• Calendar

    July 30-31, 2012 – Freedom to Operate*** (American Conference Institute) – Philadelphia, PA

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

    August 2, 2012 – USPTO Post-Grant Proceedings:  Meeting the New Requirements for Post-Grant and Inter Partes Reviews and Supplemental Examination (Strafford) – 1:00 – 2:30 pm (EDT)

    September 9-11, 2012 – IPO Annual Meeting (Intellectual Property Owners Association) – San Antonio, TX

    September 10-12, 2012 – Business of Biosimilars & Generic Drugs (Institute for International Research) – Boston, MA

    September 20-21, 2012 – FDA Boot Camp*** (American Conference Institute) – Boston, MA

    September 24-25, 2012 – Biosimilars and Biobetters*** (SMi) – London, UK

    September 25-26, 2012 – EU Pharma Regulatory Law*** (C5) – Brussels, Belgium

    October 10-11, 2012 – Maximizing Pharmaceutical Patent Lifecycles*** (ACI) – New York, NY

    October 10-11, 2012 – Biotech & Pharmaceutical Patenting*** (C5) – London, UK

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

  • New York #2American Conference Institute (ACI) will be holding its 13th Annual Maximizing Pharmaceutical Patent Lifecycles conference on October 10-11, 2012 in New York, NY.  The conference will allow attendees to:

    • Understand how the patent cliff will impact innovation and alter the industry dynamic between brand names and generics;
    • Explore how generic user fees and other new and revised items under PDUFA will affect R&D and market entry;
    • Demystify the provisions of the America Invents Act and learn how post-grant review, inter partes review, and institution of a global prior art regime will impact life cycle management;
    • Analyze the recently issued FDA regulations on biosimilars and comprehend how the further implementation of BPCIA will affect pharmaceutical patent life cycle management strategies;
    • Assess how the combined evolution of prior art obvious and obvious-type double patenting are influencing the future of secondary patents;
    • Evaluate patent life cycle strategies relative to personalized medicine in light of Prometheus;
    • Examine the link between inducement and divided infringement actions relative to methods of use claims for pharmaceutical patents;
    • Appreciate how Caraco has affected Orange Book listings and redefined the relationship between a drug's patent, label and use code;
    • Explore forfeiture rulings post-Lipitor; and
    • Navigate new safe harbor dilemmas for both general screening and research tool patents.

    Brochure MaximizingIn particular, ACI's faculty will offer presentations on the following topics:

    • From product development to patent portfolio management: Patent life cycle strategies for a post-AIA world;
    • An industry perspective on implementation of the AIA, new PTO proceedings, and their collective impact on life cycle management;
    • Preparing for the implementation of the FDA's biosimilars pathway and its effects on life cycle planning;
    • Exploring the latest regulatory conundrums affecting pharmaceutical patent life cycle strategies;
    • Personalized medicine and patent life cycle considerations in light of Prometheus and other recent challenges to subject matter patentability, written description, and more;
    • Employing strategies to avoid findings of obviousness: Legal analysis and practical applications for brand names and generics;
    • Inequitable conduct post-Therasense and how it impacts life cycle planning;
    • USPTO keynote: The brave new world of patent reform and its impact on pharmaceutical patents — to be presented by USPTO Deputy Director Teresa Stanek Rea;
    • Understanding how Caraco has redefined the relationship between pharmaceutical patents, labels, and use codes;
    • Analyzing method claims and the madness over recent and pending inducement and divided infringement cases;
    • Exclusivities and forfeitures: New developments, controversies and related concerns;
    • An update on FDA activities impacting pharmaceutical patent life cycle planning;
    • Safe harbor or stormy port?  Calming the legal tempest left by Proveris; and
    • Understanding the importance of Rx to OTC switches to the future of pharmaceutical patent life cycle management.

    Two pre-conference workshops will be offered on October 9, 2012.  The first, entitled "Working Group Session: Assessing the Impact of New PTO Procedures Under the AIA on Hatch-Waxman Strategies Relative to Patent Life Cycle Management" will be held from 9:00 am to 12:30 pm.  The second, entitled "PTA-PTE Boot Camp: Basic Training in the Essentials of Patent Term Adjustment and Patent Term Restoration for Patent Lawyers Serving the Biopharmaceutical Industry" will be held from 2:00 pm to 5:30 pm.

    The agenda for the Maximizing Pharmaceutical Patent Lifecycles conference can be found here, and additional information regarding the wrokshops 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.

    ACI - American Conference InstituteThe registration fees are $2,295 (conference only), $2,895 (conference plus one workshop), or $3,495 (conference plus two workshops).  Those registering by September 10, 2012 will receive a $200 discount off the registration fee, and those registering on or before August 13, 2012 will receive a $300 discount.  Patent Docs readers who reference the discount code "PD 200" will receive $200 off the current price tier when registering.  Those interested in registering for the conference can do so here, by e-mailing CustomerService@AmericanConference.com by calling 1-888-224-2480, or by faxing a registration form to 1-877-927-1563.

    Patent Docs is a media partner of ACI's Maximizing Pharmaceutical Patent Lifecycles conference.

  • LondonC5 (UK) will be holding its 23th Annual Forum on Biotech & Pharmaceutical Patenting on October 10-11, 2012 in London, UK.  The conference will allow attendees to:

    • Discover competitive patent filing strategies, tactics, and implications of recent case law in Europe and the U.S.;
    • Avoid infringing anti-competition laws by tailoring agreements and learning about the key factors the European Commission look for when conducting their investigations;
    • Develop patent strategies to optimize patent lifecycles and extend market dominance;
    • Stay one step ahead of competitors by discovering the latest trends and priorities of the EPO and national patent offices;
    • Avoid patent infringement when conducting clinical trials and how to use the Bolar Exemption effectively; and
    • Obtain Supplementary Protection Certificates (SPCs) to extend patent lifecycles following Novartis.

    BrochureIn particular, C5 faculty will offer presentations on the following topics:

    • Examining what is now patentable in light of Brüstle:  The implications for human embryo stem cell research;
    • Optimising your SPC strategies & utilising the paediatric extension: Prolonging your patent life cycles and cementing your market position;
    • Keynote presentation from the AIPPI;
    • Taking advantage of the proposed EU patent court & European patent reform to streamline your IP strategy;
    • Avoiding patent infringements in your clinical trials by utilising the Bolar Exemption;
    • The implications of Prometheus on the patent eligibility of your gene patents;
    • Gain a competitive advantage by aligning your patent strategies with the EPO's latest initiatives & priorities;
    • Emerging markets focus afternoon: Successfully overcoming hurdles to the protection & management of IP assets in emerging markets;
    • Overcoming regulatory & strategic hurdles to enforcement of your patents in Asia;
    • Surmounting the problems arising from inconsistent provisions in Brazil's paradoxical patent law to successfully protect your IP assets;
    • Tips, traps and techniques for successfully obtaining & protecting your patents in India & the implications of the first compulsory licence issued in India;
    • The impact of the us patent reform on European biotech and pharma companies: Updating and strengthening your global patent strategies;
    • The antibody patenting conundrum;
    • Obtaining injunctive relief: Provisional enforcement of rights before trial;
    • Gain a competitive edge by understanding how the new biosimilar regulatory guidelines in Europe & the U.S. will affect your patent strategy;
    • Practical steps to take to protect your patent portfolio following Occlude;
    • Minimise the risk of your patent strategy falling foul of anti-competition laws in the U.S. and the EU in an era of heightened regulatory scrutiny;
    • Alternative models for protecting your knowhow & intellectual assets: Lessons to be learned from other technology sectors; and
    • Minimising the cost of potential litigation through alternative methods of funding.

