• CalendarApril 9, 2012 – Mayo v. Prometheus (Law Seminars International) – 2:30 – 3:30 pm (Eastern)

    April 16-18, 2012 – Intellectual Property Counsels Committee (IPCC) Spring Conference & Meeting (Biotechnology Industry Organization) – Austin, TX

    April 17, 2012 – 28th Annual Joint Patent Practice Seminar (Connecticut, New Jersey, New York, and Philadelphia Intellectual Property Law Associations) – New York, NY

    April 18, 2012 – European Biotech Patent Law Update (D Young & Co.) – 7:00 am and 12:00 pm (EDT)

    April 18, 2012 – Patent Term Adjustments and Extensions: Recent Developments (Strafford) – 1:00 – 2:30 pm (EDT)

    April 24, 2012 – Patent Law in Light of Mayo v. Prometheus: Claims to Laws of Nature Are Not Patentable (American Bar Association) – 1:00 – 2:30 pm (EDT)

    April 24-25, 2012 – Paragraph IV Disputes*** (American Conference Institute) – New York, NY

    April 26, 2012 – Moving From First to Invent to First to File: Understanding the Opportunities and Challenges (Technology Transfer Tactics) – 1:00 – 2:00 pm (Eastern)

    May 1, 2012 – Prometheus in the Post-Bilski Age: Patentable Subject Matter Under Continued Attack (Strafford) – 1:00 – 2:30 pm (EDT)

    May 2, 2012 – Patent Prosecution under the AIA: Strategies for Before, During and After the Transition to First-Inventor-to-File (American Intellectual Property Law Association) – 12:30 – 2:00 pm (Eastern)

    May 3, 2012 – In-Depth Analysis of Mayo v. Prometheus: What it Means for the Future of Medical Diagnostic Patents (Technology Transfer Tactics) – 1:00 – 2:00 pm (Eastern)

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

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

  • Technology Transfer Tactics will be offering a webinar providing an "In-Depth Analysis of Mayo v. Prometheus: What it Means for the Future of Medical Diagnostic Patents" on May 3, 2012 from 1:00 – 2:00 pm (Eastern).  Patent Docs author Dr. Kevin E. Noonan of McDonnell Boehnen Hulbert & Berghoff LLP will dissect the Supreme Court's decision, help attendees understand how to adjust patent strategy in light of this development, and guide attendees in drafting future claims.  The webinar will cover the following topics:

    • Review the Supreme Court decision's implications on future Federal Circuit rulings, including Myriad;
    • Provide guidance on the criteria required to establish subject matter patent eligibility;
    • Unveil practical strategies for drafting claims in compliance with the ruling's interpretation; and
    • Discuss what lessons can be learned from the decisions for future patentability challenges.

    The registration fee for the webinar is $197.  Those interested in registering for the webinar, can do so here.

    Technology Transfer Tactics

  • Strafford #1Strafford will be offering a webinar/teleconference entitled "Prometheus in the Post-Bilski Age: Patentable Subject Matter Under Continued Attack" on May 1, 2012 from 1:00 – 2:30 pm (EDT).  Stephen T. Schreiner of Goodwin Procter and Marcus T. Hall of Winston & Strawn will prepare patent counsel to argue patentability under 35 U.S.C. § 101, discuss the impact of recent Federal Circuit and ITC decisions — including the Supreme Court's Prometheus ruling, and offer best practices for patent seekers to meet subject matter eligibility requirements.  The webinar will review the following questions:

    • What criteria are required to establish subject matter eligibility for patents?
    • How have the decisions since Bilski impacted patent eligibility?
    • What lessons can be learned from the decisions for future patentability challenges?
    • What strategies should patent applicants employ to improve the likelihood of a successful patent application?

    An interactive Q&A session will follow the presentation.

    The registration fee for the webinar is $297 ($362 for registration and CLE processing).  Those interested in registering for the webinar, can do so here.

