Gursheel Dhillon v. Endo Pharmaceuticals , 617 F. App'x 208 ( 2015 )


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  • ALD-200                                           NOT PRECEDENTIAL
    UNITED STATES COURT OF APPEALS
    FOR THE THIRD CIRCUIT
    ____________
    No. 14-3377
    ____________
    UNITED STATES OF AMERICA ex rel.
    GURSHEEL S. DHILLON,
    Appellant
    v.
    ENDO PHARMACEUTICALS; PEGGY RYAN
    (E.D. Pa. Civ. No. 2-11-cv-07767)
    UNITED STATES OF AMERICA ex rel. MAX H. WEATHERSBY,
    JR.; MK LITIGATION PARTNERSHIP 2011, LLP
    v.
    ENDO PHARMACEUTICALS, INC.; ENDO PHARMACEUTICALS
    HOLDINGS, INC.; JAMES R. HAILEY; PEGGY RYAN
    (E.D. Pa. Civ. No. 2-10-cv-02039)
    UNITED STATES OF AMERICA ex rel. PEGGY RYAN
    v.
    ENDO PHARMACEUTICALS, INC.
    (E.D. Pa. Civ. No. 2-05-cv-03450)
    __________________________________
    On Appeal from the United States District Court
    for the Eastern District of Pennsylvania
    District Judge: Robert F. Kelly
    __________________________________
    Submitted on a Motion for Summary Affirmance
    Pursuant to Third Circuit LAR 27.4 and I.O.P. 10.6
    May 14, 2015
    Before: RENDELL, CHAGARES and SCIRICA, Circuit Judges
    (Filed: June 11, 2015)
    ________________
    OPINION*
    ________________
    PER CURIAM
    Gursheel Dhillon (“Dhillon”) appeals from an order of the District Court holding
    that Peggy Ryan is the sole Relator eligible to receive the settlement award, an order
    which effectively brought an end to his case. For the reasons that follow, we will
    summarily affirm.
    In February, 2011, Dhillon filed a False Claims Act (“FCA”) case against Endo
    Pharmaceuticals (“Endo”), alleging that Endo’s sales representatives promoted the off-
    label use of Lidoderm, which Dhillon learned about as a physician.1 Lidoderm is an
    adhesive patch and is approved only for the treatment of pain related to post-herpetic
    neuralgia, a complication of shingles. Thousands of ineligible Lidoderm prescriptions
    were submitted to Medicaid and Medicare for reimbursement. When Dhillon filed his
    *
    This disposition is not an opinion of the full Court and pursuant to I.O.P. 5.7 does not
    constitute binding precedent.
    1
    Because the parties are familiar with the background of this case, we only briefly
    summarize it here.
    2
    case, two other cases involving the off-label marketing of Lidoderm were already
    pending: Peggy Ryan’s case filed in 2005, U.S. ex rel. Ryan v. Endo Pharmaceuticals,
    Inc., D.C. Civ. No. 05-cv-03450, and Max Weathersby’s case filed in 2010, U.S. ex rel.
    Weathersby v. Endo Pharmaceuticals, Inc., D.C. Civ. No. 10-cv-02039. Ryan also filed
    an Amended Complaint -- on March 31, 2009 -- before either Weathersby or Dhillon
    initiated their actions.
    On February 21, 2014, the Government elected to intervene on behalf of the
    Relators for settlement purposes. On this same day, the Relators entered into a settlement
    agreement whereby Endo agreed to pay $171.9 million in exchange for being released
    from liability. The settlement expressly resolved the off-label FCA allegations of all
    three Relators. Dhillon was represented by counsel when he signed the settlement
    agreement and waived and forever discharged any claims against Endo for the covered
    conduct. The settlement agreement included a provision expressly reserving the issue of
    entitlement to a Relator’s share, which the District Court would decide. The Government
    took no position on this issue.
    Briefing ensued in the District Court, and Ryan requested that she be awarded the
    sole Relator’s share as the first-to-file. Dhillon argued that he was the first to state a
    plausible claim to relief and thus was entitled to a Relator’s share. He argued that,
    although Ryan’s Amended Complaint filed on March 31, 2009 was filed before his
    complaint, it failed to satisfy Federal Rule of Civil Procedure 9(b)’s particularity
    requirement; thus the first-to file rule was inapplicable. Ryan rebutted this argument, and
    also argued that Dhillon’s claims were precluded by the public disclosure bar. Dhillon
    3
    countered that the public disclosure bar was inapplicable because he qualified as an
    “original source.” Dhillon made certain additional arguments.
