• Calendar_20
    August 23-24, 2007 – Current Issues in Complex IP Licensing: Business and Legal Factors for Licensing Transactions (Law Seminars International) – Seattle, WA

    August 24, 2007 – Managing Patent Prosecution and Litigation: New Regulations, Rules and Challenges, along with Practical Tips for Success (law Seminars International) – San Francisco, CA

    September 18-19, 2007 – Pharma/Biotech Patent Boot Camp (American Conference Institute) – San Francisco, IL***

    September 24-25, 2007 – Biosimilars 2007 (Scherago International, Inc.) – George Washington University, Washington, D.C.

    September 26-27, 2007 – Advanced Forum on Biotech Patents (American Conference Institute) – Boston, MA***

    September 27-28, 2007 – Biotechnology: Business and Legal Developments (Law Seminars International) – Seattle, WA

    October 12, 2007 – Intellectual Property Law Summit 2007 (West LEGALWorks and Intellectual Property Law Association of Chicago) – Chicago, IL

    October 25-26, 2007 – Biotech and Pharma Public-Private Partnerships Forum (American Conference Institute) – Washington, D.C.***

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

  • Seattle #2 Law Seminars International (LSI) will be holding a conference entitled "Biotechnology: Business and Legal Developments" on September 27-28, 2007 in Seattle, WA.  The conference will address legal and business issues facing the biotech industry, including funding approaches, licensing and collaboration trends, merger and acquisition developments, and evolving intellectual property and regulatory issues.  In particular, the conference's speakers will offer presentations on the following topics:

    • Life science incubators and other funding strategies.
    • Merger and acquisition developments.
    • The relationship between government and industry.
    • Strategies for winning regulatory approval.
    • Recent patent litigation and reform proposals.
    • Private sector joint research agreements.
    • Product partnering and platform technology deals.
    • Partnering with universities.
    • Legal and regulatory risks in sales and marketing.
    • Disclosure requirements for public companies.

    LSI - Law Seminars International - blue The agenda for LSI's Biotechnology conference can be found here.  A complete brochure for this conference, including an agenda, list of speakers, and registration form can be downloaded here.

    The registration fee ranges from $497.50 (students and new employees) to $995 (regular tuition).  Discounts are available for government employees and groups of two or more registrants.  Those interested in registering for the conference can do so here.

  • San Francisco #5 Law Seminars International (LSI) will be holding a conference entitled "Managing Patent Prosecution and Litigation: New Regulations, Rules and Challenges, along with Practical Tips for Success" on August 24, 2007 in San Francisco, CA.  The conference will analyze the implications of on-going Patent Office and legislative changes and address strategic patent portfolio development and patent litigation management from an in-house perspective across major technology areas.  In particular, the conference's speakers will offer presentations on the following topics:

    • Recent patent reforms and pending proposals in Congress and the U.S. Patent and Trademark Office, and the implications of these reforms and proposals for prosecution and litigation.
    • Best practices in drafting claims and disclosures in light of recent patent law changes.
    • Portfolio development, with in-house counsel of software, network and security; biotechnology and pharmaceuticals; and semiconductors and hardware industries.
    • Major recent court cases: How they effect damages and the economics of licensing.

    LSI - Law Seminars International - blue The agenda for LSI's Managing Patent Prosecution and Litigation conference can be found here.  A complete brochure for this conference, including an agenda, list of speakers, and registration form can be downloaded here.

    The registration fee ranges from $347.50 (students and new employees) to $695 (regular tuition).  Discounts are available for government employees and groups of two or more registrants.  Those interested in registering for the conference can do so here.

  • Seattle #1 Law Seminars International (LSI) will be holding a conference entitled "Current Issues in Complex IP Licensing:  Business and Legal Factors for Licensing Transactions" on August 23-24, 2007 in Seattle, WA.  The conference will address business and legal factors that must be addressed to achieve a mutually beneficial licensing arrangement.  In particular, the conference's speakers will offer presentations on the following topics:

    • Current themes and recent cases in complex licensing.
    • Major recent patent cases and impact on licensing strategies.
    • The intersection of antitrust law and intellectual property protection.
    • Royalty terms.
    • Virtual property.
    • On-line licensing structures.
    • Payment systems.
    • Developments in new media advertising.
    • Cross-border transactions with China.
    • Legal ethics in a digital age.
    • The anatomy of a complex license.

    LSI - Law Seminars International - blue The agenda for LSI's Complex IP Licensing conference can be found here.  A complete brochure for this conference, including an agenda, list of speakers, and registration form can be downloaded here.

    The registration fee ranges from $497.50 (students and new employees) to $995 (regular tuition).  Discounts are available for government employees and groups of two or more registrants.  Those interested in registering for the conference can do so here.

  • Aventis Prevails over Impax in Riluzole Dispute

        By Robert Dailey —

    Sanofiaventis_large
    On remand from the Federal Circuit (see "Impax Labs., Inc. v. Aventis Pharm. Inc. (Fed. Cir. 2006)"), the District Court found that U.S. Pat. No. 5,527,814 is not anticipated by the prior art.  Particularly, the Court found that the anticipating reference cited by Impax does not enable one of skill in the art to use rizulole to treat amyotrophic lateral sclerosis (ALS).