  • ABAThe American Bar Association (ABA) will be offering a teleseminar entitled "Patent Law in Light of Mayo v. Prometheus: Claims to Laws of Nature Are Not Patentable" on April 24, 2012 from 1:00 – 2:30 pm (EDT).  James R. Myers, Ching-Lee Fukuda, and Jane T. Gunnison of Ropes & Gray LLP will examine the Mayo v. Prometheus opinion and will clarify patent eligibility as a subject matter under Section 101 of the Patent Act.

    The registration fee for the webcast is $169 (for either the telephone seminar or audio webcast options).  Those interested in registering for the teleseminar, can do so here, by calling 800-CLE-NEWS (800-253-6397), or by faxing an order form to 215-243-1664.

  • AIPLAThe American Intellectual Property Law Association (AIPLA) will be offering a webinar entitled "Patent Prosecution under the AIA: Strategies for Before, During and After the Transition to First-Inventor-to-File" on May 2, 2012 from 12:30 – 2:00 pm (Eastern).  Joseph D. Matal, Judiciary Committee Counsel to Senator Jon Kyl, will discuss changes in 35 U.S.C. § 102 under the Leahy-Smith America Invents Act, and what constitutes prior art, as well as provide insight on the legislative process that created the AIA, and legislative history that produced the Act.  Courtney Brinckerhoff of Foley & Lardner LLP will discuss how to prepare for the transition to the "first-inventor-to-file" system in the AIA, and provide strategies that patent practitioners and their clients can adopt now, before the act goes into effect.

    The registration fee for the program is $145 (AIPLA member rate) or $175 (non-member rate).  Those interested in registering for the program, can do so here.

  • By Donald Zuhn

    USPTO SealOn Monday, the U.S. Patent and Trademark Office announced that it will be implementing a new After Final Consideration Pilot (AFCP) program, which will allow applicants and examiners to work together in after final situations to move applications toward allowance.  In particular, the AFCP program provides examiners with a limited amount of non-production time to consider responses filed following a final rejection.  For utility, plant, and reissue applications, the limited amount of non-production time will be three hours (design applications will be afforded one hour).  According to the Office's announcement of the new program, "[e]xaminers will be encouraged to use their professional judgment to decide whether a response can be fully considered, including any additional search required, within the time limit in order to determine whether the application is in condition for allowance."

    The Office has created a separate webpage for the new AFCP program, which indicates that the term of the pilot program is currently planned for the third quarter of 2012.  The Office's AFCP webpage also includes a link to notice providing guidelines for the consideration of responses after final rejection under the AFCP program.  The notice indicates that "[o]nce a final rejection that is not premature has been entered in an application, there is no right to unrestricted further prosecution," but "[i]n limited situations further amendments or arguments may be considered."  The notice lists six situations in which a response after final rejection should be entered:

    1.  The amendment places the application in condition for allowance by canceling claims or complying with formal requirement(s) in response to objection(s) made in the final office action.
    2.  The amendment places the application in condition for allowance by rewriting objected-to claims in independent form.
    3.  The amendment places the application in condition for allowance by incorporating limitations from objected-to claims into independent claims, if the new claim can be determined to be allowable with only a limited amount of further consideration or search.
    4.  The amendment can be determined to place the application in condition for allowance with only a limited amount of further search or consideration, even if new claims are added without cancelling a corresponding number of finally rejected claims.
    5.  The amendment can be determined to place the application in condition for allowance by adding new limitation(s) which require only a limited amount of further consideration or search.
    6.  The response comprises a perfected 37 CFR 1.131 or 37 CFR 1.132 affidavit or declaration (i.e. a new declaration which corrects formal defects noted in a prior affidavit or declaration) which can be determined to place the application in condition for allowance with only a limited amount of further search or consideration[.]