    In addition, two pre-conference workshops will be held on October 9, 2012.  The first, entitled "IP Due Diligence Procedure: Comprehensive Practical Guide to Best Practice," will be offered from 9:00 am to 12:00 pm, and will provide in-depth, critical insights into the often overlooked aspect of the procedure for conducting IP due diligence in M&A, joint venture, and licensing transactions.  The second, entitled "Matters to Be Aware of When Reviewing Patent Settlement Agreements & Distribution Agreements to Minimise the Risk of Infringing Anti-Competition Laws," will be offered from 1:30 to 4:00 pm, and will guide attendees through settlement agreements and provide practical and strategic tips for drafting and reviewing these agreements to ensure you do not fall foul of anti-competition laws in the U.S. or the EU.

    A complete brochure for the Biotech & Pharmaceutical Patenting conference, including an agenda, detailed descriptions of conference sessions, list of speakers, and registration form can be obtained here.

    C5The registration fee is £1595 (conference alone), £2095 (conference plus one workshop), or £2495 (conference and both workshops).  Those registering on or before September 12, 2012 will receive a £100 discount.  Those interested in registering for the conference can do so here, by e-mailing registrations@C5-Online.com, by calling +44 20 7878 6888, or by faxing a registration form to +44 20 7878 6885.

    Patent Docs is a media partner of the C5 Biotech & Pharmaceutical Patenting conference.

  • By Kevin E. Noonan

    European Union (EU) FlagAgain in only the span of a few months, the views of the Advocate General of the European Court of Justice (ECJ) have been adopted by Court.  Previously, this pattern resulted in a ban on patenting human embryonic stem cells (see "European Court of Justice Renders Stem Cell Decision").  Last Thursday, the Court agreed with the AG that Supplementary Protection Certificates (SPCs) should be made available for new pharmaceutical uses for known products, providing innovator drug companies with an additional five years of patent protection under circumstances where patent term had been running during the time taken for regulatory approval.

    Neurim PharmaceuticalsThe case came to the ECJ from the UK Court of Appeals, after the Intellectual Property Office (IPO) rejected grant of an SPC to Neurim Pharmaceuticals Ltd., which had developed a formulation of melatonin for treating insomnia.  (Melatonin, produced in the pineal gland, has long been known to be involved in maintaining circadian rhythms in animals including humans.)  In this case, the grounds for the IPO's denial of SPC protection was a previous approval of a different melatonin formulation for use in sheep breeding; under the IPO's interpretation of the law, the sheep use constituted a "first medical use" of the compound, thus precluding grant of an SPC on the insomnia formulation to Neurim.

    Five Questions were Presented to the ECJ from the UK Court of Appeals:

    1.  In interpreting Article 3 of Regulation 469/2009 ("the SPC Regulation") when a marketing authorisation (A) has been granted for a medicinal product comprising an active ingredient, is Article 3(d) to be construed as precluding the grant of an SPC based on a later marketing authorisation (B) which is for a different medicinal product comprising the same active ingredient where the limits of the protection conferred by the basic patent do not extend to placing the product the subject of the earlier MA on the market within the meaning of Article 4?

    2.  If the grant of the SPC is not precluded, does it follow that in interpreting Article 13(1) of the SPC Regulation, "the first authorisation to place the product on the market in the Community" needs to be an authorisation to place a medicinal product on the market within the limits of the protection conferred by the basic patent within the meaning of Article 4?

    3.  Are the answers to the above questions different if the earlier marketing authorisation has been granted for a veterinary medicinal product for a particular indication and the later marketing authorisation has been granted for a medicinal product for human use for a different indication?

    4.  Are the answers to the above questions different if the later marketing authorisation required a full application for marketing approval in accordance with Article 8 (3) of Directive 2001/83/EC (formerly a full application under Article 4 of Directive 65/65/EEC)?

    5.  Are the answers to the above questions different if the product covered by authorisation (A) to place the corresponding medicinal product on the market is within the scope of protection of a different patent which belongs to a different registered proprietor from the SPC applicant?

    In May, Advocate General Verica Trstenjak promulgated an Opinion on the matter, concluding that a proper interpretation of the law would entitle Neurim to an SPC on its insomnia formulation.  The Opinion was set forth as a response to a request for clarification of the law from the UK IPO.  The Opinion cast the inquiry as whether "authorisation to place the product on the market as a medicinal product within the meaning of letter (b) must be the first authorisation to place that product on the market as a medicinal product."  The Opinion also set forth the relevant provisions of the law:

    Article 1 of Regulation No 1768/92, which is entitled 'Definitions', provides:

    'For the purposes of this Regulation:

    (a)    "medicinal product" means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

    (b)    "product" means the active ingredient or combination of active ingredients of a medicinal product;

    (c)    "basic patent" means a patent which protects a product as defined in (b) as such, a process to obtain a product or an application of a product, and which is designated by its holder for the purpose of the procedure for grant of a certificate;

    (d)    "certificate" means the supplementary protection certificate;

    3.    Articles 3 to 5 of Regulation No 1768/92 read as follows:

    'Article 3 – Conditions for obtaining a certificate

    A certificate shall be granted if, in the Member State in which the application referred to in Article 7 is submitted and at the date of that application:

    (a)    the product is protected by a basic patent in force;

    (b)    a valid authorisation to place the product on the market as a medicinal product has been granted in accordance with Directive 65/65/EEC or Directive 81/851/EEC, as appropriate;

    (c)    the product has not already been the subject of a certificate;

    (d)    the authorisation referred to in (b) is the first authorisation to place the product on the market as a medicinal product.

    Article 4 – Subject-matter of protection

    Within the limits of the protection conferred by the basic patent, the protection conferred by a certificate shall extend only to the product covered by the authorisation to place the corresponding medicinal product on the market and for any use of the product as a medicinal product that has been authorised before the expiry of the certificate.

    Article 5 – Effects of the certificate

    Subject to the provisions of Article 4, the certificate shall confer the same rights as conferred by the basic patent and shall be subject to the same limitations and the same obligations.'

