•     By Kevin E. Noonan

    There is something about biotechnology that brings out the Cassandras (which is being kind; "Chicken Little" is a more accurate characterization) in people who oppose it.  Whether motivated by a renewed "vitalism" (see "Science Fiction in The New York Times") or some kind of green (or Green) impulse, the temperature of the debate always seems overheated.

    Thomas_jim
    Jim Thomas (at right), general manager of the Erosion, Technology and Concentration (ETC) Group, a Canadian environmental group, has in the past raised the alarm against Dr. J. Craig Venter, one of the most audacious (and successful) of the 20th century breed of biotechnology scientist/entrepreneurs (see "Patenting Life (Really)").  The issue (or threat, depending on your prejudices):  Dr. Venter’s attempts to produce (and patent) a synthetic microorganism.  The work is based on Mycoplasma genitalium, a bacterium whose genome encodes a mere 482 genes.  The idea is to identify a core set of essential genes by systematically subtracting genes from the organism to see which ones are required for viability.  Earlier this year, Dr. Venter’s group reported that it had Etc_group
    been able to delete 101 of those genes.  Once the set of minimal genes has been identified, they can be introduced into a bacterial "shell," and this would result for the first time in a synthetic organism that does not exist in nature.

    Venter_craig
    Of course, Dr. Venter (at right) and his group has applied for patents on this organism; examples of such patent applications are published International Application Publication No. WO 2007/047148 (published April 26, 2007), and U.S. Patent Application Publication No. 2007/0122826 (published May 31, 2007).  Representative claims include:

    1.  A set of protein-coding genes that provides the information required for growth and replication of a free-living organism under axenic conditions in a rich bacterial culture medium, wherein the set lacks at least 40 of the 101 protein-coding genes listed in Table 2, or functional equivalents thereof, wherein at least one of the genes in Table 4 is among the lacking genes; wherein the set comprises between 350 and 381 of the 381 protein-coding genes listed in Table 3, or functional equivalents thereof, including at least one of the genes in Table 5; and wherein the set comprises no more than 450 protein-coding genes.

    20.  A free-living organism that can grow and replicate under axenic conditions in a rich bacterial culture medium, whose set of genes consists of the set of any of claims 1-15.

    The claims thus encompass the specific minimal gene set itself (that defines the genetic content of the bacteria) as well as the bacteria itself.  On their face they would appear to satisfy the criteria of usefulness, novelty, and non-obviousness, and since they are directed to bacteria, they should not implicate the usual concerns voiced by those in opposition to human gene patenting.  Although a much greater technical tour de force, these claims hearken back to the distinctions drawn by the U.S. Supreme Court in deciding in Diamond v. Chakrabarty that a recombinant Pseudomonas aeruginosa bacteria was patentable.

    Knight_tom_2
    Mr. Thomas thinks otherwise.  In a press release (which was also cited on the WIRED Science blog), he opines that "overly-broad" patent claims could "stunt" synthetic biological research.  (Interestingly WIRED characterizes ETC as a "biotech watchdog" rather than as an environmental group.)  Mr. Thomas characterizes the Venter claims as a "legal rats’ nest," including claims to "basic research" such as "adding synthetic DNA to a living organism."  These sentiments are echoed by Dr. Tom Knight (at left), a computational biologist from the Massachusetts Institute of Technology, who calls the claims "absurdly, ridiculously broad" — the piece is silent on Dr. Knight’s credentials for making this assessment.  ETC’s propaganda is seasoned with catchy sound bites, such as analogizing Dr. Venter’s efforts with Bill Gates’ allegedly predatory activities in the computer sphere, and warning that Dr. Venter is trying to create a "Microbesoft" monopoly.

    Church_george_2
    Harvard geneticist (and "godfather" of the synthetic biology field) Dr. George Church (at right) once more brings some perspective and sagacity to the discussion.  He rightly notes that the claims would need to be narrowed significantly before they could be granted.  He sets forth a list of "unlikely" events that would need to occur for the horrors ETC envisions to occur:

    1. Patent offices worldwide decide that the claims are useful and non-obvious without restrictions,
    2. These claims are upheld in court challenges,
    3. The market favors the patent holders and no work-arounds are found,
    4. The resulting monopoly discourages innovation,
    5. The government doesn’t interfere with such a monopoly.

