In re Northfield Laboratories, Inc. Securities Litigation

267 F.R.D. 536, 76 Fed. R. Serv. 3d 1101, 2010 U.S. Dist. LEXIS 50292, 2010 WL 2011945
CourtDistrict Court, N.D. Illinois
DecidedMay 18, 2010
DocketNo. 06 C 1493
StatusPublished
Cited by5 cases

This text of 267 F.R.D. 536 (In re Northfield Laboratories, Inc. Securities Litigation) is published on Counsel Stack Legal Research, covering District Court, N.D. Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Northfield Laboratories, Inc. Securities Litigation, 267 F.R.D. 536, 76 Fed. R. Serv. 3d 1101, 2010 U.S. Dist. LEXIS 50292, 2010 WL 2011945 (N.D. Ill. 2010).

Opinion

MEMORANDUM OPINION AND ORDER

GEORGE M. MAROVICH, District Judge.

Lead plaintiffs, the Paul H. Shield, M.D. Inc. Money Purchase Plan and the Paul H. Shield, M.D. Inc. Profit Sharing Plan, together with named plaintiffs Alan Goodman, James Rourke and Daniel Nesi, assert two claims against defendants Northfield Laboratories, Inc. (“Northfield”), Steven A. Gould, M.D. (“Gould”) and Richard E. DeWoskin (“DeWoskin”). In Count I, plaintiffs assert that defendants violated § 10(b) of the Securities Exchange Act of 1934 (the “Act”), 15 U.S.C. § 78j(b), and Rule 10b-5, 17 C.F.R. § 240.10b-5. In Count II, plaintiffs assert against DeWoskin and Gould a “control person” claim for violation of § 20(a) of the Act. Lead plaintiffs and the named plaintiffs move for class certification.

I. Background

The Court has outlined the facts of this case in previous opinions. See In re: Northfield Labs., Inc. Securities Lit’n, 527 F.Supp.2d 769 (N.D.Ill.2007) and 2008 WL [540]*5404372743 (Sept. 23, 2008). The Court does not repeat the facts here.

Defendant Northfíeld was founded in 1985 by defendants DeWoskin and Gould. North-field’s primary purpose was to research and develop a hemoglobin-based blood substitute called PolyHeme to treat life-threatening blood loss. PolyHeme was a hemoglobin-based, oxygen-carrying blood substitute that was compatible with all blood types. North-field manufactured PolyHeme by extracting hemoglobin molecules from out human blood, chemically modifying the hemoglobin into a polymerized form of hemoglobin and incorporating the polymerized hemoglobin into a solution, which could then be administered to humans. Northfíeld was never able to bring PolyHeme to market, and the company declared bankruptcy on June 1, 2009. Defendant DeWoskin served as Chairman and CEO from 1985 to July 2002. Defendant Gould took over as Northfield’s Chairman and CEO in July 2002.

The Court previously concluded that plaintiffs had stated a claim against defendants for securities fraud. First, plaintiffs allege that after Northfíeld had closed a clinical trial due to allegedly negative results, defendants stated, on August 3, 2001, that they intended to close the trial. Second, plaintiffs allege that defendants, in Northfield’s August 9, 2002 10-K filing (and in its 2003 and 2004 10-K filings), misstated the reason why the clinical study was stopped. Third, plaintiffs allege that on October 11, 2001, Gould made a misstatement when he stated “no evidence of blood vessel constriction, or renal, pancreatic, gastrointestinal or cardiac dysfunction” were observed in a clinical trial even though cardiac dysfunction was observed. Fourth, plaintiffs allege that a September 4, 2001 press release contained misstatements about clinical trial results. Fifth, plaintiffs allege that defendants included misstatements in an August 3, 2001 proxy statement when they said “none of the adverse effects historically associated with other hemoglobin solutions have been identified by our clinical studies” when in fact, plaintiffs allege, cardiac events were not only present but historically associated with hemoglobin solutions.

II. Standard on a motion for class certification

As the parties proposing the class, the plaintiffs bear the burden of establishing that the putative class meets all of the requirements of Rule 23(a) and one of the requirements of Rule 23(b) of the Federal Rules of Civil Procedure. Oshana v. Coca-Cola Co., 472 F.3d 506, 513 (7th Cir.2006). Rule 23(a) allows individual plaintiffs to represent a class “only if: (1) the class is so numerous that joinder of all members is impracticable; (2) there are questions of law or fact common to the class; (3) the claims or defenses of the representative parties are typical of the claims or defenses of the class; and (4) the representative parties will fairly and adequately protect the interests of the class.” Fed.R.Civ.P. 23(a). The plaintiffs seek to proceed under Rule 23(b)(3), which allows a class action to proceed if “the court finds that the questions of law or fact common to class members predominate over any questions affecting only individual members, and that a class action is superior to other available methods for fairly and efficiently adjudicating the controversy.” Fed.R.Civ.P. 23(b)(3).

In Szabo v. Bridgeport Machines, Inc., the Seventh Circuit explained that a district court is not limited to the pleadings when considering a motion for class certification. The Seventh Circuit said:

Before deciding whether to allow a case to proceed as a class action, ... a judge should make whatever factual and legal inquiries are necessary under Rule 23. This would be plain enough if, for example, the plaintiff alleged that the class had 10,-000 members, making it too numerous to allow joinder, see Rule 23(a)(1), while the defendant insisted that the class contained only 10 members. A judge would not and could not accept the plaintiff’s assertion as conclusive; instead the judge would receive evidence (if only by affidavit) and resolve the disputes before deciding whether to certify the class.

Szabo, 249 F.3d 672, 676 (7th Cir.2001). Furthermore, the Seventh Circuit explained that if class certification issues overlap with [541]*541the merits, “then the judge must make a preliminary inquiry into the merits.” Id.

III. Discussion

Plaintiffs move to certify a class of:

all persons who purchased securities of Northfield Laboratories, Inc., including purchasers of common stock and call options, and sellers of put options, during the period from March 19, 2001, through March 20, 2006, inclusive.

Plaintiffs wish to exclude from the class “defendants, members of the immediate family of each of the defendants, any person, firm, trust, corporation, office, director, or other individual or entity in which any defendant has a controlling interest or which is related to or affiliated with any of the defendants, and the legal representatives, agents, affiliates, heirs, successors-in-interest or assigns of any excluded party.”

A. The Rule 23(a) requirements

1. Numerosity

Plaintiffs state that they do not know the number of class members but that the number is in the thousands. Defendants do not dispute this. Given that (1) Northfield had 14,242,000 shares outstanding at the beginning of the class period and 26,761,000 shares outstanding at the end of the class period; and (2) between 6.7% and 26.6% of the shares were held by institutional investors over the course of the proposed class period, the Court agrees that the number of class members is so high as to make joinder impracticable.

2. Common questions

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267 F.R.D. 536, 76 Fed. R. Serv. 3d 1101, 2010 U.S. Dist. LEXIS 50292, 2010 WL 2011945, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-northfield-laboratories-inc-securities-litigation-ilnd-2010.