State of Louisiana, by and through its Attorney General James Caldwell v. AstraZeneca AB, AstraZeneca LP, AstraZeneca Pharmaceuticals LP, and Aktiebolaget Hassle ( 2020 )


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  •                               STATE OF LOUISIANA
    COURT OF APPEAL
    FIRST CIRCUIT
    NUMBER 2019 CA 0986
    STATE OF LOUISIANA, BY AND THROUGH ITS
    ATTORNEY GENERAL JEFF LANDRY
    VERSUS
    ASTRAZENECA AB, ASTRAZENECA LP, ASTRAZENECA
    PHARMACEUTICALS LP, AND AKTIBOLAGET HASSLE
    Judgment Rendered:      FJUL 0 2 2020
    Appealed from the
    Nineteenth Judicial District Court
    In and for the Parish of East Baton Rouge
    State of Louisiana
    Suit Number C637960
    Honorable Timothy E. Kelly, Presiding
    Jeff Landry                                   Counsel for Plaintiff/Appellant
    Attorney General                              State of Louisiana, by and through
    Elizabeth B. Murrill
    its Attorney General Jeff Landry
    Nicholas J. Diez
    Baton Rouge, LA
    Jerald P. Block
    Thibodaux, LA
    Alejandro Perkins
    Baton Rouge, LA
    Robert L. Salim
    Barrett Beasley
    Natchitoches, LA
    John Alden Meade
    Adam G. Young
    New Orleans, LA
    Patrick C. Morrow
    James P. Ryan
    Opelousas, LA
    Bradley C. Myers                                   Counsel for Defendants/ Appellees
    Linda R. Rodrigue                                  AstraZeneca AB, AstraZeneca LP,
    Amanda M. Collura -Day                             AstraZeneca Pharmaceuticals LP, and
    Baton Rouge, LA                                    Aktibolaget Hassle
    Michael P. Kelly
    Daniel M. Silver
    Daniel J. Brown
    Wilmington, DE
    I
    BEFORE: WHIPPLE, C. J., GUIDRY, AND BURRIS, JJ.
    Judge William J. Burris, retired, serving pro tempore by special appointment of the Louisiana
    Supreme Court.
    2
    GUIDRY, J.
    Plaintiff, the State of Louisiana, by and through its Attorney General, Jeff
    Landry, appeals from a trial court judgment granting summary judgment in favor
    of defendants, AstraZeneca AB, AstraZeneca LP, AstraZeneca Pharmaceuticals
    LP, and Aktibolaget Hassle,' and dismissing the State' s claims against them with
    prejudice.
    For the reasons that follow, we reverse and remand.
    FACTS AND PROCEDURAL HISTORY
    Average Wholesale Price Litigation
    On November 3, 2010, the State, by and through its Attorney General, James
    Caldwell3,
    D. "    Buddy"                  filed suit against multiple pharmaceutical companies,
    including AstraZeneca LP and AstraZeneca Pharmaceuticals LP, alleging that
    these defendant pharmaceutical companies had engaged in false, misleading,
    wanton, unfair, and deceptive acts and practices in the pricing and marketing of
    their prescriptive drug products. State v. Abbott Laboratories Inc., Suit Number
    596164, 19th Judicial District Court (Average Wholesale Price " AWP" Litigation).
    The State further alleged that the defendants' fraudulent pricing and marketing of
    their prescription drugs impacted elderly, disabled, and poor Louisiana citizens
    covered by the State' s Medicaid program by causing the State' s Medicaid agency
    to pay grossly excessive prices for the defendants' prescription drugs.
    According to the State' s petition, reimbursement for pharmacy -dispensed
    prescription drugs under the Louisiana Medicaid program is based on information
    supplied by defendants to industry reporting services.             This information includes
    the following prices indices: ( 1)         wholesale acquisition cost ( WAC); ( 2)        average
    wholesale price ( AWP);         and ( 3)   direct price.   The State alleged that from 1991-
    2
    We note that the spelling of defendant, Aktibolaget Hassle, varies throughout the record.
    However, for consistency, we will spell the name of defendant in this opinion as it appears in the
    caption of this proceeding and in the judgment at issue.
    In January 2016, Jeff Landry succeeded Attorney General James D. " Buddy" Caldwell.