    Dr. Church also reminds us that "even Microsoft couldn’t stop Google, Firefox, Java, Linux, etc."

    Something Dr. Church did not mention, and which deserves mentioning, is that it is extremely difficult to obtain the kind of broad patent claims that ETC and its sympathizers fear.  An important reason comes from the inherent complexity of biological systems and the relatively little we know about how these systems work.  "Work arounds" can be difficult in the mechanical and electrical arts, because the underlying technology can be predictable and there can in fact be one good solution to a problem that is the most efficient, economical, reliable, and compatible with existing systems.  Biology, in contrast, seems to operate on the principle that "when life closes a door, it opens a window"; in a word, living systems adapt.  Because of that, the instances of broad patent claims to fundamental biological methods, reagents, compounds, or processes are rare (and Patent Docs would appreciate our readers pointing out any such claims).  So the practical chances of Dr. Venter "stifling the field of synthetic biology" are unrealistic.  Particularly because, even if all of Dr. Church’s unlikelihoods were to occur, the patent term would expire in less than twenty years, and by that time the field would have moved on using design-arounds motivated by Dr. Venter’s own patent claims.

    Endy_drew_3
    The WIRED article also quotes MIT biological engineer Dr. Drew Endy (another synthetic biology godfather; at left) as referencing one of his own papers, published in 2005 in the journal Molecular Systems Biology, "which describes the design, construction, and testing of engineered genomes . . . [e]verything described in this paper is in the public domain."  The article concludes that since the paper is in the public domain, the techniques for producing synthetic organisms cannot be hampered by anything Dr. Venter is trying to do.  This part of the article is evidence of the vast disconnect between the understanding of scientists, even eminent scientists, and patent law.  While Dr. Endy’s work in his paper is important and perhaps groundbreaking, it is directed to a bacterial virus (the T7 bacteriophage), not a bacteria, and thus its relevance to the patentability of Dr. Venter’s claims is tenuous at best.  It is not worth mentioning (since it seems to occur so often) that there is not a word in the WIRED article from a patent attorney on the subject.  Regardless of such an attorney’s opinion on the underlying patentability of Dr. Venter’s work (and patent attorneys are not monolithic on the subject; after all, Dan Ravicher of the Public Patent Foundation (PUBPAT) opposes patenting some forms of biotechnology invention), at least the article would have been more informed about the legal issues and probabilities regarding the patentability of Dr. Venter’s work.  One can only speculate that what these groups want is not light but heat, in view of the vehemence of their opposition, which is as good an explanation as any for the tone and tenor of their comments.

  •     By Sherri Oslick

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


    Monsanto Company et al. v. Gastel

    3:07-cv-05119; filed December 12, 2007 in the Western District of Missoui

    Infringement of U.S. Patent Nos. 5,352,605 ("Chimeric Genes for Transforming Plant Cells Using Viral Promoters," issued October 4, 1994) and RE39,247 ("Glyphosate-tolerant 5-enolpyruvylshikimate-3-phosphate Synthases," issued August 22, 2006) based on defendant’s use of soybean seed produced from earlier planted Roundup Ready® soybean seed.  View the complaint here.


    AstraZeneca Pharmaceuticals LP et al. v. Mylan Pharmaceuticals Inc.

    1:07-cv-00805; filed December 11, 2007 in the District Court of Delaware

    AstraZeneca Pharmaceuticals LP et al. v. Sun Pharmaceutical Industries Ltd. et al.
    1:07-cv-00806; filed December 11, 2007 in the District Court of Delaware

    AstraZeneca Pharmaceuticals LP et al. v. Sandoz Inc.
    1:07-cv-00807; filed December 11, 2007 in the District Court of Delaware

    AstraZeneca Pharmaceuticals LP et al. v. Par Pharmaceutical Inc.
    1:07-cv-00808; filed December 11, 2007 in the District Court of Delaware

    AstraZeneca Pharmaceuticals LP et al. v. Apotex Inc. et al.
    1:07-cv-00809; filed December 11, 2007 in the District Court of Delaware

    AstraZeneca Pharmaceuticals LP et al. v. Aurobindo Pharma Ltd. et al.
    1:07-cv-00810; filed December 11, 2007 in the District Court of Delaware