    In an order entered on June 23, 2014, the District Court granted Ryan’s motion,
    holding that she was the sole Relator eligible for the settlement award. The Court began
    with a first-to-file analysis, the threshold issue presented by the case, and determined that
    Ryan’s March 31, 2009 Amended Complaint was adequately pled in accordance with our
    recent decision in Foglia v. Renal Ventures Management, LLC, 
    754 F.3d 153
     (3d Cir.
    2014) (setting forth requisite pleading standard under Rule 9(b) for FCA claims). The
    Court remarked that the issue was not even close. Ryan not only set forth particular
    details of the scheme, but also supported them with solid evidence. The Court further
    determined that Dhillon failed to raise any off-label marketing claims that were unique
    from the claims raised by Ryan. Accordingly, Ryan was entitled to be awarded the sole
    Relator’s share as the first-to-file.
    The District Court then further held, in the alternative, that Ryan had correctly
    argued that Dhillon’s claims were precluded by the public disclosure bar. The Court
    noted that the Government produced a number of news articles, which originated prior to
    the filing of complaints by either Weathersby or Dhillon, and that these articles qualified
    as public disclosures from news media under the plain language of 
    31 U.S.C. § 3730
    (e)(4). The Court held that Weathersby’s and Dhillon’s qui tam actions were based
    upon the allegations set forth in the aforementioned public disclosures, and that they thus
    would have to be dismissed for lack of jurisdiction, 
    id.
     at § 3730(e)(4)(B), unless each
    Relator could show that he was an “original source.” The Court held that Dhillon had
    4
    failed utterly to show that he was an “original source” because he had no direct or
    independent knowledge of the fraud.2 The Court also rejected as meritless Dhillon’s
    other arguments based on the law of contracts, the statute of limitations, and the doctrine
    of laches.
    Dhillon filed a notice of appeal from the District Court’s June 23 Order, and then
    filed a timely motion for reconsideration. Ryan moved for an appellate bond of $25,000
    pursuant to Federal Rule of Appellate Procedure 7, arguing that it was necessary to
    ensure payment of costs on appeal. See Docket Entry No. 46, D.C. Civ. No. 05-cv-
    03450. The District Court, in an order entered on August 26, 2014, denied Dhillon’s
    motion for reconsideration. In a separate order entered on the same day, the Court
    ordered Dhillon to prepay an appellate bond in the amount of $10,000.
    We have jurisdiction under 
    28 U.S.C. § 1291
     and Federal Rule of Appellate
    Procedure 4(a)(4)(B)(i) to review the order entered on June 23, 2014 as to Dhillon,3 now
    that the District Court has denied his timely motion for reconsideration.4 Relator Ryan
    2
    By way of comparison, the District Court determined that Weathersby was an “original
    source.”
    3
    The District Court consolidated the three cases solely with regard to the issue of the
    Relators’ share of the settlement of federal claims relating to Endo’s off-label marketing
    conduct. Apparently, certain of Weathersby’s claims under analogous state laws remain
    pending in his case.
    4
    Dhillon did not file a new or amended notice of appeal within the time required once his
    motion for reconsideration was denied. The order denying the motion for reconsideration
    is the final order, but because Dhillon did not file a new or amended notice of appeal
    from it, we lack jurisdiction to review it to the extent that it decides new issues not
    decided by the District Court’s June 23 Order. Fed. R. App. Pro. 4(a)(4)(B)(ii);
    Carrascosa v. McGuire, 
    520 F.3d 249
    , 253-54 (3d Cir. 2008). We note also that Dhillon
    5
    has moved for summary affirmance under Third Cir. LAR 27.4 and I.O.P. 10.6, and, in a
    separate motion, has moved to dismiss or quash the appeal because Dhillon failed to pay
    the appellate bond. Dhillon has submitted written opposition to these motions and filed a
    pro se opening brief, which we will consider. In addition, Dhillon has moved to strike
    Ryan’s motions for summary affirmance and to dismiss or quash the appeal. Ryan has
    filed a motion to expedite disposition of her motions for summary affirmance and to
    dismiss or quash. The briefing schedule has been stayed and these motions are ripe for
    disposition. After the District Court denied his motion for reconsideration, Dhillon filed
    a Rule 60(b) motion in the District Court, alleging newly discovered evidence. See
    Docket Entry No. 60. The motion was stayed by the District Court pending the outcome
    of this appeal, see Venen v. Sweet, 
    758 F.2d 117
    , 120 (3d Cir. 1985). Dhillon has filed
    two motions in this Court, asking that we summarily remand the matter to the District
    Court for disposition of that Rule 60(b) motion. These motions also are ripe for
    disposition.