    4.    Article 7 of Regulation No 1768/92, which is entitled 'Application for a certificate', provides:

    '1.    The application for a certificate shall be lodged within six months of the date on which the authorisation referred to in Article 3(b) to place the product on the market as a medicinal product was granted.

    2.    Notwithstanding paragraph 1, where the authorisation to place the product on the market is granted before the basic patent is granted, the application for a certificate shall be lodged within six months of the date on which the patent is granted.

    5.    Article 13 of Regulation No 1768/92, which is entitled 'Duration of the certificate', provides:

    '1.    The certificate shall take effect at the end of the lawful term of the basic patent for a period equal to the period which elapsed between the date on which the application for a basic patent was lodged and the date of the first authorisation to place the product on the market in the Community reduced by a period of five years.

    2.    Notwithstanding paragraph 1, the duration of the certificate may not exceed five years from the date on which it takes effect.

    In its synopsis of the facts, the Opinion sets forth the claim of Neurim's European Patent for which the SPC was requested:

    A pharmaceutical formulation, for use in correcting a melatonin deficiency or distortion in the plasma melatonin level and profile in a human subject, which comprises melatonin in combination with at least one pharmaceutical carrier, diluent or coating, wherein the melatonin is present in the formulation in controlled-release form adapted to release melatonin following administration to a human patient, over substantially the whole of a single nocturnal period of at least about 9 hours, such that melatonin release occurs according to a profile which, taking into account the existing nocturnal profile, simulates a normal human endogenous melatonin nocturnal profile in plasma, in that administration of the formulation at the beginning of said at least about 9 hour single nocturnal period causes melatonin to be detectable in the plasma in an amount which increases to a peak in the course of said period and subsequently decreases to a post-peak minimum essentially at the end of said period.

    CircadinMarket authorization in Europe was granted in 2007 for Neurim's product (Circadin), 15 years after Neurim filed its patent application thus leaving only five years of term for its patent.

    The Opinion also described the parties submitting written observations and oral argument before the ECJ:  Neurim Pharmaceuticals, the United Kingdom Government, the Portuguese Government, and the European Commission.  The Commission and Neurim argued that Article 3d does not preclude grant of an SPC on a "medicinal product comprising an active ingredient where an earlier marketing authorisation (A) has been granted which is for a different medicinal product comprising that active ingredient" (with the caveat that the "limits of the protection" from the "basic patent" would not "extend to the medicinal product the subject of the earlier marketing authorization" and all other requirements of Article 3 are met).  The UK and Portuguese governments took the position that a "second" SPC should not be granted on a medicinal product where the active ingredient had previously been the subject of an SPC.

    Advocate General Trstenjak addressed the first question by considering a "literal interpretation" of the language of the regulation, and then assessing the result to determine whether it is consistent with "the schemes and objectives" of the SPC regulations to come to her conclusion as to the first Question Presented.  In this analysis, the AG determined that the literal meaning of the words of the regulation would preclude grant of a subsequent SPC where a previous SPC had been granted on a medicinal product containing the same active ingredient.  However, the AG then determined that such a result would be contrary to the "schemes and objectives" of the regulation.  Specifically, the AG noted that is was certainly the case that the same active ingredient could be the subject of patent protection for different formulations and uses, as was the case here:  Neurim had a patent for its Circadin insomnia forumation and Hoechst had a patent for its Regulin product for use in sheep breeding (which had expired in 2007).  As a consequence, the AG's Opinion states that "[i]t must therefore be assumed that, in principle, Article 3(a) permits the grant of more than one supplementary protection certificate for a product."  The AG reached the same conclusion with regard to Article 3(b), because that Article provides for market approval for, inter alia, human and veterinary uses.  The AG's Opinion thus concludes that "Article 3(b) also permits, in principle, multiple supplementary protection certificates for products which are used as active ingredients in different medicinal products."  While Article 3(c) by its plain wording would seem to preclude grant of a subsequent SPC on an active ingredient that had received a prior SPC, the AG concluded that "requirement may not be construed as meaning that only one supplementary protection certificate could be granted for a patented active ingredient or for a patented combination of active ingredients" in view of the ECJ's case law.  Because there is thus a "common feature" of Articles 3(a), (b) and (c), the AG concluded that "the schematic context" of Article 3(d) also suggests that this Article would also permit grant of more than one SPC.

    The AG then discussed "teleological" considerations, that is, directed at a consideration of the purpose of the SPC regulations.  Here, the AG noted that "the aim of granting supplementary protection certificates for medicinal products is essentially to extend the term of patent protection for active ingredients used in medicinal products."  Recognizing that protracted regulatory approval proceedings can seriously reduce the patent term remaining when regulatory approval is finally achieved.  The AG appreciates the "view of the European Union legislature" to be that SPCs are needed and granted to remedy the insufficiencies in patent protection occasioned by these long delays in regulatory approval.  Thus:

    Those rules [i.e., the SPC Regulations] are intended to achieve a balance between the various interests at stake in the pharmaceutical sector.  Those interests include, on the one hand, the interests of the undertakings and institutions, some of which pursue very cost-intensive research in the pharmaceutical sector and therefore favour an extension of the term of protection for their inventions in order to be able to balance out the investment costs.  On the other hand, there are the interests of the producers of generic medicines who, as a consequence of the extension of the term of protection of the active ingredients under patent protection, are precluded from producing and marketing generic medicines.  It is also relevant in this connection that, in general, the marketing of generic medicinal products has the effect of lowering the prices of the relevant medicinal products.  Against that background, the interests of patients lie between the interests of the undertakings and institutions conducting research and those of the producers of generic medicines.  That is because patients have an interest, on the one hand, in the development of new active ingredients for medicinal products, but, on the other, they also have an interest in those products then being offered for sale as cheaply as possible.  The same applies to State health systems in general which, in addition, have a particular interest in preventing old active ingredients from being brought onto the market in slightly modified form under the protection of certificates but without genuine innovation and thereby artificially driving up expenditure in the health sector.

    Applying these factors to the case before the Court, the AG recommended that the "absolute preclusive effect" resulting from a prohibition of a subsequent SPC to Neurim for its Circadin product "would be not compatible with the objectives of [the SPC] Regulation[]."  Conversely, granting an SPC under these circumstances is consistent with Article 54(5) of the European Patent Convention (EPC), which "expressly recognises the patentability of 'second and further medical uses' of substances whose use in other medical processes already forms part of the state of the art."  In the AG's view, "it would therefore be contrary to the aims of Regulation No 1768/92 if, in a case like the main proceedings, an application for a supplementary protection certificate would inevitably be unsuccessful because the patented active ingredient has already been placed on the market in another medicinal product."  The AG emphasizes that the prohibitions of Article 3(c) remain, that "prohibit the grant of more than one certificate for each basic patent" (emphasis in original).

    The AG then recognized that while her Opinion is consistent with one line of cases in the ECJ (including Medeva, Georgetown Unversity and Others, and AHP Maufacturing), it is inconsistent with other cases where the ECJ has interpreted the law more stringently.  These cases include Synthon, and Generics (UK), but the AG appears to believe that the Opinion is more consistent with the "first line" of ECJ cases and thus is a sound legal representation.