    AstraZeneca Pharmaceuticals LP et al. v. Cobalt Pharmaceuticals Inc. et al.
    1:07-cv-00811; filed December 11, 2007 in the District Court of Delaware

    Astrazeneca Pharmaceuticals LP et al. v. Cobalt Pharmaceuticals Inc. et al.
    2:07-cv-00815; filed December 13, 2007 in the Middle District of Florida

    The complaints in these cases are substantially identical.  Infringement of U.S. Patent No. RE37,314 ("Pyrimidine Derivatives," issued August 7, 2001) following a paragraph IV certification as part of defendants’ filing of an ANDA to manufacture a generic version of AstraZeneca’s Crestor® (rosuvastatin calcium, used to treat high cholesterol).  View the Mylan Pharmaceuticals Inc. complaint here.


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

    0:07-cv-61800; filed December 10, 2006 in the Southern District of Florida

    Sanofi-Aventis et al. v. Apotex Inc. et al.
    1:07-cv-00792; filed December 6, 2007 in the District Court of Delaware

    The complaints in these cases are substantially identical.  Infringement of U.S. Patent No. 4,661,491 ("Alfuzosine Compositions and Use," issued April 28, 1987) following a paragraph IV certification as part of Apotex’s filing of an ANDA to manufacture a generic version of plaintiffs’ Uroxatral® (alfuzosin hydrochloride, used to treat benign prostatic hyperplasia).  View the Delaware complaint here.


    Sanofi-Aventis Deutschland GmbH et al. v. Glenmark Pharmaceuticals Inc., USA et al.

    2:07-cv-05855; filed December 7, 2007 in the District Court of New Jersey

    Infringement of U.S. Patent No. 5,721,244 ("Combination of Angiotensin-Converting Enzyme Inhibitors with Calcium Antagonists As Well As Their Use in Drugs," issued February 24, 1998) following a paragraph IV certification as part of Glenmark’s filing of an ANDA to manufacture a generic version of plaintiffs’ Tarka® (trandolapril and verapamil hydrochloride, used to treat hypertension).  View the complaint here.


    Pamlab, L.L.C. v. Cura Pharmaceutical Company, Inc. et al.

    1:07-cv-02546; filed December 7, 2007 in the District Court of Colorado

    Infringement of U.S. Patent No. 6,528,496 ("Compositions Treating, Preventing, or Reducing Elevated Metabolic Levels," issued March 4, 2003) based on Cura’s manufacture and sale of its Folnate and Folnate Plus, allegedy generic versions of Pamlab’s Foltx® (vitamin B12, vitamin B6, and folic acid, used to treat hyperhomo-cysteinemia).  View the complaint here.


    Pfizer, Inc. et al v. Cobalt Pharmaceuticals, Inc.

    1:07-cv-12257; filed December 7, 2007 in the District Court of Massachusetts

    Pfizer Inc. et al. v. Cobalt Pharmaceuticals, Inc.
    1:07-cv-00790; filed December 6, 2007 in the District Court of Delaware

    The complaints in these cases are substantially identical.  Infringement of U.S. Patent No. 5,273,995 ("[R-(R*R*)]-2-(4-fluorophenyl)-beta, delta-dihydroxy-5-(1-methylethyl-3-phenyl-4-[(phenylamino) carbonyl]- 1H-pyrrole-1-heptanoic acid, its lactone form and salts thereof," issued December 28, 1993) based on Cobalt’s filing of an NDA (under § 505(b)(2) of the Food, Drug and Cosmetic Act) to manufacture a generic version of Pfizer’s Lipitor® (atorvastatin calcium, used to treat high cholesterol and heart disease).  View the Delaware complaint here.


    Abbott Laboratories v. Sandoz, Inc.

    3:07-cv-05820; filed December 6, 2007 in the District Court of New Jersey

    Infringement of U.S. Patent Nos. 6,511,678 ("Controlled Release Formulation of Divalproex Sodium," issued January 28, 2003), 6,528,090 (same title, issued March 4, 2003), 6,713,086 (same title, issued March 30, 2004), and 6,720,004 (same title, issued April 13, 2004) following a paragraph IV certification as part of Sandoz’s filing of an ANDA to manufacture a generic version of Abbott’s Depakote® ER (divalproex sodium, used to treat manic episodes associated with bipolar disorder, epilepsy, and migraine headaches).  View the complaint here.

