•     By Jason Derry —

    Roche
    Roche Holding AG has
    announced an agreement with Synosis Therapeutics in which
    Synosis will have rights to five drug candidates that Roche is no longer
    developing.  Four of the drugs are in
    Phase I clinical trials.  According to
    the Press Release, the drugs relate to schizophrenia, cognitive disorders,
    Parkinson's Disease, drug dependency, and pain.

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

  •      By Jason Derry —

    Elusys
    Elusys Therapeutics, Inc. has
    announced an exclusive license with Pfizer Inc. to collaborate in the development of new therapeutics for infectious
    diseases.  The agreement relates to the
    use of Elusys' HP Antibody® technology.

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

  •     By Jason Derry —

    Ecopia
    Ecopia BioSciences Inc. and
    Caprion Pharmaceuticals Inc. have
    announced the intent to merge and form a new company that will focus on oncology and infectious
    disease.

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

  •     By Jason Derry —

    Wyeth
    Pharmacopeia and Wyeth have announced that the two
    companies have agreed to an exclusive license relating to the
    development and commercialization of therapeutics from Pharmacopeia's JAK3
    inhibitor technology.  Under the
    agreement, Pharmacopeia has the right to therapeutics relating to
    dermatological and ocular diseases by topical administration, while Wyeth has
    rights to develop products related to all other indications and forms of
    administration.

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

  •     By Mark Chael

    In an
    opinion by Circuit Judges Prost and Dyk handed down on December 29, 2006, the
    U.S. Court of Appeals for the Federal Circuit held that the U.S.
    District Court for the District of Arizona had incorrectly construed the claim term "dispensing" in U.S. Patent No. 6,352,861 (the '861 patent) as requiring "direct dispensing."  The CAFC, therefore, vacated the lower
    court's judgment of non-infringement and remanded the case.  In dissent was Circuit Judge Lourie, who
    agreed with the lower court's claim construction.

    63528613The '861 patent at issue in
    this case claims
    methods and related devices for performing various biological assays on
    laboratory slides, including immunostaining, using bar code readers to identify
    reagents and slides, as well as computers to coordinate the procedures.  On February 11, 2003, Ventana brought suit
    against BioGenex alleging infringement of claims 1-3, 5, 6, and 8 of the '861 patent.  Following a Markman hearing
    (Ventana Med. Sys., Inc. v. BioGenex Labs., Inc., No. 03-CV-92 (D. Ariz. 2005)), in which the District Court construed the claim term "dispensing"
    to mean "direct dispensing," Ventana stipulated to non-infringement, reserving
    its right to appeal the District Court's claim construction.

    Ventana Medical Systems
    All of the
    asserted claims of the '861 patent contain the term "dispensing" and the sole issue on appeal was the District Court's construction of that term to require "direct dispensing."  As construed by the District Court, "direct dispensing" means that a reagent is dispensed directly from a reagent container onto a
    slide containing a specimen, without using an intermediate transport system to "sip" reagent from a reagent bottle and "spit" the reagent onto the slide.  According
    to the District Court, the context of the term in the claims led to the narrow
    interpretation, since the claims state that a reagent "in" a reagent container
    is dispensed "onto" a slide.  The District Court also determined that a narrower construction was warranted in view of the written description and figures of the '861 patent, which disclose
    embodiments in which reagents are dispensed from the bottom of reagent containers onto the
    slides.  BioGenex also alleged that the
    inventors had disclaimed indirect dispensing during the prosecution of related
    patent applications.

