In re Vicuron Pharmaceuticals, Inc. Securities Litigation

233 F.R.D. 421, 2006 WL 241472
District Court, E.D. Pennsylvania·Decided February 1, 2006·No. No. Civ.A. 04-2627·Published·Cited by 5 cases

Opinion

MEMORANDUM

BARTLE, District Judge.

Plaintiffs have sued defendants Vicuron Pharmaceuticals Inc. (“Vicuron”) and certain officers and directors in this consolidated putative class action for violations of the Securities and Exchange Act of 1934, as amended by the Private Securities Litigation Reform Act of 1995 (“PSLRA”), 15 U.S.C. §§ 78j(b) and 78t, and Rule 10b-5 promulgated thereunder, 17 C.F.R. § 240.10b-5. Before the court is the motion of Massachusetts State Carpenters Pension Fund (“MSCPF”), the Massachusetts State Guaranteed Annuity Fund (“MSGAF”), and the Greater Pennsylvania Carpenters Pension Fund (“GPCPF”), the named plaintiffs and proposed class representatives, for certification of a class comprising all purchasers of the securities of Vicuron between January 6, 2003 and May 24, 2004 and for appointment of class representatives and class counsel pursuant to Rule 23 of the Federal Rules of Civil Procedure.

I.

MSCPF, MSGAF, and GPCPF, which together are denominated the “Institutional Investor Group,” allege the following in support of their motion. See In re Vicuron Pharm., Inc. Sec. Litig., 225 F.R.D. 508 (E.D.Pa. 2004). In January, 2003, Vicuron completed the third phase of its trial of anidulafungin, a drug for the treatment of esophageal candidiasis (“EC”).1 At this time the two most favored drugs for treatment of EC were fluconazole and Caspofungin. The third phase of the anidulafungin trial apparently did not produce the results for which Vicuron had hoped. Within two weeks of treatment with anidulafungin, more than one-third of patients relapsed while only one-tenth of the patients treated with fluconazole and Caspofungin suffered such relapses. Nevertheless, on March 17, 2003, Vicuron stated that the third phase of the trial demonstrated that its drug was as effective as fluconazole. Vicuron announced on April 28, 2003 that it had submitted a new drug application (“NDA”) to the United States Food and Drug Administration (“FDA”) for approval of anidulafungin as a treatment of EC. In an accompanying press release, Vicuron asserted that its drug was as effective as fluconazole and that its NDA so stated.

Plaintiffs maintain that these misrepresentations by the defendants during the proposed class period (January 6, 2003 to May 24, 2004) regarding the efficacy of anidulafungin resulted in the artificial inflation of the value of Vicuron’s common stock to a high of $23.90 per share. According to the plaintiffs, this artificial increase allowed Vicuron to complete a merger with Biosearch Italia in March, 2003 by using 21.4 million shares of Vicuron stock to support the transaction. Vicuron was also able to complete a secondary offering of six million shares in July, 2003 for net proceeds of $83 million.

On May 24, 2004, Vicuron issued a press release acknowledging that the FDA had found its NDA for anidulafungin did not support the company’s proposed labeling for the product. While the press release disclosed that the FDA had serious concerns about how quickly EC reappeared in patients treated with anidulafungin as compared with fluconazole, it also stated that Vicuron’s NDA might eventually be approved with additional clinical data or studies. Upon the issuance of the press release, the value of Vicuron’s [425] stock sharply decreased to $13.04 per share, a loss of more than 40 percent from the previous day. The stock subsequently dropped to below $10.00 per share.

II.

The decision whether or not to certify a class lies within the court’s broad discretion exercised pursuant to Rule 23. See Battle v. Commonwealth of Pennsylvania, 629 F.2d 269 (3d Cir.1980); see also Robinson v. Metro-North Commuter R.R. Co., 267 F.3d 147 (2d Cir.2001); Gunnells v. Health-plan Services, 348 F.3d 417 (4th Cir.2003). In order to obtain certification of a class for trial or settlement, the party seeking the certification must satisfy the four threshold requirements of Rule 23(a): (1) numerosity, (2) commonality, (3) typicality, and (4) adequacy of representation. In addition to these requirements, the party moving for class certification must demonstrate that the action is maintainable under Rule 23(b)(1), (2), or (3). In re Warfarin Sodium Antitrust Litig., 391 F.3d 516, 527 (3d Cir.2004). Under Rule 23(b)(3), on which plaintiffs rely, two requirements must be met. First, common questions must “predominate over any questions affecting only individual members.” Second, class resolution must be “superior to other available methods for the fair and efficient adjudication of the controversy.” Id. Failure to satisfy any requirement precludes certification of the class. In Re LifeUSA Holding, Inc., 242 F.3d 136, 147 (3d Cir.2001). In this context, we are mindful of the fact that our Court of Appeals views the class action device as a “particularly appropriate and desirable means to resolve claims based on the securities laws, since the effectiveness of the securities laws may depend in large measure on the application of the class action device.” Yang v. Odom, 392 F.3d 97, 109 (3d Cir.2004) (internal citation omitted).

Vicuron does not dispute that the requirements under Rule 23(a) regarding numerosity, commonality, and typicality and those of predominance and superiority embodied in Rule 23(b)(3) have been met. Instead, Vicuron asserts that the MSCPF, MSGAF, and GPCPF would be inadequate class representatives under Rule 23(a)(4).2 Despite the lack of opposition to most of the motion for class certification, we must rigorously scrutinize the record to determine whether all the prerequisites of Rule 23(a) are satisfied as well as the predominance and superiority requirements of Rule 23(b)(3). See Gen. Tel. Co. of Southwest v. Falcon, 457 U.S. 147, 161, 102 S.Ct. 2364, 72 L.Ed.2d 740 (1982).

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In re Vicuron Pharmaceuticals, Inc. Securities Litigation, 233 F.R.D. 421, 2006 WL 241472 (E.D. Pa. 2006).

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