• CalendarApril 19, 2018 – "Overcoming § 101 Rejections for Computer and Electronics Related Patents — Leveraging USPTO Guidance and Recent Decisions to Meet 101 Patent Eligibility Requirements" (Strafford) – 1:00 to 2:30 pm (EDT)

    April 19, 2018 – "When All Else Fails: How, When and Why to Terminate an IP License" (Technology Transfer Tactics) – 1:00 to 2:00 pm (ET)

    April 23-24, 2018 – Paragraph IV Disputes conference (American Conference Institute) – New York, NY

    April 24, 2018 – "Trade Secrets Update 2018: Year Two of the DTSA" (McDonnell Boehnen Hulbert & Berghoff LLP) – 10:00 am to 11:15 am (CT)

    April 26, 2018 – "Patent Eligibility, Duty to Disclose and More: USPTO Manual of Patent Examining Procedure New Guidance" (Strafford) – 1:00 to 2:30 pm (EDT)

    April 27, 2018 – Ethics in the Practice of Intellectual Property Law (John Marshall Law School Center for Intellectual Property, Information & Privacy Law) – 12:30 to 5:15 pm, Chicago, IL

    May 1, 2018 – "Patent Inventorship: Best Practices for Determination and Correction — Distinguishing Between Inventor and Contributor; Navigating Joint Inventorship, Disclosure of Ownership, Real Party in Interest" (Strafford) – 1:00 to 2:30 pm (EDT)

    May 2, 2018 – "Recent Developments in Double Patenting: ODP Challenges and Considerations" (The Knowledge Group) – 12:00 to 1:30 pm (ET)

    May 3, 2018 – "Patent Ownership Rights: Structuring Assignment and Employment Contracts — Key Provisions, Implications for Litigation, Recent Court Treatment" (Strafford) – 1:00 to 2:30 pm (EDT)

    May 3, 2017 – "The Very Essence of Romance is Uncertainty" (Intellectual Property Owners Association European Practice Committee) – Amsterdam, Netherlands

    June 25-27, 2018 – Summit on Biosimilars (American Conference Institute) – New York, NY

  • ACIAmerican Conference Institute (ACI) will be holding is 9th Annual Summit on Biosimilars on June 25-27, 2018 in New York, NY.  Patent Docs author Kevin Noonan is a co-chair of this conference.  ACI faculty will help attendees:

    • Explore the current initiatives to foster innovation and lower healthcare costs from the current administration;
    • Review current case law that will impact the biologics marketplace, such as Amgen v. Hospira and Amgen v. Sanofi;
    • Compare various strategies for biosimilar manufactures and reference product sponsors in view of the Supreme Court's Sandoz v. Amgen case;
    • Consider strategic decisions related to the use of IPRs in the biosimilars context;
    • Examine the status of interchangeability and a review of state legislation for pharmacy-level substitution;
    • Review the impact of the FDA's naming guidance; and
    • Analyze the ethical concerns facing the biologics and biosimilars marketplace.

    In particular, ACI faculty will offer presentations on the following topics:

    • Biosimilars on the Hill: Policy and Legislative Updates
    • Regulatory Year in Review and Predictions for the Future
    • Update on Hot-Button Litigation Issues and the Impact on the Biologics Market and Strategies
    • NOW . . . You Can Dance If You Want to
    • Navigating through Biosimilars IPRs
    • Perfecting Your Biologics Prosecution Strategies
    • Interchangeability for Biosimilars: Envisioning the Future
    • Naming and Labeling Considerations for Biosimilar Products
    • Market Access, Pricing, and Reimbursement
    • Evaluating Ethical Concerns for the Biologics Industry

    In addition, two post-conference workshops will be offered on June 27, 2018, from 9:00 am to 12:00 noon and 1:30 to 4:30 pm, respectively.  The first workshop is entitled "Untangling the Inner Workings of IPRs for Biosimilars," and the second workshop is entitled "Gaining a Global Perspective: Tips and Strategies for Establishing and Maintaining an International Biosimilars Portfolio."

