In re Lifecore Biomedical, Inc. Securities Litigation

159 F.R.D. 513, 1993 U.S. Dist. LEXIS 20808, 1993 WL 761675
CourtDistrict Court, D. Minnesota
DecidedJune 14, 1993
DocketCiv. No. 4-92-955
StatusPublished
Cited by9 cases

This text of 159 F.R.D. 513 (In re Lifecore Biomedical, Inc. Securities Litigation) is published on Counsel Stack Legal Research, covering District Court, D. Minnesota primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Lifecore Biomedical, Inc. Securities Litigation, 159 F.R.D. 513, 1993 U.S. Dist. LEXIS 20808, 1993 WL 761675 (mnd 1993).

Opinion

ORDER

DOTY, District Judge.

This matter is before the court on defendants’ motion to dismiss plaintiffs’ Consolidated Amended Complaint pursuant to Rules 12(b)(6) and 9(b) of the Federal Rules of Procedure. Defendants also appeal from an order denying their motion to stay discovery entered by United States Magistrate Judge Floyd E. Boline, dated May 12, 1993. Based on the file, record and proceedings herein, and for the reasons stated below, the court holds that plaintiffs have failed to state a claim of securities fraud with sufficient particularity. The defendants’ appeal of Magistrate Judge Boline’s order is denied as moot.

BACKGROUND

Defendant James W. Bracke (“Bracke”) is the President, Chief Executive Officer and one of five directors of Lifecore Biomedical, Inc. (“Lifecore”), a Minnesota corporation. Lifecore develops, manufactures and markets sterile medical devices based on one of two natural biological materials, hyaluronate and hydroxylapatite. Hyaluronate is a water-retaining and lubricating carbohydrate that protects, cushions and moisturizes the body’s soft tissues.1 Lifecore has developed a method of producing purified hyaluronate which permits hyaluronate to be manufactured in large quantities. Currently, the primary application for Lifecore’s hyaluronate is as a component in ophthalmic surgical solutions.

This litigation concerns Lifecore’s Tenalure hyaluronate. Lifecore sells Tenalure to Ethicon, Inc. (“Ethicon”), a subsidiary of Johnson & Johnson, for testing in a soft tissue repair product intended to reduce post-surgical adhesions and scarring. Life-core supplies Tenalure to Ethicon pursuant to a February 1989 supply agreement. Ethicon has been conducting human clinical tests [515]*515since 1990.2 Before Ethicon can commercially sell a hyaluronate-based anti-adhesion product in the United States, it must receive marketing approval from the Food & Drug Administration (“FDA”).

On September 30, 1992, an Ethicon official stated that Ethicon was making efforts to develop alternatives to Lifecore supplying it with hyaluronate. The next day Bracke said there was no change in Lifecore’s relationship with Johnson & Johnson and that Life-core “was full steam ahead on preparing for this business.”

On Monday, October 5, 1992, Lifecore announced that it had been informed by Ethicon after the close of market Friday, October 2, 1992, that a “partial statistical analysis of data” from Ethicon’s human clinical testing of Tenalure “was not demonstrating anticipated levels of efficacy.” Lifecore stated that both companies were “continuing to confer regarding the future direction of the ongoing clinical evaluation.” Lifecore indicated that the companies had several options, “including further evaluation of the current hyaluronate product, bringing a second generation hyaluronate product to the clinic, or, discontinuing the project.” Bracke stated that he was “optimistic” that the companies could continue to collaborate on the clinical project, although the time frame for the project was “likely to be extended.”

On October 6, 1992, Bracke stated that the Tenalure test results probably would delay any marketing arrangement between Life-core and Ethicon. Lifecore announced on November 16, 1992, that Ethicon, after a thorough review of program options, “has indicated that it will continue its development project, based upon Lifeeore’s sodium hyaluronate technology, to create a product for reduction of surgical adhesions.” Lifecore stated that the “results of the clinical studies will be used to target new clinical evaluations to confirm the benefit of hyaluronate with a more significant level of activity.” Lifecore also announced that the two companies agreed to extend their 1989 supply agreement.

The original complaint charging the defendants with securities fraud, common law fraud and negligent misrepresentation was filed within hours of Lifecore’s announcement on October 5, 1992. Ten more class actions against defendants soon followed. Plaintiffs, purchasers of common stock of Lifecore between September 27, 1991, and October 5,1992, filed a Consolidated Amended Complaint on March 4, 1993. Plaintiffs allege, based largely on information and belief, that defendants committed securities fraud by making optimistic predictions regarding the status of Ethicon’s clinical testing of Tenalure and its ultimate marketability while concealing material information that made Tenalure’s future less rosy.

Based on the “close working relationship” between Lifecore and Ethicon, plaintiffs allege that defendants were aware of the status of Ethicon’s clinical testing of Tenalure or were reckless in not knowing such status given the importance of Ethicon to Lifeeore’s financial success. Plaintiffs contend that defendants concealed delays in the publicly announced timetable for the marketability of Tenalure. The complaint also alleges that by expressing continued optimism about the marketability of Tenalure, defendants led the investing public to believe that the ongoing clinical tests were proceeding without any problems when defendants knew or were reckless in disregarding that the tests were going poorly and that the results were in fact disappointing.

DISCUSSION

1. Failure to State a 10b-5 Claim

A motion to dismiss for failure to state a claim tests the sufficiency of the complaint. Scheuer v. Rhodes, 416 U.S. 232, 236, 94 S.Ct. 1683, 1686, 40 L.Ed.2d 90 (1974). When analyzing a motion to dismiss, the court looks to the complaint as pled. The complaint must be liberally construed and viewed in the light most favorable to the plaintiff. The court will dismiss a complaint for failure to state a claim only when it [516]*516appears the plaintiff cannot prove any set of facts that supports the claim. Conley v. Gibson, 355 U.S. 41, 45-46, 78 S.Ct. 99, 101-02, 2 L.Ed.2d 80 (1957).

Accepting the factual allegations of the complaint as true, the court cannot conclude at this time that plaintiffs can prove no set of facts which would entitle them to relief. Accordingly, the court denies defendants’ motion to dismiss plaintiffs’ complaint under Rule 12(b)(6).

2. Compliance with Federal Rule of Civil Procedure 9(b)

A claim for fraud under the federal securities laws, 15 U.S.C. § 78j(b), must be pled with particularity. Rule 9(b) provides that:

In all averments of fraud or mistake, the circumstances constituting fraud or mistake shall be stated with particularity. Malice, intent, knowledge and other condition of mind of a person may be averred generally.

While Rule 9(b) permits averment of knowledge and intent in general terms, it also mandates that a complaint plead the circumstances constituting fraud with particularity.

The United States Court of Appeals for the Eighth Circuit has not indicated exactly how Rule 9(b) applies in the securities fraud context. The Second Circuit has strictly applied Rule 9(b) to claims of fraud under the federal securities laws as a means of deterring frivolous suits.

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159 F.R.D. 513, 1993 U.S. Dist. LEXIS 20808, 1993 WL 761675, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-lifecore-biomedical-inc-securities-litigation-mnd-1993.