    The notice indicates that when an examiner determines that "the nature and extent of the amendments or arguments presented in the response can be fully considered within the limited amount of time authorized by the [AFCP]," the examiner should consider the after final response, and when the examiner determines otherwise, the examiner "should treat the response according to current practice, without non-production time authorized."  The notice also indicates that an allowance is not a required end result for an examiner to be afforded the additional amount of non-production time to consider an after final response.  The notice, however, provides two limitations to the above.  In particular, examiners will not be allotted non-production time in situations 1 and 2 above, because such amendments are normally to be entered under current after final practice, and examiners will get two hours of non-production time if an interview is conducted (examiners will still get three hours of total time, with one hour being credited for the interview).

    The Office notes that it will be assessing the new pilot program to determine whether the additional time for after final consideration of applications will lead to an increase in allowances and a decrease in the number of Requests for Continued Examination that are filed.

  • By Donald Zuhn

    USCLast month, in University of Southern California v. DePuy Spine, Inc., the Federal Circuit vacated and remanded a decision by the Board of Patent Appeals and Interferences awarding priority to Appellee DePuy Spine, Inc. in an interference between DePuy's U.S. Patent No. 6,812,211 and U.S. Patent Application No. 10/230,671.  Appellants University of Southern California and Ampac Biotechnology, Inc. ("USC") filed the '671 application on August 29, 2002, and in 2005, copied claims from the '211 patent into their application.

    The Board declared an interference, defining Count 1 as claim 1 of the '211 patent, which recites:

    1.  A method of treating in a living being an intervertebral disc having a nucleus pulposus, comprising the step of:
        a) injecting a composition consisting essentially of a crosslinking agent into the nucleus pulposus,
        wherein the crosslinking agent is injected in an effective amount to cause in-situ crosslinking of native proteins present in the nucleus pulposus.

    DePuy SpineThe Board originally designated USC as the senior party, according the '671 application the benefit of U.S. Provisional Application No. 60/316,287, which was filed on August 31, 2001 (the '211 patent issued from an application filed on March 19, 2002).  The Board then determined that the specification of the '287 application did not expressly disclose one of the limitations in Count 1, and granted DePuy's motion to deny USC the benefit of the '287 application's filing date.  USC responded by moving to substitute a new count (Count 2) that omitted the undisclosed limitation, but the Board rejected the count as invalid over the prior art.  After finding DePuy's claim 1 to be obvious over the prior art, the Board proposed a new count (Count 3), which it defined as claim 24 of the '671 application.  Claim 24 recites:

    24.  A method of improving the resistance of an intervertebral disc to mechanical degradation by treating in a living being the intervertebral disc having a nucleus pulposus which is degraded or subject to ongoing degradation, comprising the step of:
        a) injecting a composition consisting essentially of a crosslinking agent into the nucleus pulposus,
        wherein the crosslinking agent is injected in an effective amount to cause in-situ crosslinking of native proteins present in the nucleus pulposus.

    In response to the Board's request for comments regarding the proposed count, USC noted that the proposed count retained the undisclosed limitation, and therefore, that it would be prevented from relying on the '287 application as proof of priority.  USC proposed claim 7 of the '671 application as an alternative count.  Claim 7 recites:

    7.  A method of improving the resistance of a collagenous tissue having pyridinoline cross links to mechanical degradation comprising the steps of:
        contacting at least a portion of a load bearing collagenous tissue within a human body with an effective amount of a crosslinking reagent having at least one crosslinking agent under conditions    within physiologic limits to prevent tissue overheating,
        wherein the collagenous tissue is an intervertebral disc.

    The Board rejected USC's request to modify the count as well as USC's request for authorization to file a motion to change the count, and awarded priority to DePuy.

    Federal Circuit SealWhile the Federal Circuit found that the Board did not err in determining that the phrase "in a living being" in the preamble of Count 3 constituted a limitation, the Court vacated the Board's decision awarding priority to DePuy because the Board "adopted a count that prevented USC from relying on its provisional application — which USC argues is its best proof of priority — and repeatedly rejected USC's requests to modify the count."  The Board did so even though it "has recognized that allowing a party to rely on its best proofs of priority 'is an accepted reason in interference practice for granting' a motion to modify the count," citing Grose v. Plank, 15 U.S.P.Q.2d 1338, 1341 (B.P.A.I. 1990).

