approaching when the Court will decide to revisit and reaffirm its Kingsdown and Molins principles for determining whether a patent should be deemed unenforceable for being improperly procured through inequitable conduct.

    Star Scientific, Inc. v. R.J. Reynolds Tobacco Co. (Fed. Cir. 2008)
    Panel: Chief Judge Michel and Circuit Judges Schall and Dyk
    Opinion by Chief Judge Michel