    The AG rendered a recommendation on Questions 2 through 5 more summarily, stating that the term of the SPC for the subsequent approved use is to be made using the same rubrics and limitations as any other SPC.  Question No. 3 the AG answered in the negative, because the "crucial question" is that the product seeking a subsequent SPC does not fall under the scope of any "basic patent" for which a previous SPC was awarded.  Similarly, the fourth and fifth questions were not deemed particularly relevant in view of the AG's recommendations on the first three Questions.

    The AG thus concluded that:

    [A] supplementary protection certificate for a product which is protected by a basic patent in force may be granted only on the basis of the first authorisation which permits that product to be placed on the market as a medicinal product which is within the scope of protection conferred by the basic patent in the Member State for which the application is made.  The fact that the same product has previously been authorised as a medicinal product for human use or a veterinary medicinal product in the Member State for which the application is made does not preclude the grant of a supplementary protection certificate based on a later authorisation to place that product on the market as a new medicinal product, provided the first-authorised medicinal product is not within the scope of protection conferred by the patent designated by the applicant as the basic patent.

    The ECJ's decision to follow the AG's recommendation, while coming as no surprise, certainly changes the landscape for the better for pharmaceutical patents and products in Europe.  It is frequently the case that new uses can be found for old, well-established and characterized drug compounds, and extending the benefit of SPC protection can be expected to shift the investment scales to encourage such new uses.  In a world where the drug pipeline from traditional pharmaceutical companies has dwindled, these considerations may prove crucial to addressing previously unmet medical needs.

  • By Donald Zuhn

    USPTO SealLast week, the U.S. Patent and Trademark Office published its final rule to implement the preissuance submissions by third parties provision of the Leahy-Smith America Invents Act (77 Fed. Reg. 42150).  The final rule concerning preissuance submissions is the first of many final rule notices that the Office is expected to publish in order to implement AIA provisions that, like the preissuance submissions provision, will take effect on September 16, 2012.

    As we noted when the Office published its notice of proposed rulemaking on the preissuance submissions provision in January, § 8 of the AIA amended 35 U.S.C. 122 by adding 35 U.S.C. 122(e), which lists certain conditions that apply to a third-party preissuance submission to the Office in a patent application (see "USPTO Proposes Rules Changes for Implementing AIA Provisions — Preissuance Submissions Provision").  In particular, AIA § 8 permits any third party to submit for the Office's consideration and inclusion in an application's file "any patent, published patent application, or other printed publication of potential relevance to the examination of the application," provided that the submission is made:

    before the earlier of —

    (A) the date a notice of allowance under section 151 is given or mailed in the application for patent; or

    (B) the later of —

    (i) 6 months after the date on which the application for patent is first published under section 122 by the Office, or

    (ii) the date of the first rejection under section 132 of any claim by the examiner during the examination of the application for patent.

    The submission must also "set forth a concise description of the asserted relevance of each submitted document."  This provision of the AIA, which takes effect on September 16, 2012, applies to any patent application filed before, on, or after that effective date.

    The final rule specifies the requirements for a preissuance submission, which must be timely filed (as described above), be in writing, and contain:

    (1) a list identifying the items being submitted;

    (2) a concise description of the relevance of each item listed;

    (3) a legible copy of each non-U.S. patent document listed;

    (4) an English language translation of any non-English language item listed;

    (5) a statement by the party making the submission that the submission complies with the statute and the rule; and

    (6) the required fee.

    The final rule notes that the statutory time period for making a third-party submission will not be tolled by an initial non-compliant submission.  In addition, the Office will not set a time period for a third party to file a corrected third-party submission or accept amendments to a non-compliant submission that was previously filed.  Moreover, the Office will not refund the required fee in the event that a third-party submission is determined to be noncompliant.  With respect to the required fee, the final rule notes that the fee set forth in 37 C.F.R. § 1.17(p), which is currently $180, will apply to third-party submissions containing up to ten documents.  For every ten additional documents, submitters will have to pay an additional fee under § 1.17(p).  The Office will provide an exemption from the fee requirement for third-party submissions listing three or fewer documents, when the submission is the first third-party submission by a third party (or a party in privity with the third party) in a given application.

    The final rule also cautions that third parties must use the dedicated Web-based interface for preissuance submissions when electronically filing such submissions.  This can be done by selecting the "Third-Party Preissuance Submission under 37 CFR 1.290" option on the EFS-Web.

    With respect to the impact of preissuance submissions on applicants (other than the consideration of relevant art during prosecution of a given application), the final rule notes that third-party submissions will not create a requirement on the part of the applicant to independently file submitted documents with the Office in an Information Disclosure Statement.

    In addition to setting forth rules for implementing the preissuance submission provision of the AIA, the final rule also eliminates 37 C.F.R. § 1.99 ("Third-party submission in published application"), which permitted a third party to submit patents or publications relevant to a pending published application and have such submissions entered in the application file, but did not permit the third party to submit an accompanying concise description of the relevance of each submitted document, and limited the time period for such submissions to two months after the date of the patent application publication or the mailing of a notice of allowance, whichever was earlier.  The final rule also eliminates 37 C.F.R. § 1.292, which provided for public use proceedings.  The Office noted in the final rule notice that such proceedings were no longer necessary in view of post-grant review proceedings, provided by § 6 of the AIA, in which prior public use may be raised.

    The Office made several changes to the proposed rules on preissuance submissions in response to comments received following publication of the Office's notice of proposed rulemaking.  Among the changes are the following:

    • The Office had proposed allowing third-party submissions in reissue applications, but in view of public comments it received decided not to adopt its previously proposed position.  The final rule notice explains that because a reissue application is a post-issuance proceeding, a preissuance submission should not be permitted in a reissue application.  The Office recommended that third parties seeking to submit information in a reissue application should use the protest provisions of 37 C.F.R. § 1.291 instead.

    • The Office had also proposed amendments to § 1.291 to make the requirements for submitting protests clearer and more consistent with the requirements for submitting preissuance submissions under new § 1.290, but in view of comments it received decided to limit its efforts to harmonize § 1.290 and § 1.291.  The final rule notice explains that the Office's proposed attempt to harmonize these sections may have resulted in some confusion.

    • As a result of numerous comments it received regarding third party notification, the Office has decided that it will notify a third party of a non-compliant submission and inform the submitter of the reasons for non-compliance, provided that the third party provides an e-mail address with its submission (whether filed electronically or on paper).

    • As a result of numerous comments it received regarding applicant notification, the Office has also decided that it will notify applicants upon entry of a compliant third-party submission, provided that the applicant participates in the e-Office Action program.