    Federal Circuit Seal
    The CAFC
    reviewed the claim construction issue de novo (see Cybor Corp. v FAS Techs.,
    Inc.
    , 138 F.3d 1448 (Fed. Cir. 1998) (en banc)) and determined that the ordinary
    and customary meaning (see Phillips v. AWH Corp., 415 F.3d
    1303 (Fed. Cir. 2005) (en banc)) of the claim term "dispensing" would not be limited to "direct
    dispensing" by a person of ordinary skill in the art.  The CAFC disagreed with the District Court's reliance on the words "in" and "onto" in support of the narrowing interpretation to require "direct dispensing," stating that there is
    nothing in the language of the claims to limit the term "dispensing."  The CAFC also did not agree with
    BioGenex that certain general statements distinguishing the invention from the
    prior art in the Background section of the '861 patent constituted a disavowal
    of claim coverage by the inventors (see e.g., Honeywell Int'l., Inc. v. ITT Indus.,
    Inc.
    , 452 F.3d 1312 (Fed. Cir. 2006) and SciMed Life Sys., Inc. v. Advanced
    Cardiovascular Sys., Inc.
    , 242 F.3d 1337 (Fed. Cir. 2001).  In addition, the CAFC dismissed BioGenex's
    allegation that since the disclosure only showed direct dispensing, the claims
    should be so limited.  The CAFC has "repeatedly warned against confining the claims to [the specific] embodiments
    [described in the specification]" (see Phillips, 415 F.3d at 1323).  Also, the CAFC noted that "each claim does not necessarily cover every
    feature disclosed in the specification" and "[w]hen the claim addresses only
    some of the features disclosed in the specification, it is improper to limit
    the claim to other, unclaimed features."  Ventana, slip op. at 11, citing
    Phillips
    at 1327; Golight, Inc. v. Wal-Mart Stores, Inc., 355 F.3d 1327, 1331
    (Fed. Cir. 2004); and E-Pass Techs., Inc. v. 3Com Corp., 343 F.3d 1364, 1370
    (Fed. Cir. 2003).  Finally, the CAFC
    dismissed BioGenex's allegations of prosecution history disclaimer because it was based on statements made in a
    related application, stating that the doctrine "generally does not apply when the
    claim term in the descendant patent uses different language."  Ventana, slip op. at 12, citing Invitrogen
    Corp. v. Clontech Labs., Inc.
    , 429 F.3d 1052, 1078 (Fed. Cir. 2005);
    ResQNet.com, Inc. v. Lansa, Inc., 346 F.3d 1374, 1383 (Fed. Cir. 2003); and
    Advanced Cardiovascular Sys., 265 F.3d at 1305-06.  Because the CAFC determined that the related applications upon which BioGenex relied in alleging prosecution history disclaimer used different claim language than the claims at issue, Ventana's statements during prosecution of its related application were not applicable
    to the present case.

    The case was remanded to the District Court for further proceedings in light of the CAFC's claim construction.

    Ventana Med. Sys., Inc. v. BioGenex Labs. (Fed. Cir. 2006)
    Panel: Circuit Judges Lourie, Dyk, and Prost
    Opinion by Circuit Judge Prost; dissenting opinion by Circuit Judge Lourie

    Additional Disclaimer:  MBHB was involved in the prosecution of the '861 patent.  To the extent that this case summary contains any opinions,
    the opinions would be of Dr. Chael and not Ventana Medical Systems, Inc. or MBHB.

  •     By Jason Derry —

    Amgen
    Amgen Inc. has announced that it will
    collaborate with Cytokinetics to generate
    small-molecule therapeutics for treating heart failure.  In particular, the agreement relates to
    discovery, development, and commercialization of compounds that activate
    cardiac myosin.  Cytokinetics has
    identified a particular cardiac myosin activator, CK-1827452, that is currently
    its lead drug candidate relating to cardiovascular disease.  As part of the agreement, Amgen has announced
    that it has acquired an option on CK-1827452, which has completed two Phase 1
    clinical trials.  According to the press
    release, Cytokinetics will receive an up-front licensing fee of $42
    million.  In addition, Amgen purchased
    about $33 million of Cytokinetics stock, giving Amgen about 7% of the company.

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

  •     By Jason Derry —

    Sigma-Aldrich
    Sigma-Aldrich has announced that it has agreed to give Pfizer a
    non-exclusive, worldwide license to use DNA-directed RNAi (ddRNAi) for research
    purposes.  Sigma-Aldrich has an exclusive
    license to the ddRNAi technology (excluding the right to develop ddRNAi for
    therapeutic use in humans) from Benitec Ltd. and Australia's CSIRO (Commonwealth Scientific and
    Industrial Research Organization).