    9
    2010,
    each of the named defendants knowingly, wantonly, and/ or intentionally
    provided or caused to be provided false and inflated AWP, WAC, and/ or direct
    price information for their individual drugs to various nationally known drug
    industry reporting services. These reporting services in turn published the pricing
    information to various reimbursers, such as Louisiana Medicaid, who contracted to
    receive the information as a basis for providing reimbursement to pharmacy
    providers who dispense prescription drugs.          According to the State, it relied on
    these artificially inflated AWP, WAC, and/ or direct prices in determining the
    amount it must reimburse providers, causing the State to pay excessive amounts for
    the prescription drugs.
    Additionally, the State alleged that the defendants created a " spread"      for
    their drugs, which is the difference between the AWP and WAC and the actual
    price of the prescription drug, and marketed that spread to physicians and
    pharmacies so they would purchase defendants' prescription drugs.             The State
    alleged that the defendants'   actions caused the State to pay millions of dollars in
    excess Medicaid payments.
    Therefore,   the State claimed violations of the Louisiana Unfair Trade
    Practices Act ( LUTPA), La. R. S.       51: 1401,               the Medical Assistance
    et seq.;
    Programs Integrity Law, La. R.S. 46: 437. 1,     et seq.; and the Louisiana Antitrust
    Law, La. R.S.   51: 121 et seq. The State also asserted claims for fi-aud, negligent
    misrepresentation, and unjust enrichment.
    Thereafter, on June 27, 2012,      the State and the AstraZeneca defendants
    entered into a settlement agreement and         release,
    thereby resolving the AWP
    litigation.
    Instant Toprol-XL litigation
    On March 18, 2015, the State filed the instant suit against defendants,
    AstraZeneca     AB,    AstraZeneca   LP,    AstraZeneca     Pharmaceuticals   LP,   and
    0
    Aktibolaget Hassle.        The petition alleged violations of the Louisiana Antitrust Law
    and the LUTPA arising from the manufacture, marketing, and sale of Toprol- XL,
    an extended- release drug used for the treatment of angina, hypertension, and
    congestive heart failure. Specifically, the petition alleged that defendants prevented
    generic   versions     of    Toprol- XL     from               the
    entering          market      by improperly
    manipulating patent filings and filing baseless patent infringement lawsuits to
    frustrate or delay market availability of generic equivalents, thus unlawfully
    monopolizing and/ or attempting to monopolize the domestic market for Toprol- XL
    and its generic bioequivalents such as metoprolol succinate. The State alleged that
    this unlawful scheme and anticompetitive conduct unreasonably restrained and
    injured competition by protecting Toprol-XL from generic competition in the
    relevant market.
    The State further alleged that as a result of defendants' conduct, it paid for
    Toprol-XL at prices significantly higher than what it would have paid if multiple
    competing and/ or generic versions of Toprol-XL were on the market.                        Also, the
    State alleged that as a result of defendants' unlawful scheme and anticompetitive
    conduct, it had been deprived of the benefits of free and unrestricted competition
    by being denied the opportunity to choose between branded Toprol- XL and generic
    alternatives,
    which would have cost thirty to forty percent less than branded
    Toprol-XL.      Instead,    the   State   alleged   it   was   forced    to     continue    to   pay
    supracompetitive prices for Toprol- XL,
    thereby causing it to sustain injury.
    Accordingly, the State sought restitution and treble damages, seeking to recover
    the amounts paid by the State for illegally obtained funds due to defendants'
    monopolistic    actions (    violation    of La. R. S.   51: 121,                and   unfair    and
    et seq.)
    deceptive trade practices ( violation of La. R.S. 51: 1401, et seq.).              The State also
    alleged claims for unjust enrichment.
    5
    On November 4, 2015, defendants filed exceptions raising the objections of
    no cause of action, no right of action, prescription, peremption, lack of subject
    matter jurisdiction,      and    vagueness
    or   ambiguity.     Following a hearing on
    defendants'    exceptions,
    the trial court signed a judgment on March 18,       2016,
    sustaining the exceptions raising the objections of no cause of action and no right
    of   action.    The State appealed the trial court' s judgment, and in State v.
    AstraZeneca AB, 2016- 1073 ( La. App. 1st Cir. 4/ 11/ 18), 
    249 So. 3d 38
    , this court
    reversed the trial court' s judgment and overruled the exceptions. The Louisiana
    Supreme Court subsequently denied writs in State v. AstraZeneca AB, 2018- 
    00766 La. 9
    / 21/ 18), 
    252 So. 3d 899
     and 2018- 0758 ( La. 9/ 21/ 18), 
    252 So. 3d 904
    .