  • By Kevin E. Noonan

    Washington - Capitol #5Companion bills were introduced in Congress on April 25th of this year with little fanfare (particularly in comparison to the Leahy-Smith American Invents Act) but they have the potential to provide significant funding for university-related start-up companies.  The bills, H.R. 4720 and S. 2369, are entitled the "America Innovates Act of 2012" and are sponsored by Reps. Rush Holt (D-NJ) and Timothy Bishop (D-NY) in the House of Representatives and Sens. Frank Lautenberg, Sherrod Brown (D-OH), and Kirsten Gillibrand (D-NY) in the Senate.  They have been referred to their respective committees (the House Sub-Committee on Technology and Innovation and the Senate Committee on Commerce, Science, and Transportation), but to be frank it is unlikely that they will receive positive action in this election year.

    The bill provides for the U.S. to establish an American Innovation Bank as an "independent agency," (Sec. 101(a)) that will "promote the commercialization of science and engineering discoveries" (Sec. 102(a)) by "provid[ing] grants, loans, and other assistance to eligible entities and individuals to enable the entities and individuals to perform the necessary research and development to make research discoveries attractive for private investment that will lead to the development of new companies, products, and jobs." Sec. 102(b).  There are provisions for a Board (Sec. 101(b)(1)) and a Director, appointed by the President with the advice and consent of the Senate (Sec. 101(B)(2)); the Board will "advise the Director on new and emerging areas of research and industry that would benefit from investment from the Bank" (Sec. 101(b)(3)(A)) and "critically evaluate the success of the Bank's investments in helping to commercialize scientific discoveries and create new companies and jobs." (Sec. 101(B)(3)(B))  The bill also provides for annual Reports of its activities to Congress (Sec. 103(a)) that will include at a minimum the number of patents, products, new companies and jobs resulting from Bank investments (Sec. 103(b)).

    Grants will be available to "eligible entities" (Sec. 104(a)) that will include "institutes of higher education" as defined by section 101 of the Higher Education Act of 1965 (20 USC 101), Sec. 104(B)(1) and "nonprofit research institution[s] that focus[] on science research" (Sec. 104(B)(2)).  The grants will be awarded "on a competitive basis" (Sec. 104(d)) in life sciences, medicine, computer sciences, communications, technology, physical sciences, engineering and "[o]ther research areas determined important for economic development by the Director" (Sec. 104(d)(1) – (4)) and using a priority system that awards institutions already receiving "a significant amount of Federal funding" from the National Institutes of Health (NIH), National Science Foundation (NSF), Department of Energy (DOE) or "other agencies" (Sec. 104(e)(1)), that "do not have a significant proof of concept fund already established at the entity" (Sec. 104(e)(2)), have "established relationships" with business and industry that can commercialize the technology and "may be" local industries (Sec. 104(e)(3)), that have "an institutional environment that is supportive of business development" (Sec. 104(e)(4)(A) & (B)) and "demonstrate the appropriate administrative capacity" to encourage patenting, companies, products or jobs from the grants (Sec. 104(e)(5)).  Decisions on grants will be made by an advisory panel of experts, both business leaders and scientists, who will make recommendations to the Director based on grant applications submitted by prospective awardees (Sec 104(c)).  Funds may be used to support the scientists performing the research as well as further research or data collection directed to making a discovery "more attractive" to corporations or venture capital firms (Sec. 104(f)(1)(A)), for facilities and business incubators (Sec. 104(f)(1)(C))  and to attract additional private investment (Sec. 104(f)(1)(D)).  The bill also contains additional provisions governing subgrants to individuals (Sec. 104(f)(2)) and for facilities construction (Sec. 104(f)(3)).  And of course there are provisions for Reports from grantees for each year during the grant period as well as for 5 years after the grant period ends (Sec. 104(g)).

    In addition, the bill provides for direct grants to individuals (Sec. 105), governed by many of the same considerations and requirements for institutional grants (Sec. 105(a) – (c)), as well as grants to private companies in the form of loans "at competitive interest rates" (Sec. 106).  But when the government giveth it can also taketh away, under conditions where the grantees "do not use such grants or loans to make reasonable attempts to develop discoveries into new companies, products, or jobs" and can require repayment, as provided by Sec. 107.

    Section 201 et seq. sets forth provisions for "improving science and technology" by amending Section 510 of the NSF Authorization Act of 2010 (42 USC 1869) to permit the NSF to award grants under the Integrative Graduate Education and Research Traineeship (IGERT) program to support students who perform "some or all of their graduate research in an industry setting." (Sec. 201).  In addition, the bill provides that NSF, NIH or any other Federally funded graduate student training program must provide students with training related to protecting intellectual property, commercializing inventions and developing scientific discoveries (Sec. 202(a)-(b)), exempting institutions of higher education that enroll fewer than 6 students (Sec. 202(c)).  The NSF Authorization Act is further amended to award grants for "professional science masters programs" (Sec. 301).

    The Bank is intended, among other things, to help companies navigate the "valley of death" where university-related start-up companies go through initial funding monies before having sufficient experimental results to attract venture capital or large company investment or commercialize their products.  One of the bills' proponents, Senator Gillibrand, called the bill "common-sense legislation [that] will help develop scientific breakthroughs into cutting-edge businesses and new jobs."  That kind of promotion worked well for the AIA, and could be the ticket for accelerating consideration of the bills before November.

  • By Kevin E. Noonan

    MyriadThe Federal Circuit heard oral argument in Association for Molecular Pathology v. U.S. Patent and Trademark Office (the Myriad case) on Friday, and the cast of characters remained mostly the same.  On the panel were Judge Lourie, Judge Bryson, and Judge Moore.  Representing Myriad was Gregory Castanias from Jones Day, and Chris Hansen reprised his role as ACLU/AMP advocate.  New to the proceedings was Melissa Patterson for the U.S. government, in place of former Acting Solicitor General Eric Katyal who has left the government for private practice.  Each side had a nominal twenty minutes to argue, with Mr. Hansen conceding half his time to Ms. Patterson.

    Castanias, GregoryMr. Castanias (at left) began his argument as he would end it, citing Diamond v. Chakrabarty as the seminal authority on the patent-eligibility of product claims and stating that the Supreme Court's decision in Mayo v Prometheus did not change this.  Taking the argumentative bull by the horns, he addressed the issue of "preemption" (which would be a theme in both Mr. Hansen's and Ms. Patterson's arguments) by saying that preemption is a proxy for whether there is an invention.  Judge Lourie posed the contrast between a law of nature (in Mayo) and an isolated natural material (here) in instances where there was only a "small move" from the naturally occurring molecule.  Mr. Castanias answered in a manner that would raise philosophical issues for Myriad later, citing to the expert declarations by the inventors and others on the question of how small the step actually was.  Here, his point was that there was a great deal of human ingenuity involved in producing the isolated genomic DNA encompassed by the claims, and that contributes to its inventiveness.