    Riluzole
    The District Court had already reached this conclusion once, finding that the prior art failed to show that rizulole would be effective for treating ALS.  At the time of the Court’s initial decision, this finding was probably sufficient to demonstrate that the anticipating reference was not enabled.

    But between the date of the District Court’s initial opinion and the date of the appeal, the Federal Circuit articulated a more nuanced approach to determining whether anticipating prior art is enabled.  See Novo Nordisk Pharms. v. Bio-Tech. Gen. Corp., 424 F.3d 1347 (Fed. Cir. 2005); Rasmusson v. SmithKline Beecham, 413 F.3d 1318 (Fed. Cir. 2005).  Under the more nuanced approach, the District Court cannot find a lack of enablement simply based on the anticipating reference’s failure to show effectiveness.  According to the Federal Circuit, effectiveness is more relevant to questions of utility.  To determine lack of enablement, the fact-finder must look to whether the anticipating reference teaches one of ordinary skill in the art to practice the invention without undue experimentation, where undue experimentation is evaluated in light of the eight Wands factors.

    In most situations, this distinction probably makes little difference.  In fact, Judge Rader dissented in part from the Federal Circuit opinion because he believed that the District Court’s factual findings supported the validity of the Aventis patent under the old standard as well as the new standard.  But the majority preferred to remand the case to the District Court for re-evaluation in light of Rasmusson.

    Impax_laboratories
    In last week’s opinion, the District Court found that the anticipating prior art cited by Impax still lacked enablement.  While Rasmusson has changed the formal process for evaluating enablement, it probably will have little outcome-determinative effect in most cases.  Commentators have long recognized that utility and enablement are related.  Though the two doctrines rely on different legal tests, evidence that demonstrates lack of utility will often also demonstrate lack of enablement.  But in the context of anticipation, the federal courts have held that enablement, and not utility, is the relevant inquiry for determining whether an anticipating reference precludes patentability.

    We may ponder, though, whether this nuanced distinction carries much of a punch.  After all, enablement and utility are both malleable concepts.  The former is judged against an eight-factor balancing test, while the latter requires one to wade through the shifting sands of Brenner v. Manson, In re Brana, and In re Fisher.  Moreover, is there a doctrinally sound reason why we look to enablement but not to utility in evaluating the value of an anticipating reference?  In looking back at old CCPA cases, see, e.g., In re Hoeksema, 399 F.2d 269 (C.C.P.A. 1968), patent courts appear to have applied this "enabling disclosure" requirement in a flexible manner that dually encompassed considerations of both enablement and utility.  And especially when the claims-in-suit are method claims, wouldn’t we want to consider whether the anticipating reference failed to demonstrate the utility of the method?  After all, how can one of skill in the art make and use something that is not useful?

    Impax Labs., Inc. v. Aventis Pharm. Inc., No. 02-581-JJF (D. Del. 2007)
    Opinion by District Judge Farnan

    Robert Dailey, Ph.D., is a physical chemist and regular Patent Docs
    contributor.  Dr. Dailey, who recently completed his studies at the
    University of North Carolina School of Law and passed the patent
    registration exam, will be joining MBHB this fall.

    Additional Disclaimer:  MBHB represented Aventis in the above litigation.  To the extent that this case summary contains any opinions, the opinions would be of Dr. Dailey and not Aventis or MBHB.

  •     By Donald Zuhn

    Uspto_seal
    Further to our earlier report, the United States Patent and Trademark Office (USPTO) provided more details on Wednesday regarding the addition of the Japan Patent Office (JPO) to the Priority Document Exchange (PDX) program.  In particular, the USPTO announced that for U.S. applications filed on or after July 28, 2007, the USPTO will automatically attempt to electronically retrieve a copy of any JPO priority document claimed in the Oath, Declaration, or Application Data Sheet, to which priority is claimed in a U.S. application.  For U.S. applications filed before July 28, 2007, applicants must file a request (form PTO/SB/38) for the USPTO to retrieve a copy of the JPO priority document.  To transmit U.S. priority documents to the JPO, the U.S. priority document must (a) be published or patented or (b) have cleared national security review.  For the second category of U.S. priority documents, applicants must also submit written authorization to transmit the priority document (use of form PTO/SB/39 is recommended).

  •     By Christopher P. Singer

    Genentech
    Genentech
    announced in an August 2, 2007 press release that the Hart-Scott-Rodino waiting period that applied to its acquisition of Tanox, Inc. has expired, and that the acquisition is now completed.  The merger agreement, originally approved by Tanox shareholders on January 15, Tanox_logo
    2007, provides a cash payment of $20 per share of Tanox common stock held at closing (about $919 million total).  Tanox shares are no longer traded on the NASDAQ exchange.

    Xolair
    Since the mid-1990’s Genentech and Tanox have collaborated with each other and with Novartis on the development and marketing of Xolair® (Omalizumab).  Xolair is an anti-IgE monoclonal antibody approved for treatment of patients with moderate-to-severe allergic asthma.  Tanox had previously received royalty payments from Genentech and Novartis.  As a result of the merger, Genentech eliminates the cost of this royalty and acquires Novartis’ profit share and royalty payments which Novartis previously paid to Tanox.