    Thereafter, on November 8, 2018,
    the defendants filed an Answer and
    Affirmative Defenses, wherein they asserted, among other defenses, that the State
    had already been made whole with respect to the alleged damages due to the
    settlement between the AstraZeneca defendants              and   the   State   in the AWP
    litigation.
    On November 21,         2018,
    the defendants filed a motion for summary
    judgment, asserting several bases for summary judgment, including that the State' s
    claims    against them,
    which defendants characterized as claims that defendants
    unlawfully overcharged the State for pharmaceutical drugs, were compromised
    pursuant to the settlement agreement in the AWP litigation, and that the State' s
    claims are barred by res judicata. Pursuant to an agreement between the parties,
    the only issues for consideration at the hearing on defendants' motion for summary
    judgment were whether the AWP litigation and/ or res judicata barred the State' s
    claims in the instant case.
    Following a hearing on April 15, 2019, the trial court signed a judgment,
    finding that there was no genuine issue of material fact as to whether res judicata
    applies or whether the settlement agreement in the AWP litigation compromised
    A
    the claims made in the instant matter. The judgment therefore granted defendants'
    motion for summary judgment and dismissed all of the State' s claims against the
    defendants with prejudice. The State now appeals from the trial court' s judgment.
    DISCUSSION
    The general rule of res judicata in Louisiana is set forth in La. R. S. 13: 4231,
    which provides:
    Except as otherwise provided by law, a valid and final judgment is
    conclusive between the same parties, except on appeal or other direct
    review, to the following extent:
    1)   If the judgment is in favor of the plaintiff, all causes of action
    existing at the time of final judgment arising out of the transaction or
    occurrence that is the subject matter of the litigation are extinguished
    and merged in the judgment.
    2)   If the judgment is in favor of the defendant, all causes of action
    existing at the time of final judgment arising out of the transaction or
    occurrence that is the subject matter of the litigation are extinguished
    and the judgment bars a subsequent action on those causes of action.
    3)   A judgment in favor of either the plaintiff or the defendant is
    conclusive,      in any subsequent action between them, with respect to
    any issue actually litigated and determined if its determination was
    essential to that judgment.
    Under La. R. S.        13: 4231,   a second action is precluded when all of the
    following are satisfied: ( 1) the judgment is valid and final; ( 2) the parties are the
    same; (   3)   the cause or causes of action asserted in the second suit existed at the
    time of final judgment in the first litigation; and ( 4) the cause or causes of action
    asserted in the second suit arose out of the transaction or occurrence that was the
    subject matter of the first litigation.     Pierrotti v. Johnson, 11- 1317, p. 8 ( La. App.
    1st Cir. 3/ 19/ 12), 
    91 So. 3d 1056
    , 1063.
    While the doctrine of res judicata is ordinarily premised on a final judgment
    on the merits, it also applies where there is a transaction or settlement of a disputed
    or compromised matter that has been entered into by the parties.          Ortego v. State,
    Department of Transportation and Development, 96- 1322, p. 6 ( La. 2/ 25/ 97), 
    689 So. 2d 1358
    ,       1363.    Thus,
    compromises have the legal efficacy of the thing
    adjudged.
    Ortego, 96- 1322 at p. 6, 689 So. 2d at 1363; see also La. C. C. art. 3080.
    Louisiana Civil Code article 3071 defines a compromise as "               a    contract
    whereby the parties, through concessions made by one or more of there, settle a
    dispute or an uncertainty concerning an obligation or other legal relationship."            A
    party claiming res judicata based on a compromise must have been a party to the
    compromise, and the authority of the thing adjudged extends only to the matters
    the parties intended to settle.     Ortego, 96- 1322 at pp. 6- 7, 689 So. 2d at 1363.
    As a written contract, a compromise instrument is the law between the
    parties and must be interpreted according to the parties' intent. Ortego, 96- 1322 at
    p. 7, 689 So. 2d at 1363.     Interpretation of a compromise agreement is governed by
    the same general rules of construction applicable to contracts. Brown V. Drillers,
    Inc., 
    630 So. 2d 741
    , 748 ( La. 1994).
