UNITED STATES оf America ex rel. Gursheel S. DHILLON, Appellant, v. ENDO PHARMACEUTICALS; Peggy Ryan. 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. United States of America ex rel. Peggy Ryan v. Endo Pharmaceuticals, Inc.
No. 14-3377.
United States Court of Appeals, Third Circuit.
Submitted May 14, 2015. Filed: June 11, 2015.
617 F. Appx. 208
Submitted on a Motion for Summary Affirmance Pursuant tо Third Circuit LAR 27.4 and I.O.P. 10.6 May 14, 2015.
Alan M. Freeman, Esq., W. Scott Simmer, Esq., Blank Rome, Washington, DC, Nicholas C. Harbist, Esq., Blank Rome, Princeton, NJ, Christopher C. Casper, Esq., John Newcomer, Esq., Elaine Stromgren, Esq., James, Hoyer, Newcomer & Smiljanich, Tampa, FL, for United States of America ex rel. Max H. Weathersby, Jr.; MK Litigation Partnership 2011, LLP.
Michael D. Granston, Esq., United States Department of Justice, Washington, DC, Margaret L. Hutchinson, Esq., Gerald B. Sullivan, Esq., Office of United States Attorney, Philadelphia, PA, for United States of America ex rel. Peggy Ryan.
Before: RENDELL, CHAGARES and SCIRICA, Circuit Judges.
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 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 а 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 for
Briefing ensued in the District Court, and Ryan requested that she be awarded thе 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
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
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 Wеathersby or Dhillon, and that these articles qualified as public disclosures from news media under the plain language of
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
We have jurisdiction under
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 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.
In his opening brief, Dhillon argues that once the Government intervenes, it cannot deny a Relator his statutory share of at least 15% under
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 sourсe.”
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 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
Last, Dhillon argues that Ryan‘s Amended Complaint did not comply with
Dhillon‘s case was originally filed in the Middle District of Tennessee but was transferred to the Eastern District оf Pennsylvania where Ryan‘s and Weathersby‘s qui 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
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 toutеd 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, 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” werе 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
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
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.