    An agenda for the conference and additional information regarding the workshops can be found here.  A complete brochure for this conference, including an agenda, detailed descriptions of conference sessions, list of speakers, and registration form can be obtained here.

    The early-bird registration fee if paid before April 20, 2018 is $1,995 (conference alone), $2,595 (conference and one workshop), and $2,995 (conference and both workshops).  Special rates are available for in-house counsel (see brochure).  Patent Docs readers are entitled to a 10% discount off of registration using discount code P10-999-PTD18.  Those interested in registering for the conference can do so here, by e-mailing CustomerService@AmericanConference.com, or by calling 1-888-224-2480.

    Patent Docs is a media partner of ACI's 9th Annual Summit on Biosimilars.

  • Strafford #1Strafford will be offering a webinar entitled "Patent Inventorship: Best Practices for Determination and Correction — Distinguishing Between Inventor and Contributor; Navigating Joint Inventorship, Disclosure of Ownership, Real Party in Interest" on May 1, 2018 from 1:00 to 2:30 pm (EDT).  Jill K. MacAlpine and Amanda K. Murphy of Finnegan Henderson Farabow Garrett & Dunner will provide guidance for patent counsel on identifying and determining inventorship, offer best practices for correcting errors regarding inventorship, offer perspectives gained from working with the AIA since it was passed, and outline lessons from recent court decisions.  The webinar will review the following issues:

    • What key information does counsel need to determine inventorship?
    • What are the steps for counsel when inventorship must be corrected?
    • What is the AIA’s impact on an inventorship determination?

    The registration fee for the webcast is $297.  Those interested in registering for the webinar, can do so here.

  • JMLSThe John Marshall Law School Center for Intellectual Property, Information & Privacy Law will be holding its 9th Annual Program on Ethics in the Practice of Intellectual Property Law from 12:30 to 5:15 pm on April 27, 2018 in Chicago, IL.  The conference will consist of the following sessions:

    • What IP Lawyers Should Know About ARDC Proceedings and Client Complaints
    • Ethical Issues in Providing Pro Bono IP Representation
    • Trademark Scams and Unauthorized Practice of Trademark Law
    • Mental Health and Addiction Issues Among Lawyers: A Focus on Clinical Depression and Substance Use Disorders

    Additional information about the program can be found here.  Those interested in registering for the conference online can do so here; the registration fee is $195 (general registration); JMLS Students, Faculty, Staff, and IP Advisory Board Members can register for free.

  • Strafford #1Strafford will be offering a webinar entitled "Patent Ownership Rights: Structuring Assignment and Employment Contracts — Key Provisions, Implications for Litigation, Recent Court Treatment" on May 3, 2018 from 1:00 to 2:30 pm (EDT).  Eman Ahmed-Fakhry, Senior Counsel, Hospital Therapies Department, Mallinckrodt Pharmaceuticals; Anne Elise Herold Li of Crowell & Moring; and Robert Schaffer of Troutman Sanders will guide counsel on securing patent ownership to inventions created by employees or independent contractors, discuss essential provisions and strategies when structuring employee-assignment and contractor agreements and discuss the implications for litigation when assignment is not explicit and other pitfalls in structuring these agreements.  The webinar will review the following issues:

    • What key provisions should counsel include in employee assignment agreements?
    • What hurdles must counsel watch for to establish ownership of employee or contractor-created inventions?
    • What strategies should counsel employ to ensure ownership of employee or contractor-created inventions?

    The registration fee for the webcast is $297.  Those interested in registering for the webinar, can do so here.

  • IPO #2The Intellectual Property Owners Association (IPO) European Practice Committee will be hosting a one-day conference entitled "The Very Essence of Romance is Uncertainty" on May 3, 2017 in Amsterdam, Netherlands.  The conference will include sessions on the following topics:

    • "Shapes Of Things to Come" — Current Legislative \and Juridical Trends in the US
    • "My Weakness is None of Your Business" — The Present and Future of Discovery and Trade Secrets
    • "Traummaschine" — What Future Does the UPC Hold for Us?
    • "Wir Sind De Roboter" — IP and Legal Tech

    A program for the conference, including an agenda and list of speakers can be found here.  The registration fee for the conference is $250 (IPO member) or $300 (non-member).  Those interested in registering can do so here.

