In re Bristol-Myers Squibb Securities Litigation

228 F.R.D. 221, 2005 U.S. Dist. LEXIS 15628, 2005 WL 1034129
CourtDistrict Court, D. New Jersey
DecidedApril 28, 2005
DocketNo. CIV.A. 00-1990SRC
StatusPublished
Cited by7 cases

This text of 228 F.R.D. 221 (In re Bristol-Myers Squibb Securities Litigation) is published on Counsel Stack Legal Research, covering District Court, D. New Jersey primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Bristol-Myers Squibb Securities Litigation, 228 F.R.D. 221, 2005 U.S. Dist. LEXIS 15628, 2005 WL 1034129 (D.N.J. 2005).

Opinion

MEMORANDUM OPINION

HUGHES, United States Magistrate Judge.

This matter comes before the Court upon Motion by Lead Plaintiff, the Long View Collective Investment Fund (“Plaintiff’), for leave to file a Third Amended Class Action Complaint. By way of background, Plaintiff originally sought to include certain newly-identified statements (“the statements”) in the “Contested Facts” section of the Joint [223]*223Final Pretrial Order (“FPO”). Defendants, Bristol-Myers Squibb Company (“BMS”) and individual Defendants Peter R. Dolan, Charles A. Heimbold, Jr. and Peter S. Ring-rose (collectively “Defendants”) opposed that proposal and the request was denied. Plaintiff subsequently filed the instant Motion for leave to amend the Complaint and Defendants submitted formal opposition to the Motion. The Court has reviewed the papers submitted by the parties and has decided the matter pursuant to Fed. R. Civ. P. 78. For the reasons stated below, Plaintiffs Motion to amend the Complaint is denied.

I. BACKGROUND AND PROCEDURAL HISTORY

In April of 2000, several class actions were filed against Bristol-Myers Squibb and its officers, alleging violations of federal securities law and state common law. The District Court consolidated the actions and appointed a Lead Plaintiff on July 24, 2000. A Consolidated Class Action Complaint was filed against Bristol-Myers Squibb, Heimbold and Ringrose and on March 8, 2001, after Defendants filed a motion to dismiss various claims, the Court upheld certain of Plaintiffs federal securities claims.

Subsequent to that Opinion, the District Court certified a class of all persons who purchased Bristol-Myers Squibb common stock during the time period spanning from November 8, 1999 through April 19, 2000 (“initial class period”). Following class certification, Plaintiffs were granted leave to file an Amended Complaint (“First Amended Complaint”) on or about May 15, 2002. This Complaint added allegations against Defendant Dolan, who had previously not been an individually named party to the case. Defendants were granted until October 21, 2002 to answer the First Amended Complaint. An Amended Answer was filed on or about November 13, 2002. On or about April 29, 2002, Defendants moved for Partial Judgment on the Pleadings, and on June 6, 2003, Plaintiff cross-moved for Leave to File a Second Amended Complaint.

In its proposed Second Amended Complaint, Plaintiff alleged violations of Section 10(b) of the 1934 Securities Exchange Act and Rule 10(b)(5) by all Defendants, as well as violations of 20(a) of the Exchange Act against Defendants Heimbold and Dolan. Additionally, on July 2, 2004, a Stipulation and Order was entered by the Court certifying a class of all persons who purchased Bristol-Myers Squibb common stock during the time period spanning from March 22, 2001 through March 20, 2002 (“second class period”). On August 19, 2004, the Court issued an Opinion granting and denying in part, Defendants’ Motion for Partial Judgment on the Pleadings and Plaintiffs Cross-Motions for leave to file a Second Amended Complaint.

Fact discovery in this matter closed on April 15, 2004, with the parties having engaged in wide-ranging fact discovery. Nearly four million pages of documents have been produced and a total of forty-four fact witnesses have been deposed. Additionally, the parties have submitted reports from twenty-six experts, and are currently conducting expert depositions. The parties have submitted a Proposed Final Pretrial Order and the Final Pretrial Conference began, but was aborted on December 15, 2004, due to the referencing of new statements here in issue. Finally, Defendants’ summary judgment motion was filed December 30, 2004 and is presently pending before the District Judge, together with various challenges to expert witnesses based upon Daubert v. Merrell Dow Pharmaceuticals, Inc., 509 U.S. 579, 113 S.Ct. 2786, 125 L.Ed.2d 469 (1993).

Briefly, the present Motion arises out of Plaintiffs efforts to include certain statements in the “Contested Facts” section of the proposed Joint Final Pretrial Order. That bid was denied and the issue now before this Court is whether these additional statements can be included as claims in an Amended Complaint and thereby be included in the Final Pretrial Order. Contrary to Plaintiffs assertion, the Court did not “order[] that Lead Plaintiff file this motion.” See PL [’s] Br. at 1. Rather, the Court simply denied Plaintiffs immediate request to insert the new statements and noted that they were entitled to make a formal motion. Thereafter, a motion was filed and the issue fully briefed by the parties.

[224]*224The statements, or newly-identified factual contentions, in dispute are contained in Plaintiffs “Contested Facts” section IV A(2) of the Proposed Final Pretrial Order submitted to the Court on December 14, 2004. Specifically, Plaintiff seeks to include the following:

The following representations of existing or historical facts made publicly by defendants BMS, Heimbold, Dolan, Ringrose and/or their agents on the dates indicated were false and/or misleading made:

November 8, 1999 (72nd Annual Scientific Session of the American Heart Association). Weber: “Just a quick look at safety and tolerability data. And there were no surprises here, and I’m not going to take up any real time looking at it.”

Weber: “And angioedema has been an issue with other drugs with ACE inhibition. There have been a lot of patients, as I mentioned earlier, who have already been exposed to Omapatrilat, including at this point over a thousand black patients, and the overall incidence of angioedema is .46 percent in the overall group, and 1.9 percent in black patients. There have been four patients who have had some airway compromise, that required some form of hospitalization or special treatment. There have been no deaths, and all patients have recovered completely. And just for comparison, these are experiences with benazepril, enalapril and lisinopril, three well known ACE inhibitors, showing that their incidence of angioedema is very similar to what we have found with omapatrilat, and given the closeness with which we are looking for these kinds of side effects, this would be very reassuring to me that there is, in fact, no difference.” Weber: “So, if I had to summarize what we’ve learned, so far, from our phase II and phase III studies, we find that the side effect profile is really very comparable to other ACE inhibitors; if we look at headache, if we look at cough. We already pointed out the obvious, you get more peripheral edema with amlodipine. There is no difference, again, no surprise here, between omapatrilat and placebo.” And, “[s]o we have a drug, Mr. Chairman, that has a unique mechanism of action that seems to translate into true clinical benefits. And it seems to be a safe and well tolerated drug with a profile very similar to current antihypertensive agents.”

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228 F.R.D. 221, 2005 U.S. Dist. LEXIS 15628, 2005 WL 1034129, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-bristol-myers-squibb-securities-litigation-njd-2005.