Mary Jasin v. Vivus, Inc. ( 2018 )


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  •                            NOT FOR PUBLICATION                           FILED
    UNITED STATES COURT OF APPEALS                        JAN 16 2018
    MOLLY C. DWYER, CLERK
    U.S. COURT OF APPEALS
    FOR THE NINTH CIRCUIT
    MARY JANE JASIN; THOMAS JASIN,                  No.    16-15893
    Plaintiffs-Appellants,          D.C. No. 5:14-cv-03263-BLF
    v.
    MEMORANDUM*
    VIVUS, INC.; LELAND F. WILSON;
    TIMOTHY MORRIS; PETER Y. TAM,
    Defendants-Appellees.
    Appeal from the United States District Court
    for the Northern District of California
    Beth Labson Freeman, District Judge, Presiding
    Argued and Submitted November 13, 2017
    San Francisco, California
    Before: GOULD and MURGUIA, Circuit Judges, and GRITZNER,** District
    Judge.
    Mary Jane and Thomas Jasin appeal the district court’s dismissal of their
    state and federal claims. We affirm.
    From 2012 to 2013, the Jasins invested heavily in shares of Vivus, Inc., a
    *
    This disposition is not appropriate for publication and is not precedent
    except as provided by Ninth Circuit Rule 36-3.
    **
    The Honorable James E. Gritzner, United States District Judge for the
    Southern District of Iowa, sitting by designation.
    drug developer. After the European Medical Agency’s Committee for Medicinal
    Products for Human Use (“CHMP”) denied an application to market Vivus’s new
    weight-loss drug, Vivus’s stock price dropped and the Jasins allegedly took a $2.8
    million loss. The Jasins filed a securities fraud suit in state court, but thereafter
    agreed to dismiss the case with prejudice on the Jasins’ motion in favor of a federal
    action. The Jasins later amended their federal court complaint to add state-law
    claims that had not been included in the prior dismissed state-court action. The
    district court dismissed the Jasins’ state-law claims as barred by res judicata and
    dismissed their federal securities fraud claims for failure to state a claim. We agree
    with the district court on both counts.
    The Jasins’ state-law claims that were newly asserted in this federal case are
    barred by res judicata. The Jasins do not dispute that under California law, all
    three elements of res judicata are satisfied here. See Fed. Home Loan Bank v.
    Countrywide Fin. Corp., 
    154 Cal. Rptr. 3d 873
    , 878 (Cal. Ct. App. 2013). Instead,
    the Jasins contend that the district court misapplied California law in construing
    their dismissal agreement, which they now argue implicitly waived res judicata.
    The parties’ agreement in the circumstances here was not controlling on the
    preclusive effects of the state court’s dismissal with prejudice. The record does not
    suggest that the parties “needed court approval of the settlement,” Villacres v.
    ABM Indus. Inc., 
    117 Cal. Rptr. 3d 398
    , 428 (Cal. Ct. App. 2010), that the
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    dismissal involved a “stipulated judgment,” Ellena v. State, 
    69 Cal. App. 3d 245
    ,
    250 (Cal. Ct. App. 1977), or otherwise that “the stipulation [was] a part of the
    decision” such that “it is impossible to construe the effect of the decision without
    considering the effect of the stipulation,” Miller & Lux v. James, 
    179 P. 174
    , 178
    (Cal. 1919). In any event, the Jasins represented explicitly to the district court that
    a dismissal agreement’s waiver of res judicata must be “express,” but they now
    argue on appeal that the court should not have applied that standard. The Jasins
    may not complain on appeal of purported errors below for which they are
    responsible. See Deland v. Old Republic Life Ins. Co., 
    758 F.2d 1331
    , 1336 (9th
    Cir. 1985).
    The Jasins’ federal securities fraud claims were also properly dismissed.
    The Jasins primarily take issue with four instances of allegedly fraudulent
    statements on appeal.1 None of these statements amounted to a material
    misrepresentation or omission. “[S]ection 10(b) and Rule 10b-5 prohibit only
    misleading and untrue statements, not statements that are incomplete.” In re Rigel
    Pharm., Inc. Sec. Litig., 
    697 F.3d 869
    , 880 n.8 (9th Cir. 2012). Vivus “was not
    obligated to disclose each and every step it took when interacting with regulators.”
    In re Atossa Genetics Inc. Sec. Litig., 
    868 F.3d 784
    , 800 (9th Cir. 2017). And
    1
    We decline to assess the adequacy of statements included in the background
    section of the Jasins’ briefs but not referred to in their arguments. See Fed. R.
    App. P. 28(a)(8)(A).
    3
    these statements fall far short of the heightened pleading requirements for scienter.
    See Zucco Partners, LLC v. Digimarc Corp., 
    552 F.3d 981
    , 990–91 (9th Cir.
    2009).
    First, the Jasins complain that Vivus stated that “[t]he 120-day questions are
    consistent with the issues previously raised in the FDA review process.” That
    statement was accurate. The issues raised by the FDA and CHMP were similar,
    though the FDA was ultimately satisfied with Vivus’s plan to conduct a post-
    approval study while the CHMP was not.
    Second, the statement that Vivus “never talked about a preapproval
    cardiovascular safety study” with the FDA was not improper. The Jasins argue
    that this statement was not inherently dishonest but “became misleading” when
    paired with the statement above, which Vivus issued months earlier. We disagree.
    As Vivus repeatedly warned, there was no guarantee that the CHMP would handle
    its cardiovascular concerns in the same way that the FDA had handled them.
    Third, Vivus’s disclosure made on three occasions that the CHMP “may”
    require a pre-approval cardiovascular study was not misleading or false. It was
    possible, but not guaranteed, that such a study would be needed until the CHMP
    issued its decision requiring the study in October 2012. The 80-day report showed
    that the Rapporteur and Co-Rapporteur disagreed about whether a cardiovascular
    study would be needed. Their joint 120-day report said the issue precluded
    4
    approval “at the present time” and “need[ed] to be further discussed,” but their
    next report said merely that the lack of a study “should be further justified.” In any
    event, the Rapporteur and Co-Rapporteur spoke for only two of the CHMP’s 29
    voting members, and the CHMP required a pre-approval study by a divided vote of
    19 to 10.
    Fourth, the statements that there was “nothing new to report” and that the
    drug “was looking real good for approval” are also unobjectionable. The Jasins do
    not argue that there might have been something “new to report” at that time. And
    the generic statement that the chances of approval were “looking good” falls in the
    category of “mildly optimistic, subjective assessment[s]” that are insufficient for a
    securities fraud claim. In re Cutera Sec. Litig., 
    610 F.3d 1103
    , 1111 (9th Cir.
    2010).
    AFFIRMED.
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