    The Court noted that the Board failed to "offer any coherent justification for declining to modify the count so USC could rely on its provisional application," and "perplexingly stated that USC 'only suggested a new count in a comment, but never actually moved for the new count,' despite the fact that the Board denied USC authorization to file such a motion."  The Federal Circuit concluded that "[t]he Board erred by insufficiently explaining its decision not to modify Count 3 to allow USC to claim priority to its provisional application," adding that "[t]his failure is particularly troublesome because a party typically should be allowed to rely on its best priority proofs."  In remanding the case back to the Board, the Court stated that USC should be afforded the opportunity to file a motion to change the count, and that "[t]he Board's decision must, at the very least, squarely address the issues USC raises and set out the reasoning supporting the Board’s conclusions in sufficient detail to permit meaningful review."

    University of Southern California v. DePuy Spine, Inc. (Fed. Cir. 2012)
    Nonprecedential disposition
    Panel: Circuit Judges Bryson, Dyk, and Moore
    Opinion by Circuit Judge Moore

  • By Donald Zuhn

    Inovia-2012-US-Global-Patent-IP-Trends-Indicator-1Patent services provider inovia announced the release of its 2012 report on global patent and IP trends today.  In compiling the report, inovia, which produces products for PCT national phase entry, European patent validation, and patent translations, surveyed nearly 150 U.S. companies to identify the trends having the greatest impact on the foreign filing strategies of U.S. patentees.

    The 2012 report notes that 22% of survey respondents are involved in the pharmaceuticals/biotech industry.  Other sectors or groups represented in the survey include chemicals/materials (16%), electrical/electronics (15%), mechanical/engineering (10%), IT/software/media (3%), and university/association/non-profit (22%).  The report also indicates that more than a third of survey respondents (37%) had no in-house patent attorneys or agents, 46% had one to four in-house patent attorneys or agents, and the remainder (17%) had five or more attorneys or agents.

    The report states that among survey respondents, "the mood for 2011 was cautiously optimistic" (the 2011 report noted that the mood in 2010 was "mixed"), with fewer respondents experiencing IP budget cuts and a greater percentage bringing in in-house support or outsourcing IP tasks.  Nevertheless, respondents did not expect to increase the number of patent families filed in 2012.  A majority of respondents cited passage of the Leahy-Smith America Invents Act, and the upcoming move to a first-to-file system, as the most important trend of 2012.  Other key trends for 2012 included cost containment (a repeat trend from last year's survey) and the maximization of IP revenue potential.

    Reflecting their cautious optimism, 18% of survey respondents said they filed more patent applications in 2011 than they expected (up from 9% in 2010) and 15% said they filed fewer patent applications (down from 19% in 2010) — 67% of respondents said they filed as many patent applications in 2011 as they expected (down from 72% in 2010).  The 2012 results were a significant improvement over those from inovia's first survey (released in 2010), where 41% of respondents said they filed fewer applications than expected in 2009.

    The 2012 report indicates a growing need for international patent protection, as 42% of respondents filed more than half of their patent applications abroad.  Respondents, however, continue to be selective with their filings abroad, with 37% of respondents filing corresponding applications in only 1-3 foreign countries and another 42% filed internationally in only 4-8 countries.  With regard to the countries in which respondents regularly filed, 21% added new countries to their list (up from 17% in 2010), with 28% adding China and smaller percentages adding India, Brazil, Russia, Taiwan, Chile, Korea, and South Africa (the latter four being new to the "newly added" list).  Only 17% of respondents dropped countries from their lists (down from 25% in 2010), with China and Europe each being dropped by 24% of respondents who pared down their lists, and a small percentage of respondents dropping Canada, Australia, India, and Italy from their lists.  Respondents who dropped China cited enforcement concerns as the primary reason, and those who dropped Europe cited the high cost of filing there.