    We grant Ryan’s motion for summary affirmance and will summarily affirm the
    order of the District Court because no substantial question is presented by this appeal,
    Third Circuit LAR 27.4 and I.O.P. 10.6. Our review of matters of statutory interpretation
    is plenary. See U.S. ex rel. LaCorte v. SmithKline Beecham Clinical Labs., Inc., 
    149 F.3d 227
    , 232 (3d Cir. 1998). The False Claims Act (“FCA”) enables individuals, known
    filed a second motion for reconsideration, which the District Court denied. This second
    motion was untimely filed and did not toll the time for taking an appeal, Fed. R. App.
    Pro. 4(a)(4)(B)(i). Moreover, Dhillon did not separately appeal the order denying this
    second motion.
    6
    as Relators, to bring enforcement actions, known as qui tam actions, on behalf of the
    United States to recover funds which were fraudulently obtained, and to share in any
    resulting damages award. 
    31 U.S.C. § 3729
    , et seq. See also U.S. ex rel. Wilkins v.
    United Health Group, Inc., 
    659 F.3d 295
    , 304-05 (3d Cir. 2011). There are limitations to
    recovery, however. The first-to-file bar, for example, prohibits a Relator from bringing a
    case based on the same “essential facts” as an earlier-filed complaint, such that only the
    first-filed case may proceed to a damages award. 
    31 U.S.C. § 3730
    (b)(5); LaCorte, 149
    F.3d at 232-33 (if later filed allegation states all essential facts of previously-filed claim,
    section 3730(b)(5) bars later claim even if it incorporates somewhat different details).
    Only the first-filed Relator is entitled to a Relator’s share award from a settlement. Id.
    Cf. U.S. ex rel. Ortega v. Columbia Healthcare, Inc., 
    240 F.Supp.2d 8
    , 12 (D.D.C. 2003)
    (dividing the “bounty” has practical effect of reducing incentive to come forward with
    information on wrongdoing). The District Court held that the first-to-file rule applied to
    bar Dhillon’s claim for a share of the settlement.
    In his opening brief, Dhillon argues that once the Government intervenes, it cannot
    deny a Relator his statutory share of at least 15% under 
    31 U.S.C. §§ 3730
    (d)(1) and
    3730(c)(5). Appellant’s Informal Brief, at 11. In Rille v. PricewaterhouseCoopers LLP,
    
    748 F.3d 818
     (8th Cir. 2014), upon which Dhillon relies, the District Court awarded the
    Relators over $8 million. The Government, which had intervened and had adopted the
    Relators’ complaint, appealed and contended that the Relators were not entitled to any
    share of the recovery because their complaint did not state a plausible claim for relief.
    The Government contended that the claims it actually settled were unrelated to the
    7
    Relators’ action and therefore the settlement funds did not constitute “proceeds of the
    action or settlement of the claim” under § 3730(d)(1). The Court of Appeals for the
    Eighth Circuit sided with the Relators, holding that they were entitled to a 15% finder’s
    fee, so long as they were an “original source.” Rille, 748 F.3d at 825.
    In Dhillon’s case, the District Court decided -- adversely to him -- the threshold
    question whether his action was barred by the first-to-file rule. Accordingly, Rille, which
    does not concern the first-to-file issue, has no bearing on his case.5 Dhillon also argues
    that he must necessarily be an “original source” because, after he filed his “home run”
    complaint, Endo finally agreed to settle. Appellant’s Informal Brief, at 15. This
    argument is meritless; it again ignores the fact that the District Court decided the
    threshold first-to-file question adversely to Dhillon. Only the first-filed Relator is
    entitled to a Relator’s share award from a settlement, LaCorte, 149 F.3d at 232-33, and
    Dhillon is not a first-filed Relator. Although the first-to file issue is dispositive here, we
    note further that Dhillon’s complaint was indeed the last one filed before the claims were
    settled, but he provides no support for his argument that the temporal relationship
    between a qui tam complaint and a settlement has any bearing at all on the “original
    source” determination. He thus gives us no reason to overturn the District Court’s
    determination that he is not an “original source.”
    Dhillon next argues that Ryan’s March 31, 2009 Amended Complaint is itself
    subject to the first-to file and public disclosure rules because her original complaint
    5
    We further note that this opinion was vacated by the court and that rehearing en banc
    was granted. See Rille v. PricewaterhouseCoopers LLP, 
    2014 WL 5835459
     (8th Cir.
    August 27, 2014).
    8
    contained all of the required “essential facts.” Id. at 23. In U.S., ex rel. Shea v. Cellco
    Partnership, 
    748 F.3d 338
     (D.C. Cir. 2014), petition for cert. filed, upon which Dhillon
    relies, the Court of Appeals for the District of Columbia held that a Relator’s second
    action under the FCA was barred by the first-to-file rule because the second action
    incorporated the same material elements of fraud as his earlier-filed action, id. at 342-42.