  • Calendar
    January 4-8, 2008 – 25th Annual National CLE Conference (law Education Institute, Inc.) – Vail, CO

    January 9, 2008 – Patent Claim Construction (Law Seminars International) – San Francisco, CA

    January 14-15, 2008 – Patent Law Institute (Practising Law Institute) – New York, NY

    January 25-26, 2008 – Buying, Selling and Licensing Patents: New Case Law, Rules, Legislation and Markets (Law Seminars International) – San Francisco, CA

    January 28-29, 2008 – Patent Law Institute (Practising Law Institute) – San Francisco, CA

    January 30-February 1, 2008 – Pharma/Biotech IP Due Diligence (American Conference Institute) – New York, NY***

    February 15, 2008 – Patent Claim Construction (Law Seminars International) – Chicago, IL

    February 25-26, 2008 – Pharma/Biotech Patent Claim Drafting and Prosecution (American Conference Institute) – New York, NY***

    February 25-26, 2008 – Strategic Intellectual Property Planning (American Conference Institute) – Scottsdale, AZ

    March 30-April 1, 2008 – Advanced Courses (Patent Resources Group) – Bonita Springs, FL

    April 3-5, 2008 – Advanced Courses (Patent Resources Group) – Bonita Springs, FL

    June 17-20, 2008 – BIO International Convention (Biotechnology Industry Organization) – San Diego, CA

    ***Patent Docs is a media sponsor of this conference or CLE.

  •     By Robert Dailey

    Invitrogen_2
    Life sciences companies Invitrogen and Genetic Applications (GA) have settled the patent infringement suit that GA filed last year alleging infringement of U.S. Reissued Patent No. RE39,220.

    Genetic_applications
    The ‘220 patent is directed to methods of transplanting DNA into a eukaryotic genome to yield hematopoietic cell lines.  These cell lines are generally useful for simulating an in vivo micro-environment in vitro.  Thus, they are useful for drug discovery and toxicology screening.

    Invitrogen had been using the patented technology since the late 1990s.  GA knew of the infringement, and had even sued Invitrogen in 1999 for infringement of the predecessor patent to the reissue, but because of a defect in the complaint, the suit was dismissed.

    Seal
    Later in 1999, GA filed for a reissue of the patent on which it had sued Invitrogen.  The reissue patent was not issued until 2006.  At that point, GA again filed suit against Invitrogen – this time in the Eastern District of Texas’ "Rocket Docket."

    In a summary judgment motion
    filed in October, Invitrogen argued that the reissue patent is unenforceable due to laches.  GA knew of Invitrogen’s infringement in 1999 and waited seven years to sue.  Of course, GA might argue that the laches clock should be tolled during the 7-year-long reissue proceedings at the PTO.

    This brings up an interesting wrinkle related to reissue proceedings from 35 U.S.C. § 252 (emphasis added):

    The surrender of the original patent shall take effect upon the issue of the reissued patent, and every reissued patent shall have the same effect and operation in law, on the trial of actions for causes thereafter arising, as if the same had been originally granted in such amended form, but in so far as the claims of the original and reissued patents are substantially identical, such surrender shall not affect any action then pending nor abate any cause of action then existing….

    Hence, as far as the law is concerned, GA continued to have standing to maintain its infringement suit from 1999, even though it had requested a reissue.  By waiting on the sidelines for seven years, GA became a victim of the laches clock.  It may have been better to maintain the suit and ask the Court to stay proceedings pending the results of the reissue proceedings.

    Details of the settlement have not become public.  Nevertheless, GA settled the case without ever filing a brief answering Invitrogen’s motion for summary judgment on the laches issue.  This likely bodes well for Invitrogen.

  • Biotechnology Industry Organization (BIO) The Biotechnology Industry Organization (BIO) will be holding its annual BIO International Convention on June 17-20, 2008 in San Diego, CA.  Founded in 1993, BIO is a nonprofit association seeking supportive biotechnology policies on behalf of more than 1,100 biotechnology companies, state and international affiliates, and related organizations, as well as providing business development services for many emerging biotech companies.  According to BIO, the BIO International Convention serves to educate the public and policymakers about biotechnology, while fostering partnering meetings and other business development activities to keep the biotech industry growing.  A preliminary schedule of events Bio_international_convention
    for the Convention can be obtained here.  As part of the Convention, more than 1,700 biotech companies, organizations, and institutions will participate in the BIO Exhibition.  A list of exhibitors can be found here.  Information regarding registration pricing can be obtained here.