    When the words of a contract are clear and
    explicit and lead to no absurd consequences, no further interpretation may be made
    in search of the parties' intent. La. C. C. art. 2046.       Each provision in a contract
    must be interpreted in light of other provisions so that each is given the meaning
    suggested by the contract as a whole. La. C. C. art. 2050.
    A motion for summary judgment can be granted based on a finding of res
    judicata when there is no genuine issue as to any material fact. Brown, 630 So. 2d
    at 747, n.7.
    In determining whether summary judgment is appropriate, appellate
    courts review the evidence de novo under the same criteria that govern the trial
    court' s determination of whether summary judgment is appropriate.                   Lieux v.
    Mitchell,   06- 0382, p. 9 ( La. App. 1st Cir. 12/ 28/ 06), 
    951 So. 2d 307
    , 314, writ
    denied, 07- 0905 ( La. 6/ 15/ 07), 
    958 So. 2d 1199
    .     A motion for summary judgment
    is properly granted if, after an opportunity for adequate discovery, the motion,
    memorandum, and supporting documents show that there is no genuine issue as to
    material fact and that the mover is entitled to judgment as a matter of law.              La.
    C. C. P. art. 966( A)( 3).          When the issue before the court on the motion for
    summary judgment is one on which the party bringing the motion will bear the
    burden of proof at trial, the burden of showing there is no genuine issue as to
    material fact remains with the party bringing the motion.                      See La. C. C. P.   art.
    966( D)( 1);       Sova v. Cove Homeowner' s Association Inc., 11- 2220, p. 3 ( La. App.
    1st Cir. 9/ 7/ 12), 
    102 So. 3d 863
    , 866.
    In the instant suit, the defendants assert that the State' s claims are barred by
    res judicata due to the settlement agreement entered into between the State and
    defendants in the AWP litigation. The AWP settlement provides, in relevant part:
    2.   This agreement is intended to cover all pharmaceutical products
    manufactured,             distributed,      marketed,   co -marketed,    co -promoted
    and/ or sold by the Released Parties as defined herein, whether or not
    the drug was specifically named or referred to in the Litigation. These
    pharmaceutical products are referred to hereinafter as the " Covered
    Drugs."
    3. All: (
    a) conduct alleged in the Litigation, including that Defendant
    allegedly        engaged      in   false,    misleading,   willful,   wanton,    unfair,
    deceptive and unconscionable acts and practices in the pricing and
    marketing of prescription drug products; ( b) that Defendant allegedly
    engaged in a conspiracy in an effort to increase its market share; and
    c) potential claims of State concerning any conduct relating to any of
    the Released Parties ( as defined below) reporting, setting, publishing,
    or failure to object to the publication of another of [AWP, WA
    and/or Direct Price (" DP"),
    or any marketing activity relating to any
    such prices, constitutes the " Covered Conduct"
    that is addressed by
    this Agreement.            The Covered Conduct is expressly limited to: ( a)
    conduct which has occurred prior to the Effective Date of this
    Agreement; ( b)
    conduct as expressly alleged by the State in this
    Litigation and the potential claims referenced in the preceding
    sentence,        as though such conduct and potential claims had been
    alleged with respect to all of the Covered Drugs;                     and ( c)   claims
    concerning the State of Louisiana and its Medicaid Program.
    6. ... [     T] he State, on behalf of itself, and its officers,          employees,
    attorneys, agents, agencies, departments ...               political subdivisions and
    boards and commissions with any authority to initiate or maintain any
    claims         released    herein,    does     hereby fully    and    finally    release
    Defendant, and each of its past and present parents, and its associated
    companies, which means any corporation, partnership, limited liability
    company or other entity or combination thereof that directly or
    indirectly owns or controls Defendant, is owned or controlled by
    Defendant or is under common ownership or control with Defendant
    as well as any subsidiaries, divisions, partners, current and former
    9
    directors,   mangers,    officers,    employees, ...    agents,   shareholders,
    predecessors, divisions, executors, assigns, or legal representatives of
    each of the foregoing ( collectively, " Released Parties") from any
    known or unknown civil, regulatory,
    administrative or monetary
    claim,    action,
    suit or proceeding the State or any of its political
    subdivisions with any authority to initiate or maintain any claims
    released herein has or may have or could have asserted in the future
    under any source of law arising from or relating to the Covered
    Conduct.... This Release is expressly limited to the Covered Conduct
    and shall only release the Released Parties with respect to the
    Covered Conduct...
