United States v. Sumitomo Pharma America, Inc.

CourtDistrict Court, D. Minnesota
DecidedSeptember 11, 2024
Docket0:17-cv-01719
StatusUnknown

This text of United States v. Sumitomo Pharma America, Inc. (United States v. Sumitomo Pharma America, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Minnesota primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United States v. Sumitomo Pharma America, Inc., (mnd 2024).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MINNESOTA

United States of America, ex rel. Scott File No. 17-cv-1719 (ECT/LIB) Louderback,

Plaintiff,

v. OPINION AND ORDER

Sumitomo Pharma America, Inc., formerly known as Sunovion Pharmaceuticals, Inc.,

Defendant. ________________________________________________________________________ Jeffrey J. Goulder and Michael Vincent, Stinson LLP, Phoenix, AZ, and Sharon Robin Markowitz, Stinson LLP, Minneapolis, MN, for Relator Scott Louderback. John P. Bueker and Sandra H. Masselink, Ropes & Gray LLP, Boston, MA, and Joseph T. Dixon, III, and Devin T. Driscoll, Fredrikson & Byron, P.A., Minneapolis, MN, for Defendant Sumitomo Pharma America, Inc., formerly known as Sunovion Pharmaceuticals, Inc. ________________________________________________________________________ Defendant Sunovion Pharmaceuticals1 manufactured a drug called Brovana. In this qui tam lawsuit brought under the federal False Claims Act, Relator Scott Louderback claims that Sunovion caused pharmacies to submit fraudulent claims for Brovana to Medicare.2 Louderback’s fraud theory proceeds in three steps: (1) he alleges

1 In January 2024, the parties stipulated to amend the case caption because Defendant Sunovion Pharmaceuticals, Inc., had changed its name to Sumitomo Pharma America, Inc. ECF No. 135. Notwithstanding the name change and caption amendment, Defendant in its briefing continued to refer to itself as “Sunovion.” See Mem. in Supp. [ECF No. 144] at 5 (ECF pagination). That convention will be followed here. 2 It seems plausible that pharmacies submitted Brovana claims to federal health-care programs in addition to Medicare. The operative Second Amended Complaint mentions only Medicare. See generally 2d Am. Compl. [ECF No. 128]. that Sunovion paid rebates to pharmacies in exchange for the pharmacies’ agreements to arrange for Medicare patients to receive Brovana prescriptions in situations where the patients would have received a different drug or therapy; (2) this rebates-for-prescriptions

arrangement violated the federal Anti-Kickback Statute; and (3) by law, a claim that includes items or services resulting from a violation of the Anti-Kickback Statute in turn violates the False Claims Act. Pursuant to Federal Rule of Civil Procedure 12(b)(6), Sunovion seeks dismissal of Louderback’s Second Amended Complaint. This is the case’s second round of Rule

12(b)(6) motions. In the first round, Sunovion’s Rule 12(b)(6) motion was granted, and the prior version of Louderback’s complaint was dismissed, because the pleading lacked allegations plausibly showing that false claims resulted from Sunovion’s assertedly illegal kickbacks. United States ex rel. Louderback v. Sunovion Pharms., Inc., 703 F. Supp. 3d 961, 977–980 (D. Minn. 2023); see United States ex rel. Cairns v. D.S.

Med. LLC, 42 F.4th 828, 834–37 (8th Cir. 2022) (interpreting “resulting from” in 18 U.S.C. § 1320a-7b(g) to require but-for causal relationship between kickback and claim). Louderback was given the opportunity to file an amended pleading, and Louderback filed the Second Amended Complaint. Sunovion’s motion will be granted. The Second Amended Complaint alleges facts

showing that pharmacies dispensed Brovana and received rebates. It does not take the necessary next step. That is, it does not plausibly allege that the rebates-for-prescriptions agreements caused pharmacies to dispense Brovana in any situation where, absent the agreements, a pharmacy or pharmacies would have dispensed a different drug or therapy. I