  • The Knowledge GroupThe Knowledge Group will offer a webcast entitled "Recent Developments in Double Patenting: ODP Challenges and Considerations" on May 2, 2018 from 12:00 to 1:30 pm (ET).  Russell S. Timm of Womble Bond Dickinson (US) LLP, Carl A. Morales of Dechert LLP, and Bonnie Weiss McLeod of Cooley LLP will address the following topics:

    • ODP — Trends and Developments
    • Risks for Patent Owners
    • Challenges and Considerations
    • Recent Double Patenting Court Rulings
    • Best Practices to Protect Against ODP Issues

    The registration fee for the webcast is $99.  Those interested in registering for the webinar can do so here.

  • By Andrew Williams

    Federal Circuit SealWhich parties to an IPR proceeding have standing to either appeal or participate in an appeal from an adverse final written decision by the Board?  The Federal Circuit had previously held that a petitioner that did not otherwise have Article III standing could not appeal an adverse decision (Phigenix, Inc. v. Immunogen, Inc.), but that a successful petitioner was "not constitutionally excluded from appearing in court to defend" a decision (Personal Audio, LLC v. Electronic Frontier Foundation).  Today, in Luitpold Pharmaceuticals, Inc. v. Pharmacosmos A/S, the Federal Circuit answered in the negative the question whether a petitioner otherwise without standing could cross-appeal a final written decision in which some of the claims were determined to be patentable.  In a two-page order, the Court stated that "[b]ecause Pharmacosmos has not established an injury fact sufficient to confer Article III standing," it was dismissing the case.  However, because the order is nonprecedential, and more importantly because there was no discussion or analysis as to why Pharmacosmos lacked standing, it is unclear what the broader implications of this case will be.  Nevertheless, by looking at the underlying briefing and oral argument, we might be able to glean some information about the contours of what is required to find petitioner standing for IPR proceedings.

    How did we get here?  The language of 35 U.S.C. § 141(c) states that any party "who is dissatisfied with the final written decision" of the Board "may appeal the Board's decision" to the Federal Circuit.  Nevertheless, the Federal Circuit's Consumer Watchdog v. Wisconsin Alumni Research case in the inter partes reexamination context appeared to be the writing on the wall for petitioners desiring to appeal IPR decisions that did not have Article III standing.  Of course, the Federal Circuit made it clear in the Phigenix case that standing is required for a petitioner to appeal an adverse final written decision.  Important in that decision was the fact that the petitioner/appellant was "not engaged in any activity that would give rise to a possible infringement suit."  The Court has also held that as long as the appellant has standing, a petitioner does not require independent standing to participate in the appeal.  In the Personal Audio case, the public interest group Electronic Frontier Foundation ("EFF") had crowd-sourced both the cost of filing an IPR petition against Personal Audio's podcasting patent (made famous (or infamous) by the NPR podcast "Planet Money"), and the technological substance found within the petition.  Other than coordinating the effort, filing, and participating in the IPR proceeding, the EFF had no interest in the case that could be used to establish the Article III case-or-controversy requirement.  Nevertheless, because Personal Audio, "the party invoking judicial review," had "experienced an alteration of 'tangible legal rights,'" sufficient to confer standing, the EFF was not excluded from the appeal.

    So why did Pharmacosmos think that it had standing to cross-appeal its adverse decision from the Board?  One attempt to distinguish this case from Phigenix was in noting that the Court already had jurisdiction over Luitpold's appeal of the same patents and that the two claims Pharmacosmos was appealing were related to these other claims by subject matter.  In other words, it was arguing part Personal Audio and part judicial efficiency.  However, Personal Audio was not applicable here because nothing was stopping Pharmacosmos from participating as an appellee.  This issue was its cross appeal.  And Luitpold had identified numerous Federal Circuit cases that stood for the proposition that the standing requirements applied equally to "appeals" and "cross appeals."  As such, even if there would be judicial economy, it would be irrelevant if there did not exist standing in the first place.