    The State shall not initiate or prosecute any civil
    or administrative actions,      qui tam lawsuits, whistleblower lawsuits,
    claims,   investigations,
    or any other type of proceeding against the
    Released Parties arising from or relating to the Covered Conduct.
    Emphasis added.]
    According to the        clear   and   unambiguous      language of the     settlement
    agreement read as a whole, the parties to the agreement intended only to settle and
    release     claims,    known or unknown, for " covered           conduct."     The agreement
    specifically and narrowly defines covered conduct to include: conduct alleged in
    the AWP litigation,
    including unlawful acts and practices in the pricing and
    marketing of prescription drug products and engaging in a conspiracy to increase
    its market share,
    and potential claims concerning any conduct relating to the
    reporting, setting, publishing, or failure to object to the publication of another of
    AWP,
    WAC, and/or Direct Price, or any marketing activity relating to any such
    prices.
    The agreement further limits the covered conduct to conduct occurring
    before the effective date of the agreement, to potential claims referenced in the
    preceding sentence, and to claims concerning the State and its Medicaid Program.
    Accordingly, the conduct at issue in the AWP settlement, as specifically
    described therein, was conduct relating to the unlawful price setting, and marketing
    of those prices, of defendants'           prescription drug products.       This interpretation
    conforms with not only the plain language of the settlement agreement but also
    with the claims asserted in the AWP litigation. The current claims of the State,
    however, do not arise from this conduct.               There is no complaint in the instant
    petition regarding the defendants' pricing of Toprol-XL, or specifically the AWP,
    10
    WAC, or direct price thereof, nor does the State complain about the marketing of
    those prices.
    Rather, the State' s claims, as detailed in its petition for damages,
    arise from defendants' unlawful manipulation of patent applications and patent
    litigation to delay and/ or prevent generic versions of Toprol- XL from entering the
    market.
    The State asserts that the actions of the defendants deprived the State of
    free and unrestrained competition by denying the State the opportunity to choose
    between branded Toprol-XL and lower-priced generic alternatives, which would
    have cost thirty to forty percent less than the branded Toprol- XL.                    The State
    alleges that had generic competitors been able to enter the market and compete
    with defendants, the State would have paid for lower-priced generics in place of
    the higher -priced brand name drug. Accordingly, the State asserts that the actions
    of the defendants caused the State to pay more for metoprolol succinate products
    than it otherwise would have paid had generic drugs been permitted to enter the
    market.
    Therefore, we find, based on the language of the settlement agreement, that
    the State' s current claims in the Toprol- XL litigation were not intended to be
    settled in the AWP settlement agreement, and that the conduct at issue in the
    instant litigation does not arise out of the covered conduct at issue in that
    agreement.          See Chauvin v. Exxon Mobil Corporation, 14- 0808, pp. 13- 14 ( La.
    12/ 9/ 14),   
    158 So. 3d 761
    , 770 ( finding that the transaction or occurrence            for res
    judicata purposes was defendant' s conduct and actions).               As such, the trial court
    erred in finding that res judicata
    applies4
    and in granting summary judgment in
    4
    We also note that another requirement of res judicata is that the actions involve the same
    parties.
    Furthermore, with regard to compromise agreements, the party claiming res judicata
    based on a compromise must have been a party to the compromise. In the instant case, while two
    of the defendants in the current suit were also parties to the AWP settlement agreement, two of
    the defendants were not.     Defendants assert that these two additional defendants are successors
    or assigns of the defendants who were parties to the AWP settlement, and therefore, they are the
    same parties for purposes of res judicata. However, there is no evidence or allegations
    supporting this assertion in the record.
    11
    favor of defendants, dismissing the State' s claims against them with prejudice.
    CONCLUSION
    For the foregoing reasons, we reverse the judgment of the trial court and
    remand this matter to the trial court for further proceedings.     All costs of this
    appeal are assessed to defendants, AstraZeneca AB, AstraZeneca LP, AstraZeneca
    Pharmaceuticals LP, and Aktibolaget Hassle.
    REVERSED AND REMANDED.
    12
    

Document Info

Docket Number: 2019CA0986

Filed Date: 7/2/2020

Precedential Status: Precedential

Modified Date: 10/22/2024