The Second Amended Complaint doesn’t change Louderback’s core factual allegations. To recap, Sunovion manufactures Brovana, a drug prescribed to treat chronic obstructive pulmonary disease. 2d Am. Compl. ¶¶ 36–37. Considering just pharmacies’ acquisition cost and Medicare’s reimbursement rate, pharmacies would lose money on Medicare-reimbursed Brovana prescriptions. Id. ¶¶ 57–60. Sunovion addressed this problem by paying rebates to pharmacies that signed a “Sunovion Part B Agreement.” Id. ¶ 68.3

Two provisions of the Part B Agreement remain essential to Louderback’s claims: what Louderback terms (1) the “dispense-as-written” provision and (2) the “counterdetailing” provision. According to Louderback, these two provisions require pharmacies to dispense Brovana as prescribed by physicians and prohibit pharmacies from educating prescribing physicians regarding less expensive equivalent or generic

alternatives to Brovana. Id. ¶¶ 76, 79. Based on these Part B Agreement provisions,

3 The First Amended Complaint attached the Part B Agreement as an exhibit. 1st Am. Compl. [ECF No. 92] ¶ 6 and at 38–49. Though Louderback expressly intended to attach it as an exhibit to the Second Amended Complaint, 2d Am. Compl. ¶ 6, he did not, see generally id. The Part B Agreement will nonetheless be considered in adjudicating Sunovion’s Rule 12(b)(6) motion. As a practical matter, Louderback clearly intended to attach the Part B Agreement to the Second Amended Complaint, and it seems safe to presume that its omission was just an oversight. As a legal matter, although it is true that an amended complaint supersedes all previous versions, exhibits attached to previous complaints may be considered if they are necessarily embraced by the operative amended complaint. See Vanderford v. Schnell, No. 22-cv-971 (DSD/DJF), 2023 WL 4489656, at *1 (D. Minn. July 12, 2023), R. & R. adopted, 2023 WL 4936159 (D. Minn. Aug. 2, 2023). Here, the Part B Agreement is embraced by the Second Amended Complaint because the Part B Agreement remains central to Louderback’s claims, it is cited several times, and its authenticity has not been questioned. See Zean v. Fairview Health Servs., 858 F.3d 520, 526 (8th Cir. 2017). Louderback alleges that Sunovion provides rebates “to pharmacies in exchange for their agreement to arrange for the prescription (by physicians), dispensing (by the pharmacists) and purchase (by patients and pharmacies) of Brovana in circumstances when, but for the

[Part B] Agreement, they would prescribe, dispense, or purchase drugs manufactured by Brovana’s competitors.” Id. ¶ 10.4 Louderback’s Second Amended Complaint adds several paragraphs directed toward causation. See id. ¶¶ 122–29. Louderback alleges “[Sunovion] sells Brovana at a wholesale price that exceeds the Medicare Maximum Price.” Id. ¶ 124(b). “Accordingly,

pharmacies cannot profitably offer Brovana to Medicare Part B beneficiaries unless they receive a rebate or discount on Brovana dispensed to those patients.” Id. ¶ 124(c). The owner of Deines Pharmacy, a pharmacy that signed a Part B Agreement, told Louderback that Deines Pharmacy could not afford to sell Brovana without the Part B Agreement’s rebate. Id. ¶ 125. The Second Amended Complaint includes eleven example instances

where Deines Pharmacy “sought—and received—reimbursement from Medicare Part B while the [Part B] Agreement was in effect.” Id. ¶¶ 110, 125(b).5 Louderback alleges

4 In the first Rule 12(b)(6) round, a theory based on a third “promotional services” provision was dismissed with prejudice. Louderback, 703 F. Supp. 3d at 980 n.7. Louderback did not remove allegations regarding this theory from the Second Amended Complaint. See, e.g., 2d Am. Compl. ¶¶ 3, 7, 71–72, 89–90, 92–93, 124, 146, 154, 160, and 177.

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