    Mr. Castanias then reminded the Court of Judge Bryson's analogy regarding making a baseball bat from wood (and the judge included sculpting a statue of David from marble), which were patent-eligible, and Judge Bryson then asked about whether isolating genomic DNA was like cutting off the branches and roots of a tree and then claiming a trunk (illustrating again that bad analogies make bad law), with the wrinkle that the trunk was produced using a laser that caused chemical changes.  Mr. Castanias agreed that this would not be patent-eligible but because it is not an invention, being just a new way to make an old thing.  With a gene, he emphasized that it is unknown until an inventor identifies, and in some sense, defines it.  Citing the '282 patent, he pointed to Figure 10 and to columns 19 and 24 of the specification, for the teaching that what the patent defines as a "gene" includes the coding sequences, the intervening sequences (or "introns" to the coding sequences "exons") and regulatory sequences that could themselves encompass 100 kilobases (100,000) of DNA.  The inventors defined this as the BRCA1 gene, which required an enormous amount of inventive effort, according to Mr. Castanias (making it very unlike a tree trunk).  Judge Lourie leant a hand by remarking that the gene is thus "the product of human ingenuity."

    Judge Lourie then did Myriad and Mr. Castanias no favors by broaching the issue of claim 20 of the '282 patent and asking him to distinguish this claim from the patent-ineligible claims in Mayo.  Mr. Castanias started well, pointing out that, unlike in Mayo, this claim does not encompass the "principle of the holy trinity of well-understood, routine and conventional," as in Mayo, but with something that is not well-understood, routine or conventional, namely the transformed cell.

    But then Mr. Castanias and the bench spent what everyone recognized was a few unfruitful minutes discussing whether claim 20 was properly before the Court.  Mr. Castanias repeated Myriad's contention from its brief, that AMP not only had not included this claim in its certiorari petition but had affirmatively stated that the method claims were not being appealed.  Judge Bryson said that was not the point, and that he (and presumably his colleagues) believed that the Court's "task" was not limited by plaintiffs' certiorari petition (his argument having a strong flavor of not letting the inmates run the asylum).  Judge Bryson characterized the current state of the case as a "do-over" where "the vacated judgment is in the same position as it was last year."  He then asked for any authority for Myriad's position and Mr. Castanias was unable to provide any (Mr. Hansen, during his argument, was happy to provide the Court with Lockheed Martin Corp. v. Space Systems/Loral, Inc. for authority to the contrary).

    Judge Bryson also voiced confusion over the meaning of certain claim language, illustrating again the unusual posture of the case where the claims have never been construed.  Mr. Castanias and the Court were unable to parse out the language "causing cancer" in the phrase "growing a transformed eukaryotic host cell containing an altered BRCA1 gene causing cancer in the presence of a compound suspected of being a cancer therapeutic," which is not surprising:  the claim is not clearly written, and the word "transform" has two meanings in the art easily conflated.  First, a "transformed" cell can mean a cell into which an exogenous DNA has been introduced (most likely the meaning intended in the claim), but it can also mean a cell that has been "oncogenically" transformed to be, inter alia, immortalized so that cell lines can grow indefinitely in vitro.  Again, Mr. Hansen came to the rescue, stating properly that his interpretation of the claim was that the BRCA gene in a form associated with cancer in vivo.  And Judge Moore chimed in asking whether claim 20 comprising the transformed cell would be patent-eligible if the panel found the isolated DNA claims not to be patent-eligible.  For her, "transformation" (unclear whether in the biological or legal sense) was irrelevant.

    Hansen, ChristopherMr. Hansen (at right) began his argument by noting what he called the "stunning breadth" of the composition of matter claims, and the "preemptive effect" of such claims, but Judge Lourie interrupted by noting that breadth is properly a concern under Section 112 and not Section 101 of the Patent Act.  Mr. Hansen proceeded to read the laundry list of types of nucleic acids recited in the '282 specification, but Judge Lourie again interrupted and asked about the relevance of this to the issues raised in Mayo.  In response to Judge Lourie's assertion that the "law of nature" argument in Mayo was not directly relevant to composition claims, Mr. Hansen asserted a "law of nature"/"product of nature" exclusion (the latter being completely fantastical as far as actual case law is concerned), saying that these should be "available to everyone" under Supreme Court precedent.  Judge Moore noted that his breadth argument undercut his preemption argument, because if preemption the issue, breadth is irrelevant under Mayo.  She indicated that preemption is a "bright line prohibition" and thus this argument is "a waste of time and space."

    Wisely, Mr. Hansen took the opportunity to move on to claim 20.  In this argument he produced the wildest of wild hair arguments (which is saying something in this case), asserting that Myriad "bought the transformed cell off the shelf" and that "it wasn't their invention."  (Reality check:  it would have been impossible to produce a recombinant (or "transformed") cell comprising a cancer-causing BRCA gene variant until such a gene was isolated by Myriad.)  Judge Lourie pointed out that in Mayo the claims recited administering and determining and the Supreme Court demanded something more, significantly more, asking whether that was not provided in claim 20 (presumably, the transformed cell).  Mr. Hansen was able to argue it did not, because having falsely negated the inventiveness of the BRCA transformed cell he could concentrate on the rest of the claim, which recited "[growing said transformed eukaryotic host cell] in the presence of a compound suspected of being a cancer therapeutic, growing said transformed eukaryotic host cell in the absence of said compound, determining the rate of growth of said host cell in the presence of said compound and the rate of growth of said host cell in the absence of said compound and comparing the growth rate of said host cells."  Then the claim directs the practitioner to "see what happens," and moreover, with anything — "salt, sugar, water, oil" as opposed to the non-naturally occurring drug in Mayo — and without any recitation of the type of "precise numbers" the Supreme Court rejected in Mayo.  Judge Moore pointed out that the transformed cell is not found in nature and asked how this differs from Chakrabarty's bacterium.  Mr. Hansen merely reminded the Court that the drug in Mayo had not been found in nature.  Judge Lourie then raised the example of Penicillin G, which was a natural product and asked whether it should be patent-eligible.  Mr. Hansen stated that it depended on "the degree to which it is transformed" (presumably from its natural state) but said that the rule has to be that it doesn't matter for method claims — "administering and looking to see what happens is not patentable."  Judge Lourie sounded skeptical of this reasoning, mentioning that Penicillin G was not patented and there was "a lag" between when it was discovered by Fleming and when it was commercially available.

    Mr. Hansen then said that it is well-accepted that patents are not rewarded for being the product of great effort, saying that E=mc2 might have taken great effort but was not patent eligible.  Judge Bryson said that wasn't his understanding of AMP's argument and returned the questioning back to claim 20, asking if Mr. Hansen agreed that "if all you did was to put PenG next to bacterium and tested and it worked better than water, then that isn't patentable," which, of course, he did.