    In addition, Pharmacosmos attempted to take Phigenix head-on by distinguishing the cases on their facts.  Pharmacosmos argued that the Phigenix company was a discovery-stage biotechnology research company that did not market any products.  Instead, Pharmacosmos itself was a well-established company with a number of marketed products and in direct active market competition with Luitpold.  The patent at issue was U.S. Patent No. 7,754,702, entitled "Methods and Compositions for Administration of Iron," which claims methods of treating diseases, disorders, or conditions "characterized by iron deficiency or dysfunctional iron metabolism resulting in reduced bioavailability of dietary iron . . . ."  The '702 patent is listed in the Orange Book as covering the Luitpold product Injectafer®, along with three additional patents, including the grandchild of the '702 patent, U.S. Patent 8,895,612.  Nevertheless, Pharmacosmos does not yet sell a product in the U.S. that would fall within the scope of those claims.  Even though it is marketing its own iron isomaltoside product in Europe, Monofer®, Pharmacosmos is still conducting clinical trials in the U.S. to obtain FDA approval.  Moreover, Pharmacosmos' relationship with its former development partner, Helsinn Healthcare S.A., ended, and it was still seeking a new commercialization partner for the U.S.

    Nevertheless, Luitpold had sent a warning letter to Pharmacosmos regarding its development of Monofer® in the U.S.  This occurred shortly after Pharmacosmos and Helsinn announced their partnership in January 2015.  Within a month, Luitpold sent warning letters claiming infringement, but the letters only mentioned the grandchild '612 patent not the '702 patent.  Luitpold pointed out that the warning letter was irrelevant because it did not mention the '702 patent.  However, Pharmacosmos maintained its relevance because the two patents had allegedly overlapping claims.  And even though there is no opinion or discussion in the order regarding this warning letter, the Federal Circuit apparently agreed with Luitpold that it was not relevant.  For example, during oral argument, counsel for Pharmacosmos noted that it had "a little bit of an additional hurdle to get through to convince the Court that the assertion of other patent rights which had substantially similar claim elements . . . would create a reasonable apprehension on the part of [Party] that it will be sued."  The Court interrupted in the middle of this statement with the snide (but telling) remark:  "Just a little bit."

    The other stumbling block that Pharmacosmos could not overcome was the Sandoz v. Amgen case, in which the Court held that a biosimilar maker did not have standing to bring a declaratory judgement action against a BLA holder prior to the filing of an aBLA with the FDA.  Luitpold argued that the Pharmacosmos situation was even worse, because its clinical studies were expected to take several years.  During Oral Argument, the Federal Circuit seemed equally skeptical that this case was any different than Sandoz.  In fact, when pressed, Pharmacosmos' counsel could only point to the warning letter as a distinction between the two cases.  But again, this letter mentioned different patent rights, not those at issue in the present IPR.  The Court is currently considering another case in which a biosimilar manufacturer filed an IPR before submitting its aBLA, so we may see additional analysis of the difference between the IPR setting and the DJ jurisdiction of Sandoz v. Amgen.  However, for the present case, any such distinction was insufficient for the Court to find Article III standing for the Pharmacosmos cross-appeal.

    This case, and others like it, will likely be a topic of discussion at the American Conference Institute's 12th Annual Paragraph IV Disputes conference on April 23-24, 2018 in New York, NY.  As a reminder, this author will be in attendance, so if you are attending, please say hello.  Patent Docs readers are entitled to a 10% discount off of registration using discount code P10-999-PTD18, but hurry because space is limited and registration will be closing soon.

    Luitpold Pharmaceuticals, Inc. v. Pharmacosmos A/S (Fed. Cir. 2018)
    Nonprecedential disposition
    Panel: Chief Judge Prost and Circuit Judges Wallach and Taranto
    Per Curiam Order

  • By Aaron Gin

    "The first and only autonomous AI system authorized by the FDA"

    FDAOn April 11, 2018, the U.S. Food and Drug Administration (FDA) permitted marketing of a medical device that utilizes artificial intelligence to diagnose eye disease in diabetic adults.  The device, called IDx-DR from the company IDx, screens patients for diabetic retinopathy using deep learning algorithms.  The screening involves standard retinal imaging, takes less than a minute, and can be performed without a clinician's interpretation of the images or results.  Accordingly, IDx-DR may be used in primary care offices for early detection of retinopathy, which can lead to vision impairment and blindness.