    Benitec
    Benitec is an Australian biotechnology company that
    focuses on DNA-directed gene silencing. According to its website, Benitec has 10 issued patents relating to
    ddRNAi.  Benitec's first ddRNAi patent in
    the U.S. is 6,573,099.

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

  •   By Sherri Oslick

    Gavel
    We have reported here and here on Savient
    Pharmaceuticals, Inc. v. Sandoz, Inc. and Upsher-Smith Laboratories, Inc.
    ,
    2:06-cv-05782, filed December 4, 2006 in the District Court of New Jersey.  The district court judge had granted, then
    vacated, the temporary restraining order sought by Savient to prevent Sandoz
    from taking any actions to market, launch, sell or distribute generic
    Oxandrin® (oxandrolone).  Judge
    Sheridan denied Savient's request for a preliminary injunction, and the issue
    went up to the CAFC on appeal.  Savient
    filed its appeal on December 8th, and on December 12th the CAFC granted a TRO.  On December 28th, the CAFC denied the
    preliminary injunction, leaving Sandoz free to launch its generic product.

    The patents in suit are U.S. Patent Nos. 5,872,147;
    6,090,799; 6,670,351; 6,576,659; and 6,828,313; all directed to uses of
    oxandrolone.

  •     By Sherri Oslick

    Gavel
    About Court Report: Each week we will report briefly
    on recently filed biotech and pharma patent cases.  A few interesting cases will be selected for
    periodic monitoring, providing our readers with an opportunity to follow the
    progress of these cases.

    Celgene Corp. and Novartis Pharmaceutical Corp. et. al.
    v. Teva Pharmaceuticals USA Inc. et. al.

    3:06-cv-06154; filed December 21, 2006 in the District
    Court of New Jersey

    Infringement of reexamined U.S. Patent No. 6,355,656
    ("Phenidate Drug Formulations Having Diminished Abuse Potential,"
    issued March 12, 2002; assigned to Celgene and licensed exclusively to
    Novartis in certain fields of use) following a paragraph IV certification as
    part of Teva's filing of an ANDA to manufacture a generic version of Novartis'
    Focalin® (dexmethylphenidate hydrochloride, used to treat attention deficit
    hyperactivity disorder).  Teva's ANDA had
    been stayed based on Celgene/Novartis' filing of related case 3:04-cv-04030
    asserting infringement of a related patent; the stay is to expire on January 9,
    2007.  View the complaint here.


    LEK D.D. v. Bristol-Myers Squibb Co. and Watson
    Pharmaceuticals, Inc.

    2:06-cv-00547; filed December 29, 2006 in the Eastern
    District of Texas

    Infringement of U.S. Patent Nos. 6,740,775
    ("Crystalline Sodium Salt of Pravastatin," issued May 25, 2004) and
    7,078,558 ("Crystals of the Sodium Salt of Pravastatin," issued July
    18, 2006) based on BMS's manufacture and
    sale of its Pravachol® (pravastatin sodium, used to reduce cholesterol levels)
    and Watson's manufacture and sale of a generic counterpart.  View the complaint here.

  •      By Donald Zuhn

    USPTO Seal
    The USPTO announced that the Patent Office will be closed
    on Tuesday in view of President Bush's proclamation that there be a National
    Day of Mourning for President Gerald R. Ford on January 2, 2007.  Because the Patent Office will consider Tuesday to be a "Federal
    holiday" under 35 U.S.C. § 21 and 37 C.F.R. §§ 1.6, 1.7, 1.9, 2.2(d),
    2.195, and 2.196, any action or fee due on January 2, 2007 will be considered as being timely
    filed if the action is taken, or the fee is paid, on Wednesday, January 3, 2007.  Correspondence deposited as Express Mail or transmitted
    through the patent Electronic Filing System on January 2, 2007 will be considered as filed on
    the date of deposit or date indicated on the Acknowledgment Receipt.