    Interest in a unified European patent system rose again, with 93% of respondents in favor of the concept (as opposed to 88% in 2010).  In addition, the report notes that a large majority of respondents (99%) continue to rely on the PCT for foreign filing.  Of these respondents, 72% selected the EPO as an International Searching Authority (down from 89% in 2010), 42% selected the Korean IP Office (KIPO) (down from 43% in 2010), and 12% selected the Japan Patent Office (JPO) (down from 17% in 2010).

    With regard to IP budgets, fewer respondents reported budget cuts in the 2012 survey.  Only 20% of respondents said their IP budgets had been reduced in 2011, as opposed to 38% and 60% of respondents who noted that their budgets were cut in 2010 and 2009, respectively.  Respondents who experienced budget cuts, saw cuts that were less severe than in the past, with 15% losing more than 30% of their budget in 2011 as compared with the 18% who lost more than 30% of their IP budget in 2010.

    The report concludes by predicting that "[t]he cautious optimism identified in last year’s survey seems likely to continue in 2012."

  • By Donald Zuhn

    Federal Circuit SealLast month, the Federal Circuit affirmed a decision by the District Court for the District of New Jersey dismissing Plaintiff-Appellant Dr. George Pieczenik's complaint for failing to state a claim on which relief could be granted, as well as dismissing his charge of copyright infringement and denying his request for compulsory mediation and motion for recusal.

    Dr. Pieczenik is the inventor and owner of U.S. Patent No. 5,866,363, which is entitled "Method and means for sorting and identifying biological information, and which is directed to, inter alia, populations of oligonucleotides encoding peptide sequences of about 4 to about 12 L-amino acid residues, populations of peptides of about 4 to about 12 amino acid residues, and methods of producing a population of epitopic peptide sequences.  Dr. Pieczenik initiated the suit that led to the appeal by filing four separate complaints against 88 defendants, asserting infringement of the '363 patent as well as violation by some of the defendants of the Racketeer Influenced and Corrupt Organizations (RICO) statute.  The District Court dismissed the complaints sua sponte for failure to meet the minimum pleading requirements under the Federal Rules of Civil Procedure, and provided Dr. Pieczenik with an opportunity to correct the defects in a single consolidated amended complaint.  Following Dr. Pieczenik's filing of the consolidated amended complaint, all 88 defendants moved to dismiss the second complaint for failure to meet the requirements of Rule 12(b)(6) of the Federal Rules of Civil Procedure.  The District Court granted the motion, and Dr. Pieczenik appealed.

    The Federal Circuit begins by noting that while pro se litigants are generally held to a lesser standard than lawyers with regard to whether a complaint should be dismissed for failure to state a claim, a complaint must still contain sufficient factual matter, accepted as true, to state a claim to relief that is plausible on its face (citing Hughes v. Rowe, 449 U.S. 5 (1980), and Ashcroft v. Iqbal, 556 U.S. 662 (2009)).  With respect to Dr. Pieczenik's infringement claim, which the District Court dismissed, the Federal Circuit explained that:

    The complaint states that the '363 patent is infringed by defendant Invitrogen's sale of "vectors for the display of combinatorial libraries" and "DynaBeads for Phage Display and BioPanning," id. at 40; and by the purchase of combinatorial libraries produced by New England Biolabs by forty-one named defendants, namely: Abbott Laboratories, Abbott Laboratories, Inc., Amgen Inc., Amgen USA, Inc., AstraZeneca LP, AstraZeneca Pharmaceuticals LP, Baxter Diagnostics, Inc. (now Baxter Healthcare Corp.), Bayer Cropscience Inc., Biogen Idec Inc., Biogen Idec U.S. Corp., Boehringer Ingelheim Vetmedica, Inc., Boehringer Ingelheim Roxane, Inc., Bracco Diagnostics, Inc., Canon, U.S.A., Centocor Ortho Biotech Products, L.P., Centocor Ortho Biotech Services, LLC, Centocor Ortho Biotech, Inc., Daiichi Sankyo, Inc., E.I. du Pont de Nemours & Co., Dyax Corp., GE Healthcare Biosciences Bioprocess Corp., GE Healthcare Bio-Sciences Corp., GE Healthcare Inc., GE Healthcare Strategic Sourcing Corp., GlaxoSmithKline LLC, Howard Hughes Medical Institute, IDEXX Reference Laboratories, Inc., Invitrogen Corp., Millennium Pharmaceuticals, Inc., Monsanto Ag Products LLC, Monsanto Co., Novartis Corp., Novartis Pharmaceutical Corp., Novartis Vaccines and Diagnostics, Inc., OSI Pharmaceuticals, Inc., Shionogi Pharma Sales, Inc., Shionogi Pharma, Inc., Shionogi USA Holdings, Inc., Shionogi USA, Inc., Syngenta Crop Protection, Inc., and Syngenta Seeds, Inc.

    On appeal, Dr. Pieczenik argued that the District Court erred in dismissing his counts of patent infringement, suggesting that "[t]he fact that amino acid sequence SER-VAL-SER-VAL-GLY-MET-LYS-PRO-SER-PRO-ARG-PRO was isolated and made by several defendants [and that this] came out of the combinatorial library claimed in Plaintiff-Appellant's '363 patent" was sufficient "evidence of infringement."  However, the Federal Circuit noted that Dr. Pieczenik did "not discuss the criteria of patent infringement or identify which of the named defendants isolated or made the asserted sequence."  (Dr. Pieczenik also failed to specify which of the 92 claims of the '363 patent the defendants had infringed, arguing that each defendant infringed "one or more claims of the '363 patent.")  The Court therefore concluded that:

    No error has been shown in the district court's rulings as to the inadequacy of the complaint's recitation of the basis for the charges that any or all of the forty-one listed defendants infringed the '3[6]3 patent by purchasing libraries from NEB; that Invitrogen infringed the '3[6]3 patent through its sale of vectors for the display of combinatorial libraries and DynaBeads; or that any other defendant infringed the '3[6]3 patent by making, using, or selling any other product or process covered by the patent's claims.

    While not directly related to the patent infringement claims, Dr. Pieczenik's arguments that the District Court erred by denying his motion for recusal and determining that he failed to state the premises of a claim for copyright infringement are somewhat interesting.  With respect to the motion for recusal, the Federal Circuit explained that:

    Dr. Pieczenik recited seven grounds for recusal: (1) the possibility that Judge Pisano holds shares in any of the defendant public companies; (2) Judge Pisano's alleged favoritism toward opposing counsel; (3) Judge Pisano's denial of requested discovery; (4) Judge Pisano's failure to hold a Markman hearing; (5) Judge Pisano's "hidden agenda" as evidenced by consolidation of the four original actions into a single action; (6) Judge Pisano's failure to remove Milbank Tweed Hadley McCloy LLP as pro hac vice counsel in this matter; and (7) Judge Pisano's prejudices against pro se litigants, against Jewish litigants, against "scientists acting as lawyers," against inventors who litigate their patents, and against science generally.

    In affirming the District Court's denial of the recusal motion, the Federal Circuit concluded, however, that "Dr. Pieczenik has not shown any basis for questioning Judge Pisano’s impartiality . . . or that Judge Pisano is or may be personally biased or prejudiced against Dr. Pieczenik."

    In his motion in limine on the copyright claim, Dr. Pieczenik argued that the defendants violated his copyright by quoting, in their brief, statements made by him during a lecture to a biochemistry class at Rutgers University, relating to the ease and benefits of pro se litigation in federal court.  The Federal Circuit determined that to the extent that Dr. Pieczenik held a copyright to the lecture material, "this was a fair use of the quotation."

