Little Gem Life Sciences LLC v. Orphan Medical, etc. ( 2008 )


Menu:
  •                      United States Court of Appeals
    FOR THE EIGHTH CIRCUIT
    ___________
    No. 07-3285
    ___________
    Little Gem Life Sciences LLC,          *
    individually and on behalf of a        *
    class of persons similarly situated,   *
    *
    Appellant,                  *
    *       Appeal from the United States
    v.                               *       District Court for the
    *       District of Minnesota.
    Orphan Medical, Inc.; John H. Bullion; *
    and Timothy G. McGrath,                *
    *
    Appellees.                  *
    ___________
    Submitted: May 15, 2008
    Filed: August 11, 2008
    ___________
    Before WOLLMAN, MURPHY, and SMITH, Circuit Judges.
    ___________
    SMITH, Circuit Judge.
    Little Gem Life Sciences, LLC ("Little Gem") filed this securities class action
    against Orphan Medical, Inc. ("Orphan") on behalf of all individuals who held Orphan
    stock at the time Orphan was acquired by Jazz Pharmaceuticals, Inc. ("Jazz"). Little
    Gem alleged that Orphan and two of its principal executive officers, John H. Bullion
    and Timothy G. McGrath, negligently failed to disclose material information to
    Orphan's stockholders before asking the stockholders to approve Orphan's merger
    with Jazz, in violation of §§ 14(a) and 20(a) of the Securities Exchange Act of 1934
    (the "Exchange Act"), 15 U.S.C. §§ 78n and 78t, and Securities and Exchange
    Commission (SEC) Rule 14a-9, 17 C.F.R. 240.14a-9. The district court1 granted the
    defendants' joint motion to dismiss, finding that Little Gem failed to meet the
    heightened pleading standards required by the Private Securities Litigation Reform
    Act (PSLRA), 15 U.S.C. § 78u-4(b)(1) and (2). Little Gem appeals, arguing that the
    district court erred (1) by failing to convert Orphan's motion to dismiss into a motion
    for summary judgment, and (2) in finding that Little Gem's claims failed as a matter
    of law. We affirm.
    I. Background2
    Orphan is a specialty pharmaceutical company whose focus is on sleep
    disorders, pain, and other central nervous system disorders. At the time of the events
    giving rise to this lawsuit, Orphan's lead product was Xyrem. Bullion was Orphan's
    CEO and served on its Board of Directors ("Board"). McGrath was Orphan's CFO,
    Principal Accounting Officer, and Vice-President. In June 2004, Orphan merged, with
    shareholder approval, with Jazz, and in this merger, Jazz purchased all of Orphan's
    common stock at a price of $10.75 per share.
    Little Gem, the lead plaintiff of this putative class action, was an Orphan
    shareholder at the time of the merger and at all other relevant times. Little Gem
    brought this suit in 2006, alleging violations of §§ 14(a) and 20(a) of the Exchange
    Act and SEC Rule 14a-9.
    1
    The Honorable Ann D. Montgomery, United States District Judge for the
    District of Minnesota.
    2
    Because this matter was decided on a motion to dismiss, the facts are presented
    in the light most favorable to the plaintiffs. Davenport v. Farmers Ins. Group, 
    378 F.3d 839
    , 841 (8th Cir. 2004).
    -2-
    Orphan faced financial difficulties in the years leading up to 2005 and sought
    a company to buy out its stock. Orphan had several bidders, but these companies
    passed on the opportunity to purchase Orphan due to the company's uncertain future
    profitability. Orphan relied heavily on Xyrem, and it was uncertain whether Xyrem
    could have a broader medical application. Before the merger with Jazz, Orphan was
    testing Xyrem's effectiveness in treating fibromyalgia and had initiated Phase I of its
    Food and Drug Administration (FDA) clinical trial in June 2004. Orphan announced
    in its March 16, 2005, Form 10-K that it expected the results of Phase II of the clinical
    trial in the second half of 2005. While Phase II was completed by April 2005, the
    results would not be available for several more months. If Xyrem successfully
    completed Phase II, it would have to proceed to, and pass, Phase III of testing before
    the FDA would approve its use in the treatment of fibromyalgia.