  • Denial of PI for Interim Patent Term Extension Affirmed

        By Sherri Oslick

    Animated_logo
    In a nonprecedential opinion, the Federal Circuit affirmed the District Court of Delaware’s denial of Somerset’s request for preliminary injunction to compel the Director of the USPTO to grant an interim patent term extension.  Somerset is the owner of U.S. Patent No. RE34,579 ("Method of treating depression," issued April 5, 1994), which is set to expire on August 18, 2007.  Somerset sought an extension in term of the ‘579 patent after receiving FDA approval to market Emsam®, a transdermal patch containing selgline; the ‘579 patent covers methods of treating depression using Somerset’s patch.

    I2_t_2
    On April 27, 2006, pursuant to 35 U.S.C. § 156(d)(1), which authorizes an applicant to file for an extension of patent term based on regulatory delay, Somerset filed an application for term extension with the USPTO.  On February 21, 2007, Somerset filed a request for interim extension under § 156(e)(2), which authorizes the Director, where a patent is set to expire before a certificate of extension can be either granted or denied, to extend the term of a patent for up to one year until such a decision is made, provided that the patent is eligible for extension.

    Dudas_1000
    On May 22, 2007, with no decision from the USPTO in hand, Somerset filed suit in the District Court of Delaware to compel the Director to act on – and grant – its request for interim extension.  Somerset also moved for a preliminary injunction for the same relief.  The District Court denied the preliminary injunction on June 29, 2007.  Somerset appealed to the CAFC, moving for, and receiving, an expedited briefing schedule.  The motion for expedited briefing was granted on July 12, and on that same day the Director denied Somerset’s application for interim extension as well as its original application for term extension under § 156(d)(1).

    In view of the USPTO’s decision, Sommerset withdrew the portion of its appeal directed at compelling the Director to act on its request for interim extension, and as such, the CAFC dismissed that portion of the appeal as moot.  Sommerset nevertheless maintained the appeal insofar as it sought injunctive relief to compel the Director to grant the interim extension.

    The CAFC affirmed the lower court’s denial of preliminary injunction on the basis that Somerset could not show a reasonable likelihood of success.  The statute authorizing the Director to grant an interim extension, noted the CAFC, only did so in situations where a certificate of extension could not be granted or denied prior to expiration of the patent at issue.  Because the USPTO had already denied Somerset’s original application for extension, the Director had no authority to grant an interim extension, and Somerset therefore had no reasonable likelihood of success on the merits.  The CAFC did add in a footnote, however, that nothing in their opinion was intended to address the merits of the Director’s decision to deny a term extension.

    Somerset Pharmaceuticals, Inc. v. Dudas (Fed. Cir. 2007)
    Nonprecedential disposition
    Panel: Chief Judge Michel and Circuit Judges Prost and Moore
    Opinion by Circuit Judge Moore

    Additional information regarding this case can be found at Orange Book Blog .

  •     By Christopher P. Singer

    Alnylam
    In an August 1, 2007 press release, Alnylam Pharmaceuticals, Inc. announced that the European Patent Office has issued a Rule 51(4) notification for European Patent 1 407 044 ("Tuschl II") which relates to RNA interference (RNAi) technology.  In the same release, Alnylam also stated that the corresponding application in Australia has been granted (AU 2002235744).  Alnylam acquired it’s interest in this patent portfolio through a license agreement with the Max Planck Society, through the licensing agent of the society, Max Planck Innovation GmbH.

    Epoepc
    According to the press release, the European Patent is expected to issue within the next six months, and covers compositions, methods, and uses of small interfering RNAs (siRNAs).  More particularly, Alynlam’s website provide a PDF document of 25 claims here, which the press release indicates are the claims that have been granted.  Briefly, Alnylam states in the press release that the claims include:

    • siRNAs with a double stranded region formed from two RNA strands with a length of 19-23 nucleotides;
    • one or more 3′-overhangs at the ends of the double-stranded molecule;
    • compositions with chemical modifications on the 3′-end of the siRNA to protect against degradation and/or the use of one or more nucleotide modification, such as 2′-O-Me or 2′-F, without any limitation to the number of such modifications; and
    • the use and pharmaceutical compositions of such an siRNA molecule to modulate the function of mammalian or pathogen-derived genes both in vitro and in vivo.
  •     By Jason Derry —

    Mytogen
    Advanced Cell Technology, Inc. has announced that it will acquire Mytogen, Inc., which has completed a Phase I clinical trial relating to its Myoblast Program for treating heart failure.  The Myoblast Program is a stem cell therapy approach to treating a patient having heart failure, in which autologous myoblasts are obtained from the patient, expanded for two to three weeks, and transplanted back into the patient’s heart.  Mytogen has been given permission from the FDA to proceed to Phase II trials.  Advanced Cell Technology, which recently announced that it has successfully derived a human embryonic stem cell line without destroying an embryo, is focused on using stem cell technology in the field of regenerative medicine.

    Advanced_cell_technology_2

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