    Shea does not apply here because Mr. Shea’s first qui tam action came to an end when
    the parties settled without admission of liability. Here, unlike Mr. Shea who filed a
    second qui tam action after his first action settled and came to an end, id. at 340, Ryan
    initiated only one qui tam action. Although an amended complaint supersedes an original
    complaint, as Dhillon argues, the filing of an amended complaint does not begin a new
    action; it is a continuation of the original action.
    Last, Dhillon argues that Ryan’s Amended Complaint did not comply with Rule
    9(b)’s heightened pleading requirements under the standard that applies in the Sixth
    Circuit Court of Appeals, see U.S. ex rel. Bledsoe v. Community Health Systems, Inc.,
    
    501 F.3d 493
    , 510 (6th Cir. 2007); that Sixth Circuit law should apply because he
    initiated his case in federal court in the Middle District of Tennessee; and that the District
    Court incorrectly applied Foglia. Appellant’s Informal Brief, at 27-28. We note that in
    Foglia we sided with those circuits that had used a “more nuanced” reading of the
    heightened pleading requirements of Rule 9(b) in deciding FCA cases, and that the Sixth
    Circuit Court of Appeals was not among those circuits.
    Dhillon’s case was originally filed in the Middle District of Tennessee but was
    transferred to the Eastern District of Pennsylvania where Ryan’s and Weathersby’s qui
    9
    tam actions already were pending. When a matter is not within the exclusive jurisdiction
    of a court, the law of the circuit in which the district court sits applies. See Pharmacia &
    Upjohn Co. v. Mylan Pharmaceuticals, Inc., 
    170 F.3d 1373
    , 1381 (Fed. Cir. 1999). The
    issue of Rule 9(b)’s particularity requirement is not a matter within the exclusive
    jurisdiction of any federal court, and, accordingly, Foglia applies to FCA cases decided in
    the Eastern District of Pennsylvania. The District Court properly reviewed Ryan’s March
    31, 2009 Amended Complaint under the test we adopted in Foglia, and correctly
    determined that Ryan amply complied with Rule 9(b). In Foglia, we held that a
    plaintiff’s claim must be accompanied by “particular details of a scheme to submit false
    claims paired with reliable indicia that lead to a strong inference that claims were actually
    submitted.” Id. at 157-58 (internal quotation marks removed). “Sufficient facts to
    establish ‘a plausible ground for relief’ must be alleged.” Id. at 158 (quoting Fowler v.
    UPMC Shadyside, 
    578 F.3d 203
    , 211 (3d Cir. 2009)).
    Ryan worked as a sales representative for Endo and assisted in the Government’s
    investigation, which began in 2005. In her Amended Complaint, she described a scheme
    undertaken by Endo to promote the off-label use of Lidoderm through the creation of
    fraudulent studies, by directing the sales force to advocate such applications, and by
    targeting and encouraging physicians through a system of kickbacks to prescribe the drug
    for such uses. She asserted that Endo touted the effectiveness of Lidoderm for off-label
    uses through supposedly independent studies, but these studies actually were financed
    and directed by Endo. She alleged that Endo directed company sales representatives to
    inform physicians of Lidoderm’s ability to treat carpal tunnel syndrome, osteoarthritis,
    10
    low back pain and other off-label conditions, and provided the representatives with
    literature and publications promoting Lidoderm’s off-label uses. She asserted that Endo
    used a system of kickbacks in order to encourage physicians to prescribe Lidoderm for
    unapproved uses. “High prescribers” were given honorariums to present at medical
    conferences and round table dinners. Finally, she used statistical sales data to further
    support her claim that Endo promoted the off-label use of Lidoderm. For instance,
    although the number of patients suffering from post-herpetic neuralgia has remained
    relatively constant, net sales of Lidoderm increased by 73% to $309.2 million in 2004.
    Since 2004, net sales of Lidoderm have more than doubled, and in 2007 reached $705.6
    million.
    Accordingly, Ryan’s Amended Complaint amply set forth “particular details of a
    scheme to submit false claims” and additionally supported them with evidence that would
    allow for a “strong inference” that false claims actually were submitted, Foglia, 754 F.3d
    at 156, thus satisfying Rule 9(b). Dhillon’s argument that Ryan’s Amended Complaint
    does not satisfy Rule 9(b)’s particularity requirement under the governing law is
    meritless.
    For the foregoing reasons, we grant Ryan’s motion and will summarily affirm the
    District Court’s June 23, 2014 Order. Ryan’s motion to expedite is granted. Ryan’s
    motion to dismiss or quash the appeal is denied as unnecessary. Dhillon’s motion to
    strike is denied. Dhillon’s two motions to summarily remand are denied as moot.
    11