    On April 18, 2005, Orphan's Board unanimously approved a merger agreement.
    Under the agreement, Jazz would acquire most of Orphan's publicly-owned stock, and
    Orphan would become a Jazz subsidiary. Shortly after the merger agreement was
    signed, Bullion, an Orphan board member, informed shareholders in a conference call
    that the proxy statement would explain why the company should merge before the
    Xyrem results were complete.
    On May 20, 2005, Orphan filed a proxy statement with the SEC in which
    Orphan provided details for the proposed merger. The proxy statement justified the
    merger, in part, based upon an opinion prepared by Banc of America Securities LLC
    ("Banc of America"), the financial advisor to Orphan's Board. Banc of America
    opined that the proposed merger was financially fair to the holders of Orphan common
    stock.
    On June 20, 2005, shortly before the shareholder vote on the merger, Jazz raised
    $100 million. The record does not provide a clear purpose for raising these funds.
    Orphan's shareholders approved the merger on June 22, 2005. In July 2005, the results
    -3-
    of the Xyrem trial were released, indicating that Xyrem could move to the next phase
    of testing. Following the announcement of these positive results, Little Gem brought
    this action, claiming that the defendants negligently made false or misleading
    statements. Little Gem contends that Orphan should have informed its shareholders
    of Xyrem's positive completion of the Phase II clinical trial and its moving to Phase
    III FDA testing before the shareholders voted on the merger agreement.
    Orphan moved to dismiss this action, and in support of its motion, Orphan
    asserted factual allegations that went beyond the face of Little Gem's complaint. The
    district court expressly declined to consider these additional facts but did utilize
    certain documents outside the pleadings to "establish context regarding the Xyrem
    clinical trial." The district court granted Orphan's motion to dismiss, finding that
    Little Gem failed to meet the heightened pleading standards mandated by the PSLRA.
    Little Gem now appeals.
    II. Discussion
    A. Standard for Evaluating the Motion to Dismiss
    Little Gem argues that the district court erred in not converting the motion to
    dismiss into a motion for summary judgment because the district court considered
    matters outside the pleadings. The district court stated that it considered information
    in public records to put the Xyrem drug testing into context. Because this information
    served a permissible limited purpose, we conclude that the district court did not err by
    not converting Orphan's motion to dismiss into one for summary judgment.
    "If, on a motion under Rule 12(b)(6) . . . , matters outside the pleadings are
    presented to and not excluded by the court, the motion must be treated as one for
    summary judgment under Rule 56." Fed. R. Civ. P. 12(d). The court, however, "may
    consider some materials that are part of the public record or do not contradict the
    complaint, as well as materials that are necessarily embraced by the pleadings."
    -4-
    Porous Media Corp. v. Pall Corp., 
    186 F.3d 1077
    , 1079 (8th Cir. 1999) (internal
    citation and punctuation omitted).
    The SEC filings relied upon by the district court for dates and details are the
    type of public records contemplated by Porous Media. The parties' dispute, however,
    concerns the extent to which the district court used these filings in deciding the
    present case. A number of our sister circuits have limited the purposes for which
    information in the public record may be considered on a motion to dismiss. See e.g.
    Bryant v. Avado Brands, Inc., 
    187 F.3d 1271
    , 1276 (11th Cir. 1999); Lovelace v.
    Software Spectrum, Inc., 
    78 F.3d 1015
    , 1018 (5th Cir. 1996); Kramer v. Time Warner
    Inc., 
    937 F.2d 767
    , 773–74 (2d Cir. 1991). We need not identify these various limited
    purposes because it is not necessary for the resolution of the matter before us. The
    district court did consider matters outside the pleadings by reviewing Orphan's SEC
    filings to obtain background facts regarding the Phase II Xyrem drug trial. Notably,
    the facts considered did not contradict Little Gem's complaint and were not critical to
    the outcome of Orphan's motion. The district court's decision appropriately rested on
    consideration of the parties' pleadings. Accordingly, we hold that the district court
    properly denied Little Gem's request to convert the motion to dismiss into a motion
    for summary judgment.