    The Federal Circuit concluded by affirming the District Court's refusal to grant Dr. Pieczenik 's request for compulsory mediation, finding that the District Court did not abuse its discretion in declining to compel mediation.

    Pieczenik v. Bayer Corp. (Fed. Cir. 2012)
    Nonprecedential disposition
    Panel: Circuit Judges Newman, Mayer, and Plager
    Opinion by Circuit Judge Newman

  • By Donald Zuhn

    WIPOEarlier this year, the World Intellectual Property Organization (WIPO) announced that International patent filings under the Patent Cooperation Treaty (PCT) were back on the rise following the 2007-09 recession (see "PCT and EP Filings on the Rise Again").  In particular, WIPO noted that filings had risen 4.8% from 2009 to 2010.  Last month, WIPO announced that filings would be up again in 2011, and that the number of international patent filings would set a new record.  According to the WIPO announcement, an estimated 181,900 PCT applications were filed last year.  Over the past five years, PCT filings look like this:

    Table                                 * estimate

    The United States is expected to hold onto the top ranking with 48,596 2011 filings, a 8% increase from the 45,008 applications that were filed in 2010.  China again saw the strongest growth in PCT filings, with applications up 33.4% to 16,406 in 2011.  Japan, Germany, and South Korea again rounded out the remainder of the top five with filings numbering 38,888 (up 21%); 18,568 (up 5.7%); and 10,447 (up 8.0%), respectively.

    When sorted by technical field, the top five fields for PCT filings in 2011 were:

    (1) Electrical machinery, apparatus, energy: 11,296 applications
    (2) Digital communication – 11,574
    (3) Medical technology: 10,753
    (4) Computer technology: 10,455
    (5) Pharmaceuticals: 7, 683

    The fields of biotechnology and organic fine chemistry each had more than 5,000 filings, with 5,232 and 5,283, respectively.  While the number of biotech filings rose slightly in 2011 from the 5,219 applications that were filed in 2010, the number of filings for organic fine chemistry was down in 2011 from the 5,511 applications filed in that field in 2010.  Organic fine chemistry was one of only four of the PCT's 35 technical fields that saw filings go down in 2011 (at least as far as WIPO's 2011 estimates are concerned).

    According to WIPO's figures, the top ten corporate PCT filers in 2011 were:

    (1) ZTE Corp. (China) – 2,826 applications
    (2) Panasonic Corp. (Japan) – 2,463
    (3) Huawei Technologies Co., Ltd. (China): 1,831
    (4) Sharp Kabushiki Kaisha (Japan): 1,755
    (5) Robert Bosch GmbH (Germany): 1,518
    (6) Qualcomm Inc. (U.S.): 1,494
    (7) Toyota Jidosha Kabushiki Kaisha (Japan): 1,417
    (8) LG Electronics Inc. (South Korea): 1,336
    (9) Koninklijke Philips Electronics N.V. (Netherlands): 1,148
    (10) Telefonaktiebolaget LM Ericsson (Sweden): 1,116

    Biotech/pharma companies making WIPO's Top 100 filers list included:  Procter & Gamble Co. (#24, 488 applications), Sumitomo Chemical Co. Ltd. (#27, 446), E.I. DuPont de Nemours & Co. (#29, 424), Dow Global Technologies Inc. (#34, 399), Novartis AG (#71, 200), F. Hoffmann-La Roche AG (#75, 189), Merck Patent GmbH (#94, 171), Sanofi-Aventis Deutschland GmbH (#96, 170), and Bayer CropScience AG (#99, 166).

    The five university PCT filers in 2011 were:

    (1) University of California (U.S.): 277 applications
    (2) Massachusetts Institute of Technology (U.S.): 179
    (3) University of Texas System (U.S.): 127
    (4) Johns Hopkins University (U.S.): 111
    (5) Korea Advanced Institute of Science and Technology (South Korea): 103

    The top three university filers in 2011 were identical to last year's top three.