Freeman v. McKinnel

307 F. App'x 590
CourtCourt of Appeals for the Second Circuit
DecidedJanuary 27, 2009
DocketNo. 07-3547-cv
StatusPublished

This text of 307 F. App'x 590 (Freeman v. McKinnel) is published on Counsel Stack Legal Research, covering Court of Appeals for the Second Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Freeman v. McKinnel, 307 F. App'x 590 (2d Cir. 2009).

Opinion

SUMMARY ORDER

UPON DUE CONSIDERATION, IT IS HEREBY ORDERED, ADJUDGED and DECREED that the judgment of the district court be, and it hereby is, AFFIRMED.

Lead plaintiffs Marvin Freeman, Sanford Flinker,1 and Sylvia Flinker, who represent the plaintiff shareholders in related derivative suits against Pfizer, Inc. that were consolidated by the Panel for Multi[592]*592District litigation, appeal from a judgment against them based on an order of the United States District Court for the Southern District of New York granting the defendants’ motion to dismiss this action. We assume the parties’ familiarity with the facts and procedural history of this case, and the issues presented on this appeal.

The plaintiffs allege that the defendants, former directors and officers of Pfizer, were, or should have been, aware of significant cardiovascular risks associated with two of Pfizer’s highly successful Cox-2 inhibitor arthritis drugs, “Celebrex” and “Bextra,” and that they nonetheless permitted Pfizer to continue to market and sell these drugs aggressively, ultimately leading to hundreds of product liability or consumer fraud lawsuits and causing significant losses to Pfizer’s market capitalization. The plaintiffs filed a shareholder derivative suit against the defendants, proffering several theories of liability including breach of fiduciary duty, gross mismanagement, and waste of corporate assets. The district court dismissed the complaint pursuant to Federal Rule of Civil Procedure 23.1 on the ground that the plaintiffs had failed to make a demand on the Board of Directors of Pfizer (the “Board”) to initiate suit on behalf of the company, and had not pled facts sufficient to establish that such demand would be futile.

Rule 23.1(b) provides: “The complaint must ... state with particularity ... any effort by the plaintiff to obtain the desired action from the directors or comparable authority, and ... the reasons for not obtaining the action or not making the effort.” Fed.R.Civ.P. 23.1. The parties agree that since Pfizer is incorporated in Delaware, whether the demand requirement has been met is a question of Delaware law. See Scalisi v. Fund Asset Mgmt., L.P., 380 F.3d 133, 138 (2d Cir.2004).

We conclude that the alleged bases for demand futility are not sufficient to establish that there was a reasonable doubt that a majority of the Board “could have properly exercised its independent and disinterested business judgment in responding to a demand” at the time the complaint was filed allowing demand to be excused. Rales v. Blasband, 634 A.2d 927, 934 (Del.1993). We therefore affirm the judgment of the district court.

Plaintiffs A negations

In order to successfully plead demand futility, the plaintiffs must plead facts that, if proved, would demonstrate that a majority of board members, eight directors in this instance, were either not disinterested or lacked independence. The defendants concede that two defendants, McKinnell and Steere, are not disinterested. The plaintiffs must therefore successfully plead demand futility with regard to six other defendants in order to maintain this action. The plaintiffs have failed to do so.

“[T]he mere threat of personal liability ... is insufficient to challenge either the independence or disinterestedness of directors and ... a reasonable doubt that a majority of directors is incapable of considering demand should only be found where a substantial likelihood of personal liability exists.” Wood v. Baum, 953 A.2d 136, 141 n. 11 (Del.2008) (alteration in original) (internal quotation marks omitted). Where, as here, the defendant directors are contractually “exculpated from liability for certain conduct, then a serious threat of liability may only be found to exist if the plaintiff pleads a non-exculpated claim.” Id. at 141 (internal quotation marks and emphasis omitted).

Pfizer’s shareholders, pursuant to Del. Code. Ann. Tit. 8, § 102(b)(7) (2006), limited the directors’ liability to the full extent [593]*593permitted by Delaware Law. “Such a provision can exculpate directors from monetary liability for a breach of the duty of care, but not for conduct that is not in good faith or a breach of the duty of loyalty.” Stone ex Rel. AmSouth Bancorporation v. Ritter, 911 A.2d 362, 367 (Del.2006). This sets a higher threshold for the plaintiffs, because pleading a substantial likelihood of personal liability for a breach of good faith or the duty of loyalty requires the plaintiffs to allege different, and more culpable, conduct than necessary for a breach of the duty of due care. Id. at 369. We conclude that the plaintiffs allegations, do not meet that higher threshold. Presumption of Knowledge by the Defendants of the Results of Certain Studies

The plaintiffs’ allegations relating to personal liability each revolve around an asserted presumption that the defendant directors had knowledge of the drugs’ cardiovascular risks. The plaintiffs point to several sources where this knowledge would have come from. They cite a 1999 Pfizer internal clinical study on elderly Alzheimer’s patients that allegedly suggested heightened cardiovascular risks of Celebrex, and several published studies raising questions as to risks raised by Cox-2 inhibitors and calling for their assessment by drug companies. The plaintiffs also refer to lawsuits brought between 2001 and 2005 relating to the cardiovascular risks of Celebrex and Bextra. The plaintiffs would have the Court conclude on the basis of the defendant directors’ presumed knowledge of these studies that the defendant directors were “interested” directors because they were therefore aware of their substantial exposure to the risk of personal liability for a breach of their fiduciary duties. The plaintiffs argue that this knowledge should be presumed because it relates to a “core” activity of Pfizer, and courts have often presumed knowledge of information that relates to “core” activities of a corporation.

The plaintiffs have not cited any Delaware authority that would permit a court to infer from the existence of scientific studies within a corporation, without more, that the corporation’s directors had knowledge of their existence and import. There is no legal basis for a conclusion here that, amidst the innumerable studies that Pfizer would likely have conducted on innumerable subjects, the existence of one that may have found cardiovascular risks related to Celebrex was necessarily known by all members of the Board simply because it existed and was related to Pfizer’s “core” business. And without such an inference, the plaintiffs have alleged no facts that would lead to the conclusion that the defendants had such knowledge.

Nor have the plaintiffs established that defendants should be presumed to have known of published studies. In support of their proposition that knowledge of the studies should be presumed, the plaintiffs cite only one case that deals with demand futility under Delaware law, In re Biopure Corp. Derivative Litig.,

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

Related

Cite This Page — Counsel Stack

Bluebook (online)
307 F. App'x 590, Counsel Stack Legal Research, https://law.counselstack.com/opinion/freeman-v-mckinnel-ca2-2009.