    Department of Justice (DOJ) SealLast to speak was the government, represented by Melissa Patterson.  Her argument proved that, although former Acting Solicitor General Katyal may be gone, his arguments (and his magic microscope) remain.  Ms. Patterson started as Mr. Hansen did, with an argument regarding the "unduly preemptive" scope of Myriad's composition of matter claims.  Judge Moore raised the magic microscope, asking whether the government still thought that was a useful test.  Ms. Patterson, with the benefit of hindsight characterized it as a metaphor rather than a test, but stated that the government still considered it "useful" as such.  The government's position was that the Supreme Court had voiced a "concern" in Mayo regarding the extent to which claims preclude public access to a product of nature; in this version of the government's view, the preemption issues raised for process claims in Mayo are directly applicable to the preemptive issues the government — and, coincidentally, the ACLU — raise here.  Judge Bryson raised the issue of whether the views of the U.S. government included the views of the Commerce Department and the USPTO, and Mr. Patterson stuck to the "unitary Executive" stance espoused (to some skepticism from Judge Moore) in the previous oral argument in this case.

    Turning back to the merits, Ms. Patterson stated that the government did not consider this a "close case," analogizing (badly) Myriad's claims to patenting an electron or a quark (or a Higgs boson, noted Judge Lourie).  She then said that the government did not believe there should be a "huge wall" between the law of nature and product of nature and that the government was seeking to assert a general rule not a rule specific for DNA.  She went on to say that changes in a product of nature "incidental to its extraction" raised preemption concerns, citing coal as an example.

    Judge Moore raised the issue of "settled expectations" as she had at the previous oral argument, noting that an industry had arisen during the "decades" in which the government (through the USPTO) had granted these patents.  Ms. Patterson raised Bilski as an example of where "thousands" of patents had been invalidated and said that the "settled expectations" provided "no reason to alter how a court looks at Section 101," asking the Court to make general (and preclusive) rules on patent eligibility.

    Ms. Patterson then turned to a more potentially pernicious portion of her argument, saying that products of nature that differ "only by changes that are incidental to extraction" too broadly preempt the public's ability to study and otherwise use them.  Judge Moore raised the issue of primers and probes, which Ms. Patterson dismissed as "depend[ing] on the inherent properties of basepair complementarity" (thus presumably relegating anything that occurs naturally to be patent-ineligible so long as it continues to evince "inherent properties").  Judge Moore continued, asking about Chakrabarty's bacterium and the Court's rubric of things being "distinct and markedly different," to which Ms. Patterson returned to coal and uranium — as properties discovered but not "invented."

    In his rebuttal time, Mr. Castanias clarified the language of claim 20 and disputed Mr. Hansen's allegations that the transformed cell was something Myriad "got of the shelf, like a test tube."  He also attacked the government's argument as establishing "no principled line" for making the distinction between patent eligibility and ineligibility, and said that Chakrabarty draws the line.  He also distinguished his earlier remarks as not being a "sweat of the brow analysis" for patent eligibility but being the product of "work and inventive judgment."

    Judge Moore asked Mr. Castanias to distinguish isolating a gene from extracting coal from rock, which he admitted would not be patent eligible, and mentioned the additional utilities present in an isolated gene, including re-introducing the gene into a cell that had a defective copy.  Utility had not been litigated in this case, he reminded the Court, the plaintiffs' having conceded that the isolated DNA had utility.

    Judge Bryson returned to his kidney hypothetical from the previous oral argument, and Mr. Castanias attempted to distinguish without much success.  Judge Lourie ended this line of questioning by reminding the panel that a kidney is an organ, not a chemical compound, and that the analogy breaks down when that is taken into account.

    Mr. Castanias ended his rebuttal argument by rebutting a point persuasive to Judge Bryson in his dissent from the now-vacated decision:  that "whole genome sequencing" was not impacted by Myriad's isolated DNA claims.  He mentioned that Professor Watson had had his whole genome sequenced without infringement liability.  After some additional questions regarding the importance of "where to make the cut" (and some colloquy from Judge Lourie that some of these considerations sound in obviousness, which was not before the Court), Mr. Castanias ended with his most persuasive argument:  that Chakrabarty is the answer and Mayo doesn't change it.

    One thing is clear from this argument.  The danger in AMP's preemption argument, and even more so in the government's argument, is something hinted at in the now-vacated Federal Circuit majority opinion.  That is the argument, expressed frankly by the government, that merely isolating something from nature was "not enough" to render it patent eligible.  Part of the problem is the government's avowed purpose for setting out "general rules" (one shudders to think of the implications for "bright line" rules made by people who don't understand the implications).  Another is the failure to discuss the inseparable impact on what is claimed and how it is claimed.  Using one of the examples raised with regard to claim 20, what of the patent-eligibility of penicillin?  That question varies with the nature of the claim:

    1.  Penicillin.

    2.  An isolated preparation of penicillin having a purity of greater than 99% and capable of killing one million bacterial cells per microgram.

    3.  A pharmaceutical preparation of penicillin suitable for injecting into a human being to treat a bacterial infection.

    Philosophically (while we are talking general principles), the government's position that claims should not be allowed that will preempt a "product of nature" is a good way to create a "tragedy of the commons," because there is no incentive to identify, isolate/extract, test, and produce a drug from a naturally occurring source if its source precludes patent eligibility.

    What the government (or that portion of the government populated by the scientifically illiterate or their opposites, the scientific elite who have little appreciation for the legal and practical implications of their positions) does not recognize is that there is a good reason to make the distinction between natural law as in Mayo (even as marginally as the logic of that case is laid out) and isolated products from nature.  Patenting a natural law restricts development of any future application of that law during the lifetime of the patent, whereas patenting a chemical compound from nature is limited to that compound.  Indeed, it has always been the case that "the public" is free to find new uses for compounds made by others and to patent them, which the original product patentee cannot practice without a license.  Thus, product patents by their nature do not have the breadth of method patent claims and do not raise the same issues due to the specificity of what is claimed in a composition of matter claim.  That distinction renders much of what the government argues as irrelevant, or at least not tethered to any legitimate policy concern regarding the availability of "products of nature" to the "public."

    No matter how the Federal Circuit decides this case, what is at stake is a larger principle.  The old aphorism (raised to an anthem by John Cougar Mellancamp) is that if you don't stand for something, you fall for anything.  What the Court needs to stand for is the Congressional intent that "anything under the sun made by man" is eligible for patenting.  If the Supreme Court indulges in judicial nullification of this intent, so be it (and even the Court recognizes that Congress can amend the law to overcome all but the most fundamental grounds for patent ineligibility).  But the Federal Circuit spent a generation under the leadership of Judge Rich, and Judge Markey, and all the other Chiefs and other judges, in fulfilling its mandate of being the court that understands technology and patent law and thus is in the best position to interpret that law and apply it to the cases before it.  It should continue to do so.