    IDx founder Michael Abramoff, a retinal specialist at the University of Iowa, told Science News that the medical device is unique because it operates autonomously and there is no specialist "looking over the shoulder of the algorithm."  "It makes the clinical decision on its own."

    The FDA based its decision to permit marketing of IDx-DR, in part, on a clinical trial of the system involving the screening recommendations and corresponding retinal images from over 800 diabetic patients at ten different primary care sites.  The study indicated that IDx-DR correctly identified the presence of more than mild diabetic retinopathy 87.4% of the time and correctly identified patients with less than mild diabetic retinopathy 89.5% of the time.  The former group was referred to a specialist and the latter group was scheduled for a checkup in 12 months.

    Tweets from FDA Commissioner Indicate AI Push

    On the same day as the IDx-DR announcement, FDA Commissioner Scott Gottlieb M.D. unleashed a string of tweets that strongly endorsed AI-based health care solutions.  Based on Dr. Gottlieb's comments, it appears that the FDA may be currently accelerating review of AI-based systems.  Looking ahead, Gottlieb also signaled that AI-specific fast track regulatory pathways are under development.

    Despite such relaxed AI regulations at the FDA, however, Dr. Gottlieb tweeted that the agency's approach would maintain consumer safety by establishing "appropriate guardrails."  Based on Dr. Gottlieb's comments, it will be interesting to track the FDA approval rate and timeline of AI-based healthcare solutions.  Additionally, in the case of new AI-specific regulatory pathways, time will tell what "guardrails" the FDA will put in place to maintain adequate safety as future AI innovations are made available to patients and providers.  Data privacy, algorithmic transparency, and "unbiased" learning datasets are just a few broad areas in which the FDA might regulate artificial intelligence as applied to health care.

    For additional information regarding this topic, please see:

    In the future, an AI may diagnose eye problems (Science News, March 4, 2018)
    IDx-DR (IDx LLC Website)
    FDA permits marketing of artificial intelligence-based device to detect certain diabetes-related eye problems (FDA News Release, April 11, 2018)
    • Scott Gottlieb, M.D. – Commissioner, U.S. Food and Drug Administration (Twitter: @SGottliebFDA)

  • By Andrew Williams

    USPTO SealThe U.S. Patent and Trademark Office appears to have taken the position that neither party has the burden of persuasion with regard to Motions to Amend after the Aqua Products v. Matal en banc decision (see "Motions to Amend at the PTAB — Does Anyone Have the Burden (And Will That Change)?").  It was unclear, however, whether this position would have any practical impact for parties appearing before the Patent Trial and Appeal Board.  Correspondingly, the Board's grant of two Motions to Amend last month is revealing.  These are the first two motions that were granted outright since Aqua Products, both of which occurred in IPRs entitled Apple Inc. v. Realtime Data LLC, with both being directed to U.S. Patent No. 8,880,862.  Before this, the Board had only granted-in-part two additional motions:  (1) Taiwan Semiconductor Manufacturing Co. v. Godo Kaisha IP Bridge (IPR2016-01249) at the end of last year (see "More Aqua Products Fallout — Taiwan Semiconductor Manufacturing Co. v. Godo Kaisha IP Bridge"); and (2) Polygroup Ltd. v. Willis Electric Co. (IPR2016-01613) in February (although to be fair, the contingent part of this motion was denied because the challenged claims were found to not be unpatentable).  Clearly, the flood gates have not been opened with respect to claim amendments in IPR proceedings because there have still been many more motions denied than granted (even in part).  But these two Apple v. Realtime Data cases could be instructive for Patent Owners seeking to amend claims in a post-Aqua Products world, especially with respect to whether the petitioner bears the burden with regard establishing the unpatentability of the substitute claims.