    B. Merits of Orphan's Motion to Dismiss
    Little Gem also asserts that the district court erred in determining that it failed
    to meet the heightened pleading standards required by the PSLRA. We disagree and
    affirm.
    "We review de novo the district court's dismissal of [Little Gem's] complaint."
    In re NVE Corp. Sec. Litig., 
    527 F.3d 749
    , 751 (8th Cir. 2008). Pursuant to the
    PSLRA, to state a claim, a complaint must "1) specify each statement alleged to have
    been misleading, [and] the reason or reasons why the statement is misleading, and 2)
    state with particularity facts giving rise to a strong inference that the defendant acted
    -5-
    with the required state of mind." 
    Id.
     (citations and punctuation omitted). "When
    considering a motion to dismiss, we take the complaint's material allegations as true
    and liberally construe the complaint in the plaintiff's favor." Davenport, 
    378 F.3d at 842
     (citation and punctuation omitted).
    Little Gem first argues that the heightened pleadings standards of the PSLRA
    do not apply to negligent misrepresentation actions because negligence is not a state
    of mind. We find this argument unpersuasive and unsupported by precedent. See
    United States v. Robinson, 
    439 F.3d 777
    , 780 (8th Cir. 2006) (rejecting the appellant's
    argument due to an absence of case law support).
    Little Gem next argues that the district court erred because it considered the
    facts alleged in the complaint in isolation rather than taken as a whole. In assessing
    whether a party has met the heightened pleading standards, the district court must
    consider all of the facts taken as a whole. See Cornelia I. Crowell GST Trust v. Possis
    Med., Inc., 
    519 F.3d 778
    , 782 (8th Cir. 2008) (requiring the district court to examine
    the facts "collectively"). The record before us does not support an argument that the
    district court did not properly consider the evidence as a whole.
    Essentially, Little Gem's case alleges that several comments in Orphan's proxy
    statement were false or misleading because Orphan's officers could have had access
    to the Xyrem test results and negligently failed to gain access. Had Orphan's
    executives advised themselves and the company's shareholders of the trial's probable
    success, perhaps a better stock price could have been attained in the Jazz merger.
    "Negligence requires a duty, an obligation of conduct to another person." Paul v.
    Missouri Pac. R. Co., 
    963 F.2d 1058
    , 1061 (8th Cir. 1992). Whether the defendants
    had early access to the raw test data is a disputed fact matter. But the issue before us,
    however, is whether Orphan's officers had a legal duty to search out and disclose such
    information while it remained under professional analysis in accordance with FDA
    -6-
    drug trial regulations. We hold that they did not. In fact, the blinding3 of the Xyrem
    trial was critical to ensuring the validity of the test results. See 
    21 C.F.R. § 314.126
    (b)(5) (stating that among the characteristics of "[a]n adequate and well-
    controlled study" is that "[a]dequate measures are taken to minimize bias on the part
    of the subjects, observers, and analysts of the data. The protocol and report of the
    study should describe the procedures used to accomplish this, such as blinding").
    Because there was no duty for the officers to find out the results of the study early, we
    conclude that Orphan and its officers cannot be negligent in failing to do so.
    III. Conclusion
    Accordingly, we affirm the judgment of the district court.
    ______________________________
    3
    In a double-blinded study, "neither the clinical trial participant nor the
    administering doctor knows whether the actual drug or a placebo is being used."
    Joanna R. Cerino, The Statutory Limits of Compassion: Can Treatment INDS Provide
    Meaningful Access to Investigational Drugs for the Terminally Ill?, 27 Temp. J. Sci.
    Tech. & Envtl. L. 79, 89 (2008).
    -7-