Federal Trade Commission v. Boehringer Ingelheim Pharmaceuticals, Inc.

241 F. Supp. 3d 91, 2017 WL 1030701, 2017 U.S. Dist. LEXIS 36816
CourtDistrict Court, District of Columbia
DecidedMarch 15, 2017
DocketMisc. No. 2009-0564
StatusPublished
Cited by1 cases

This text of 241 F. Supp. 3d 91 (Federal Trade Commission v. Boehringer Ingelheim Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Federal Trade Commission v. Boehringer Ingelheim Pharmaceuticals, Inc., 241 F. Supp. 3d 91, 2017 WL 1030701, 2017 U.S. Dist. LEXIS 36816 (D.D.C. 2017).

Opinion

MEMORANDUM OPINION

G. MICHAEL HARVEY, UNITED STATES MAGISTRATE JUDGE.

Over seven years ago, the. Federal Trade Commission (“FTC”) petitioned this *94 Court for an order instructing Boehringer Ingelheim Pharmaceuticals, Inc. (“Boeh-ringer”) to comply with a subpoena to produce documents for an ongoing FTC investigation. Following a decision from this Court, an appeal to and remand from the D.C. Circuit, and another decision from this Court consistent with the D.C. Circuit’s guidance, Boehringer now moves to stay the Court’s most recent Order “until all appeals, including any appeal to the United States Supreme Court, have been resolved.” Resp. Mot. [Dkt. 109] at 2. Boehringer’s Motion to Stay Production of Privileged Documents Pending Appeal is now ripe for adjudication. Based on a review of the relevant submissions 1 and for the reasons set out below, Boehringer’s motion for a stay is hereby DENIED.

BACKGROUND

The relevant facts underlying these proceedings are' more fully described in the Court’s prior- opinions and in the decision of the Court 'of Appeals. See FTC v. Boehringer Ingelheim Pharmaceuticals, Inc., 286 F.R.D. 101, 104-06 (D.D.C. 2012) (“Boehringer I”), aff'd in part, rev’d in part, and remanded, 778 F.3d 142 (D.C. Cir. 2015); FTC v. Boehringer Ingelheim Pharmaceuticals, Inc., 778 F.3d 142, 146-48 (D.C. Cir. 2015) (“Boehringer II”); FTC v. Boehringer Ingelheim Pharmaceuticals, Inc., 180 F.Supp.3d 1, 6-16 (D.D.C. 2016) (“Boehringer III”). The Court will provide only the important background information here.

A. Boehringer-Barr Litigation and the FTC Subpoena

The FTC filed this action to enforce an administrative subpoena duces tecum directed at Boehringer for an FTC investigation of a settlement agreement in a patent lawsuit between Boehringer and a generic drug manufacturer, Barr Laboratories (“Barr”). See Memorandum in Support of Petition to Enforce Subpoena [Dkt. 1-4] at 1-2. The FTC hopes to learn whether Boehringer and Barr violated antitrust laws. Id. In the subpoena, the FTC seeks documents from Boehringer relating to the patent litigation, the settlement of that litigation, and other agreements between Boehringer and Barr entered into at the time of settlement. Id. at 5-d3.

To summarize, Barr developed generic versions of two drugs that Boehringer manufactures, Aggrenox and Mirapex, and Boehringer sued Barr for patent infringement. S ee Boehringer Ingelheim Int’l GmbH v. Barr Labs., 562 F.Supp.2d 619, 622 (D. Del. 2008), rev’d 592 F.3d 1340 (Fed. Cir. 2010). After Boehringer lost at trial but won on appeal before the Federal Circuit, the parties agreed to settle the case and submitted their settlement to the FTC. See Boehringer I, 286 F.R.D. at 105. During the course of the lawsuit, Marla S. Persky, the Senior Vice President and General Counsel of Boehringer, helped advise her client on the settlement agreement. Id.

After the settlement, the FTC opened a formal investigation to determine whether Boehringer and Barr had engaged in unfair methods of competition through their settlement and other agreements. Id. The FTC was 'specifically concerned that Barr agreed to delay marketing its generic drugs, thereby giving Boehringer a mo *95 nopoly on profits for a time, in exchange for a payoff from Boehringer using those sales. Id. To aid in its investigation, the FTC served a subpoena on Boerhringer for documents concerning: (1) the patent litigation; (2) sales, profits, and marketing of the brand-name drugs; (3) the settlement agreement; (4) co-marketing with Barr and other firms; (5) Barr’s marketing of the generics; and (6) analyst reports on the drugs. Id.

B. Boehringer I and II

After Boehringer reported that it had fully complied with the subpoena, the FTC filed an objection, noting that Boehringer had withheld many relevant documents under claims of work-product protection and attorney-client privilege. Id. at 106. The FTC identified four categories of documents that it believes Boehringer improperly withheld: (1) financial analyses of a co-promotion agreement between Boeh-ringer and Barr regarding Aggrenox; (2) forecasting analyses of possible timelines for Barr’s generic drug to enter the market; (3) financial analyses of the business terms of the settlement agreement; and (4) notes taken by business executives. Id. at 108. The FTC argued that it had “an overriding and compelling need” for disclosure of these documents and that the attorney-client privilege did not apply to them because they were “business documents that'had no attorney as an author or recipient, or included an attorney only as part of a distribution to business executives.” Id. In response, Boehringer provided a sample set of documents for the Court to review in camera and also submitted in camera and ex parte affidavits from attorney Persky and attorney Pamela Taylor, who represents Boehringer in the FTC investigation. Id. at 109.

After examining those documents, this Court issued a decision sustaining'in part and overruling in part Boehringer’s assertions of privilege. With respect to the financial analyses of a co-promotion agreement between Boehringer and Barr on Aggrenox, forecasting analyses regarding Barr’s generic drug, and financial analyses used to evaluate the settlement agreement, the Court concluded that these documents were “an integral part of the litigation” and that information used to assess settlement options “clearly falls within the ambit of the work product doctrine.” Id. Further, the Court determined that these documents constituted opinion work product, which enjoys stricter protection than fact work product, and that the FTC could not discover them. Id. at 110. The Court also examined a number of emails, notes, and correspondence regarding strategic decisions and settlement options, concluding that they were protected as opinion work product. Id. Finally, the Court examined a number of emails reflecting requests for legal advice or conveying requests from attorneys for information to be used in settlement negotiations. Id. at 111. Though not protected by the work-product doctrine, the Court determined that these communications were shielded from disclosure by attorney-client privilege. Id.

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Bluebook (online)
241 F. Supp. 3d 91, 2017 WL 1030701, 2017 U.S. Dist. LEXIS 36816, Counsel Stack Legal Research, https://law.counselstack.com/opinion/federal-trade-commission-v-boehringer-ingelheim-pharmaceuticals-inc-dcd-2017.