    The technology at issue in the '862 patent was "[s]ystems and methods for providing accelerated loading of operating system and application programs upon system boot or application launch . . . ."  Id., Abstract.  As explained in one of the motion decisions, Realtime Data proposed adding four limitations to the issued claims in response to the instituted grounds:  "(1) preloading a portion of boot data; (2) into a volatile memory, the portion of boot data in the compressed form being associated; (3) wherein the preloading comprises transferring the portion of boot data in the compressed form into the volatile memory, and wherein the preloading occurs during the same boot sequence in which a boot device controller receives a command over a computer bus to load the portion of boot data; and (4) accessing the preloaded portion of the boot data in the compressed form from the volatile memory."  IPR2016-01737, Paper 57 at 46-47.  The Patent Owner argued in the motions that none of the cited prior art references taught or suggested "preloading" of compressed boot data into a "volatile" memory.

    The Board first determined that Realtime Data had satisfied 37 C.F.R. § 42.121.  In IPR2016-01737, the Patent Owner proposed substituting 55 claims for the 55 challenged claims, while in IPR2016-01738, the Patent Owner proposed 45 claims to substituted for the 45 challenged claims.  Nevertheless, because there was a one-for-one correspondence, the number of claims was determined to be reasonable.  In addition, the Patent Owner had identified support in the original specification for the newly added limitations, for example where support could be for the limitation that the preloading may occur in volatile memory.  Moreover, the Board determined that these limitations were narrowing and did not add new subject matter.  Finally, the Board found that these proposed narrowing limitations were in direct response to the instituted grounds of unpatentability.  Correspondingly, the Patent Owner had met its burden with regard to the statutory and procedural requirements for the Motion to Amend.

    The Board then turned to whether the proposed substitute claims were patentable over the prior art.  At first, the Board appeared to again suggest that neither party had the burden by citing to Aqua Products and the Chief Judge's guidance in explaining the requirement that unpatentability be determined based on the "entirety of the record, including any opposition made by the petitioner."  See, e.g., IPR2016-01737, Paper 57 at 46.  However, two sentences later, the Board seemed to place the burden squarely on the petitioner when it "determine[d] that Petitioner fail[ed] to establish that proposed substitute claims 118-173 are obvious over" the cited art.  Id.     

    Even more telling was a discussion by the Board of the claim limitation for "preloading" boot data into "volatile" memory.  The Patent Owner had contended that even though one of the cited references, Zwiegincew, discussed the use of "boot" in its background section, it did not do so in the context of preloading boot data into volatile memory.  The Patent Owner also pointed out that two of the other references, Burrow and Dye, did not teach or suggest this limitation.  In fact, Patent Owner noted that Petitioner cited these references for their teaching regarding compression/decompression, and not for the newly added claim limitation.  The Petitioner, on the other hand, did not address any of these three references individually.  However, instead of stating that the claim limitation was not met by the cited art after reviewing "the entirety of the record," the Board instead concluded that it found "that Petitioner fail[ed] to establish that Zwiegincew, Burrow or Dye teach or suggest 'preloading' boot data into 'volatile' memory."  Id.  at 51.

    Therefore, even though the Board did conclude its grant of the Motion to Amend by noting "that when considering the entirety of the record before us, we determine that the preponderance of the evidence fails to establish that the proposed substitute dependent claims are unpatentable," it did appear to put the burden on petitioner to reach that conclusion.  It is unclear whether this case is an aberration, or whether there will be more emphasis on the burdens assigned to petitioners in Motions to Amend going forward.  It is also unclear whether this case will make it easier for patent owners to get similar motions granted in the future.  Nevertheless, some of the language found in these two cases should be considered persuasive for patent owners to use going forward.

    Apple, Inc. v. Realtime Data LLC, Case IPR2016-01737 (PTAB 2018)
    Panel: Administrativbe Patent Judges Stpehens, Braden, and Chung
    Final Written Decision by Administrative Patent Judge Braden

    Apple, Inc. v. Realtime Data LLC, Case IPR2016-01738 (PTAB 2018)
    Panel: Administrativbe Patent Judges Stpehens, Braden, and Chung
    Final Written Decision by Administrative Patent Judge Braden