  • New York #2 Practising Law Institute (PLI) will be holding its 2nd Annual Patent Law Institute on January 14-15, 2008 in New York, NY and on January 28-29, 2008 in San Francisco, CA.  A live webcast of the San Francisco session will also be available.  The two-day conference consists of six one-hour plenary sessions of broad interest to patent lawyers and a separate breakout track consisting of six one-hour sessions focusing on one of three patent practice sub-groups: patent prosecution; patent litigation; and patent transactions.  The plenary sessions will cover:

    • Recent Supreme Court and Federal Circuit decisions and subsequent District Court applications of those decisions.
    • U.S. Patent and Trademark Office rule changes.
    • Strategic business use of patent portfolios in view of KSR and USPTO rule changes and other recent events.
    • An international update on PCT trends and practices.
    • A judges panel discussion of recent appellate decisions and the impact on pending litigation; resolution of discovery disputes and other motion practice issues; and the use of ADR.
    • A corporate counsel panel discussion on patent business and legal concerns.

    San Francisco #5 Breakout tracks will cover:

    • Prosecution:
      • The impact of new USPTO rules initiatives;
      • USPTO biotech/pharma trends; and
      • A discussion of EFS-Web and USPTO Web forms.
    • Litigation:
      • The impact of recent appellate decisions;
      • Litigation in the Eastern District of Texas;
      • Practical guidelines for e-discovery management; and
      • Industry spotlights on pharma/biotech, electronics/semiconductor, and software patent litigation.
    • Transactions:
      • Drafting opinions of counsel in the wake of KSR and In re Seagate;
      • Critical business considerations of a license agreement;
      • The impact of MedImmune on licensing;
      • Eighteen hidden dangers in your patent license agreement; and
      • Patent valuation for litigation and licensing and patent auctions.

    A program schedule and list of speakers for the New York Patent Law Institute can be found here, and a program schedule and list of speakers for the San Franscisco Patent Law Institute can be found here.

    Practising Law Institute (PLI) #1 The registration fee for the conference is $1,495 (group discounts are available for groups of 4-14 members of the same organization).  Those interested in registering for the conference can do so at the PLI website.

  •     By Robert Dailey

    Just two years ago, the world of patent law (and maybe even Michael Crichton) waited for the Supreme Court to reconsider the standard for patentable subject matter – at least with respect to process claims.

    Supreme_court_building_2
    The Supremes had granted cert. on the following question:  "Whether a patent instructing a party to ‘correlate test results’ can validly claim a monopoly over a basic scientific relationship used in medical treatment such that a doctor infringes the patent by looking at a test result and thinking about that relationship?"  In other words, could Metabolite Laboratories, Inc. claim a valid patent monopoly over its discovery that high levels of homocysteine in the blood correlate with deficiencies of folic acid and vitamin B12 in humans?

    Lab_corp_logo
    In the end, the Supreme Court punted, and we never got an answer.  After all, cert. had been granted on an issue that the defendant, LabCorp, had never properly raised in the District Court litigation.

    Last week, though, the District Court confirmed that the injunction that issued after the trial is no longer in force because the patent-in-suit, U.S. Patent No. 4,940,658, has expired.  Meanwhile, the litigation continues as the two parties continue to litigate the issue of damages.

  •     By Suresh Pillai —

    Morphotek
    Last month, Morphotek, Inc., a subsidiary of Eisai Co., Ltd. based in Exton, Pennsylvania, announced that it had been granted U.S. Patent No. 7,235,643 ("Antibodies and methods for generating genetically altered antibodies with high affinity," issued June 26, 2007).  This is the eleventh U.S. Patent awarded to Morphotek, Inc.

    Eisai
    Prior to cell division, gene duplication is accomplished by the parent cell’s replication of the cell’s genetic material.  Errors in replication can lead to mutations among the duplicated genes; however, DNA repair mechanisms, such as mismatch repair (MMR), normally repair such mutations prior to cell division.  MMR is a proofreading mechanism by which the cell checks the genetic coding between the two copies of the genetic material to ensure that the genes are, in fact, copies of one another.  Normally, cell division occurs only upon completion of MMR.  In cells where MMR is dysfunctional, mutations accumulate through the genome to the point where sibling cells have traits different from the parents.  Morphogenics is a technology whereby the MMR process is selectively regulated within a living host.  Through the regulation of morphogenics and targeted mutation, scientists can accelerate cellular evolution, thereby creating unique organisms ideal for the study of disease pathogenesis or other commercial applications.