  • By Donald Zuhn

    NVCALast week, the National Venture Capital Association (NVCA), a trade association representing the U.S. venture capital industry, released the results of its MoneyTree Report on venture funding for the second quarter of 2012.  The report, which is prepared by NVCA and PriceWaterhouseCoopers LLP using data from Thomson Reuters, indicates that venture capitalists invested $7.0 billion in 898 deals in the second quarter, which constituted a 17% increase in dollars and a 11% decrease in deals as compared with the first quarter of 2012, when $6.0 billion was invested in 809 deals.  The NVCA also revised its first quarter numbers, raising the funding and deals totals by $200 million and 51, respectively.  As a result, the first quarter drop was somewhat less severe than initially reported (see "Biotech Venture Funding Drops 43% in First Quarter").

    Venture Funding 2012-Q2
    The report also notes that the Life Sciences sector (biotechnology and medical device industries) saw another decrease in both dollars and deals in the second quarter, dropping by 9% in funding to $1.4 billion and by 6% in deals to 174.  The drop in Life Sciences funding was the industry's fourth consecutive quarterly decrease, and was due mostly to a drop in Biotech funding where $697 million went into 90 deals, down from the $780 million that was invested in 99 deals in the first quarter.  Medical device funding remained flat with respect to dollars ($700 million) and was up 11% with respect to deals (84).  In contrast with the Life Sciences sector, the Software industry received the highest level of funding, securing $2.3 billion in the second quarter — which marked a 38% increase over the first quarter.  The Software industry also led all sectors in deals with 290, a 16% increase over the first quarter.  Overall, eleven of the seventeen sectors tracked by the NVCA saw increases in dollars invested in the second quarter (in the first quarter, the numbers were flipped with eleven of seventeen sectors seeing decreases).  Eleven of seventeen sectors also saw increases in the number of deals being completed.

    PricewaterhouseCoopers (PWC)NVCA president Mark Heesen noted that "[t]he concentration of venture capital dollars in the hands of fewer firms will increasingly dictate the flow of investment," adding that this currently "translates into more funding for IT start-ups and less capital available for life sciences and clean technology."  He also noted that the NVCA "hope[s] to see this investment mix rebalance over time as the start-up ecosystem is better served with more diversity, not less."  Tracy Lefteroff, the global managing partner of the venture capital practice at PricewaterhouseCoopers pointed out that at the current pace venture funding in 2012 was unlikely to outpace the 2011 total of $30 billion, but would still exceed the 2010 total of $23 billion.  She also noted that "Software and Internet companies continue to be attractive industries for VCs since most of these companies tend to be capital efficient and don't require large amounts of capital to operate," and that "given the regulatory challenges currently impacting the Life Sciences industry and the amount of capital required to fund these companies, it's no surprise that investments in this industry have declined for the fourth consecutive quarter."

    For additional information regarding this and other related topics, please see:

    • "Biotech Venture Funding Drops 43% in First Quarter," May 3, 2012
    • "Venture Funding Increased 22% in 2011," February 2, 2012
    • "Life Sciences Venture Funding Drops in Third Quarter," October 27, 2011
    • "Life Sciences Venture Funding up 37% in Second Quarter," August 1, 2011
    • "VentureSource Reports 35% Increase in 1Q Venture Funding," April 26, 2011
    • "NVCA Reports Modest Gains in First Quarter Venture Funding," April 19, 2011

    • "NVCA Reports 31% Drop in Venture Funding for Third Quarter," October 17, 2010

    • "NVCA Reports 34% Increase in Venture Funding for Second Quarter," July 22, 2010

    • "NVCA Report Shows First Quarter Drop in Venture Funding," April 20, 2010

    • "Biotech/Pharma Financing Improving, R&D Spending Up," August 31, 2009
    • "NVCA Study Shows Increase in Third Quarter Venture Funding," October 23, 2009

    • "First Quarter Venture Capital Funding at 12-Year Low," April 23, 2009

    • "NVCA Study Shows Decline in 2008 Investment; BIO Study Predicts Biotech Rebound in 2009," February 16, 2009

    • "NVCA Predicts Another Slow Year for Venture-backed Businesses in 2009," December 18, 2008

  • By Sherri Oslick

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

    Novartis Pharmaceuticals Corp. et al. v. Sun Pharmaceuticals Industries, Inc. et al.
    2:12-cv-04393; filed July 14, 2012 in the District Court of New Jersey

    • Plaintiffs:  Novartis Pharmaceuticals Corp.; Novartis Corp.; Novartis AG
    • Defendants:  Sun Pharmaceuticals Industries, Inc.; Sun Pharma Global FZE; Caraco Pharmaceutical Laboratories, Ltd; Sun Pharmaceutical Industries Ltd.

    Infringement of U.S. Patent No. 7,932,241 ("Pharmaceutical Products Comprising Bisphosphonates," issued April 26, 2011) following Paragraph IV certifications as part of Sun's filing of ANDAs to manufacture generic versions of Novartis' Reclast® (zoledronic acid injection, once-yearly treatment for postmenopausal osteoporosis) and Zometa® (zoledronic acid injection, used to treat patients with multiple myeloma and patients with documented bone metastases from solid tumors).  View the complaint here.


    Shionogi Inc. et al. v. Nostrum Laboratories, Inc. et al.

    1:12-cv-04402; filed July 13, 2012 in the District Court of New Jersey

    • Plaintiffs:  Shionogi Inc.; Andrx Corp.; Andrx Pharmaceuticals, Inc. a/k/a Watson Laboratories, Inc.- Florida; Andrx Pharmaceuticals, L.L.C.; Andrx Laboratories (NJ), Inc.; Andrx EU Ltd.; Andrx Labs, L.L.C.
    • Defendants:  Nostrum Laboratories, Inc.; Nostrum Pharmaceuticals LLC

    Infringement of U.S. Patent Nos. 6,099,859 ("Controlled Release Oral Tablet Having a Unitary Core," issued August 8, 2000) and 6,866,866 ("Controlled Release Metformin Compositions," issued March 15, 2005), both licensed to Shionogi, following a Paragraph IV certification as part of Nostrum's filing of an ANDA to manufacture a generic version of Shionogi's Fortamet® (extended release metformin hydrochloride, used to treat Type 2 diabetes).  View the complaint here.

  • Calendar

    July 30-31, 2012 – Freedom to Operate*** (American Conference Institute) – Philadelphia, PA

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

    August 2, 2012 – USPTO Post-Grant Proceedings:  Meeting the New Requirements for Post-Grant and Inter Partes Reviews and Supplemental Examination (Strafford) – 1:00 – 2:30 pm (EDT)

    September 9-11, 2012 – IPO Annual Meeting (Intellectual Property Owners Association) – San Antonio, TX

    September 10-12, 2012 – Business of Biosimilars & Generic Drugs (Institute for International Research) – Boston, MA

    September 20-21, 2012 – FDA Boot Camp*** (American Conference Institute) – Boston, MA

    September 24-25, 2012 – Biosimilars and Biobetters*** (SMi) – London, UK

    September 25-26, 2012 – EU Pharma Regulatory Law*** (C5) – Brussels, Belgium

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