Taylor v. Bristol-Myers Squibb Company, Inc.

CourtDistrict Court, E.D. Kentucky
DecidedMay 26, 2020
Docket5:18-cv-00053
StatusUnknown

This text of Taylor v. Bristol-Myers Squibb Company, Inc. (Taylor v. Bristol-Myers Squibb Company, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. Kentucky primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Taylor v. Bristol-Myers Squibb Company, Inc., (E.D. Ky. 2020).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF KENTUCKY CENTRAL DIVISION LEXINGTON

) ) ) IN RE: ONGLYZA (SAXAGLIPTIN) ) MASTER FILE NO. 5:18-MD-2809-KKC AND KOMBIGLYZE XR ) (SAXAGLIPTIN AND METFORMIN) ) MDL DOCKET NO. 2809 PRODUCTS LIABILITY LITIGATION ) ) ALL CASES ) ) ) )

MEMORANDUM OPINION AND ORDER This matter comes before the undersigned pursuant to a referral from Judge Caldwell to handle the discovery disputes in this case. Defendants filed a Motion for Supplemental Protective Order. [DE 434]. Plaintiffs filed a Motion for Sanctions. [DE 456]. Both motions are fully briefed and ripe for a decision. The Court also held a telephonic conference during which the parties argued the merits of the Motion for Supplemental Protective Order. [DE 461]. As a result of those arguments, the Court requested additional briefing from both parties on the implications of international law on the documents the Defendants seek to protect with the Supplemental Protective Order. I. RELEVANT FACTUAL AND PROCEDURAL BACKGROUND This case is a multidistrict litigation arising from allegations that the Type 2 diabetes medication saxagliptin, sold under the brand names Onglyza and Kombliglyze XR, allegedly caused heart failure and/or increased the risk of adverse cardiac events. Defendants Bristol-Myers Squibb Company (“BMS”) and AstraZeneca (“AZ”) jointly studied, developed, and made submissions to the Food and Drug Administration (“FDA”). [DE 363 Page ID# 2205]. The District Court bifurcated discovery in this case to address general causation first. [DE 179]. The undersigned conducted a hearing on a discovery dispute on October 10, 2019. [DE 373 and 374]. As a result of this dispute the Court ultimately ordered Defendants to produce what the

parties have referred to as “the eCTD production” or “Module 5.” Essentially, this material is a broad range of studies and other information Defendants submitted to the Food and Drug Administration that relates to the drugs at issue in this case. The parties have generally referred to this as clinical trial data. At the time of the October 10, 2019, hearing, Defendants had produced some clinical trial data in TIFF format. Plaintiffs asked the Court to require Defendants to provide all clinical trials submitted to the FDA (about 150 trials) in native eCTD format, a request the Court granted. The Court granted this request for two reasons: (1) Defendants stated it would be relatively quick, inexpensive, and easy to produce the eCTD data, and (2) it became apparent at the hearing that the TIFF production of clinical trial data that had occurred up to that point was

missing critical metadata, rendering it essentially useless to Plaintiffs and their experts. The current dispute between the parties relates to the international clinical trial data contained in Module 5. Defendants have discovered that it will be timely and costly to redact data from Module 5, thus, they proposed producing all of the data but pursuant to a Supplemental Protective Order. The parties previously entered into a Stipulated Protective Order on October 2, 2018. II. ANALYSIS FED. R. CIV. P. 26(c) permits a court, “for good cause, issue an order to protect a party or person from annoyance, embarrassment, oppression, or undue burden or expense” including requiring that a trade secret or other confidential research, development, or commercial information not be revealed or be revealed only in a specified way[.]” FED. R. CIV. P. 26(c)(1)(g). “The burden of establishing good cause for a protective order rests with the movant. To show good cause, a movant for a protective order must articulate specific facts showing clearly defined and serious injury resulting from the discovery sought and cannot rely on mere conclusory statements.” Nix v. Sword, 11 Fed. App’x. 498, 500 (6th Cir. 2001) (citations and quotation marks omitted).

A. SUPPLEMENTAL PROTECTIVE ORDER IS NOT NECESSARY Here, Defendants do not seek to shield the Module 5 from discovery altogether, but instead seek a Supplemental Protective Order that greatly restricts access to and use of the materials. Yet, the Court finds the proposed Supplemental Protective Order is not necessary. Stated more precisely, the Court finds Defendants have failed to show that they will suffer serious injury or undue burden by proceeding under the existing Stipulated Protective Order. The parties jointly agreed upon a Stipulated Protective Order in this case that specifically resolves all of the concerns raised by Defendants in regard to Module 5. [DE 171]. The proposed Supplemental Protective Order is duplicative of many provisions in the Stipulated Protective Order and, thus, unnecessary. Even where the provisions that are not duplicative, the supplemental terms are so draconian that

they make any production of documents under the Supplemental Protective Order essentially useless. The examples best supporting this conclusion are as follows: 1. Attorney’s Eyes Only The existing Stipulated Protective Order sets forth mechanisms for designating documents Attorney’s Eyes Only (“AEO”). Specifically, the Stipulated Protective Order specifically notes that materials should be designated AEO (2) where the Confidential Discovery Materials contain private and/or PHI [Protected Health Information] of plaintiffs or persons not a party to the Litigation, including private and/or personal health, medical, employment, financial, and residence information; and (3) where documents originate from a jurisdiction outside the United States that (a) are subject to the protection of privacy and data protection[.] [DE 171 at Page ID # 850]. Plaintiffs all but admit that Module 5 likely contains information that would satisfy the requirements of the AEO designation in the Stipulated Protective Order. Thus, Defendants admit that they could use the Stipulated Protective Order to designate the entire Module 5 production as AEO. [DE 462 at Page ID # 3232]. Nevertheless, Defendants argue more is needed. Under the Stipulated Protective Order, Plaintiffs could challenge the AEO designation of any materials. The Supplemental Protective Order proposes designating the entire Module 5 production as AEO and demands that the entire production “will not be declassified,” essentially making the AEO designation of the entire Module 5 unchallengeable. [DE 434-1 at Page ID # 2900]. In fact, Defendants openly admit that the entire purpose behind the AEO provisions in the proposed Supplemental Protective Order is to circumvent the process by which Plaintiffs could challenge Defendants’ AEO designation of this production: “Given that Plaintiffs have indicated they may challenge Defendants’ position that clinical trial information constitutes Protected Health Information, however, it is important for

Defendants to have the propriety of the Attorneys’ Eyes Only designation determined prior to the production of the eCTD documents.” [DE 462, (emphasis in original)]. Defendants seek to designate the entire Module 5 as AEO, sight unseen, and have Plaintiffs forfeit their ability to challenge that designation on materials they have not reviewed. Defendants argue that producing this information without the oppressive provisions of the proposed Supplemental Protective Order means that they could be subject to penalty via international privacy law if Plaintiffs challenge the AEO designation and if the Court downgrades the designation. Ultimately, Defendants may be correct that this information is properly protected as AEO, but the process the parties, including Defendants, agreed upon in the Stipulated Protective Order should be allowed to play out.

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Medtronic Sofamor Danek, Inc. v. Michelson
229 F.R.D. 550 (W.D. Tennessee, 2003)

Cite This Page — Counsel Stack

Bluebook (online)
Taylor v. Bristol-Myers Squibb Company, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/taylor-v-bristol-myers-squibb-company-inc-kyed-2020.