    The ‘643 patent covers both Morphotek’s proprietary human MORPHODOMA® technology, which combines an ex vivo immunization with morphogenics.  The resultant antibodies naturally target specific disease-associated antigens.

    The ‘643 patent issued from U.S. Application No. 10/243,130 which was filed on September 13, 2002 and which was a continuation-in-part of U.S. Application No. 09/707,468, filed November 7, 2000, which is now U.S. Patent No. 6,808,894.  Independent claim 1 recites:

    1.  A method for producing a monoclonal antibody having an increased affinity for the antigen to which it binds relative to a monoclonal antibody comprising a heavy chain variable region comprising SEQ ID NO: 18, the method comprising substituting Alanine at the sixth position of SEQ ID NO:18 with Proline, whereby the affinity of the produced monoclonal antibody for said antigen is increased.

    Suresh Pillai, Ph.D., is a molecular biologist and a third-year law
    student at DePaul University College of Law.  Dr. Pillai
    was a member of MBHB’s 2007 class of summer associates, and is currently working as a law clerk at MBHB.

  •     By Donald Zuhn

    Leahy_patrick_2
    The Intellectual Property Owners Association (IPO) announced today that IPO President Marc Adler has written a letter to Senator Patrick Leahy (at right), urging the Chairman of the Committee on the Judiciary to delete a provision from the Senate Patent Reform Act (S.1145) that would require applicants to submit "a search report and other information and analysis relevant to patentability."  The IPO President informed Chairman Leahy that IPO members have found this provision to be "particularly problematic."  While conceding that the Applicant
    Quality Submissions required under the bill’s provision are supported by the Bush Administration, Mr. Adler noted that such submissions "have attracted little or no support from IPO members and have raised significant opposition."

    Ipo_2_2
    According to Mr. Adler, the quality submissions provision, if passed into law, would lead to an increase in the number of inequitable conduct charges, which in turn would result in an increase in litigation costs, thereby "deterring innovators from using the patent system to protect new technology."  Mr. Adler added that the Senate bill’s provision codifying the "important to a reasonable patent examiner" standard for materiality in inequitable conduct cases would not resolve the problems raised by the quality submissions provision.

    Adler_marc_2
    In his letter, Mr. Adler (at right) outlined the IPO’s position that the quality submissions provision would "require applicants to search the prior art in every case before filing their applications."  Mr. Adler explained that while many IPO members perform routine pre-filing searches, such searches "should not be required by law."  In addition, because of the "highly subjective" nature of searches, the manner in which applicants conducted their searches would raise inequitable conduct charges in "nearly every case" if the quality submissions provision were passed.  The IPO President concluded his letter by arguing that the provision’s requirement to characterize prior art identified in mandated pre-filing searches would "force the applicant to act as a patent examiner for his own invention" and "create an even more fertile ground for inequitable conduct charges."

    For additional information on this topic, please see:

  •     By Jason Derry —

    Eisai
    Eisai Co., Ltd. and MGI PHARMA, Inc. have announced that Eisai will acquire MGI PHARMA for approximately $3.9 billion.  Eisai is a research-based company focusing on discovery, development, and marketing of therapeutic products in the fields of neuroscience, gastrointestinal disorders, and oncology.  MGI PHARMA is a biopharmaceutical company that focuses on oncology.  MGI PHARMA currently has a number of products on the market in the U.S., including Aloxi® (palonosetron hydrochloride) for injection, Mgi_pharma_2
    Dacogen® (decitabine) for injection, and Gliadel® Wafer (polifeprosan 20 with carmustine implant), and also has a large pipeline of therapeutic agents in various clinical trials.  Eisai’s acquisition of MGI PHARMA is in line with its strategic plan of strengthening its worldwide position in the field of oncology.

    Jason Derry, Ph.D., who graduated with honors from DePaul University
    College of Law, is a molecular biologist and founding author of Patent Docs.