Brunjes v. Hoyt

150 F.3d 153, 1998 U.S. App. LEXIS 15983
CourtCourt of Appeals for the Second Circuit
DecidedJuly 13, 1998
DocketDocket No. 97-7345
StatusPublished
Cited by1 cases

This text of 150 F.3d 153 (Brunjes v. Hoyt) 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
Brunjes v. Hoyt, 150 F.3d 153, 1998 U.S. App. LEXIS 15983 (2d Cir. 1998).

Opinion

WINTER, Chief Judge:

Joan T. Brunjes and Eugene Honeyman appeal from Judge Duffy’s dismissal pursuant to Fed.R.Civ.P. 12(b)(6) of their securities-fraud action. Their complaint alleged that Carter-Wallaee, Inc. violated Section 10(b) of the Securities Exchange Act of 1934, 15 U.S.C. § 78j(b), and Rule 10b-5,17 C.F.R. § 240.10b-5 (1971), by: (i) making materially false statements in the advertisements it ran in two medical journals, Neurology and Archives of Neurology, (ii) failing to disclose information that would correct misleading representations in its financial statements, and (iii) violating Generally Accepted Accounting Principles (“GAAP”). The district court held that, as a matter of law, Carter-Wallace’s advertisements in medical journals were not made “in connection with” a securities transaction and that the other omissions and statements identified in the complaint were not materially misleading. We do not agree that detailed drug advertisements in sophisticated medical journals can, as a matter of law, never be statements made “in connection with” a securities transaction. We affirm the dismissal of appellants’ other claims.

BACKGROUND

We of course accept the allegations of the complaint as true. See Jaghory v. New York State Dept. of Educ., 131 F.3d 326, 329 (2d Cir.1997). In July 1993, Felbatol, a new anti-epileptic drug produced by Carter-Wallaee was approved by the Food and Drug Administration (“FDA”) for sale as prescription medication. In August 1993, Carter-Wallaee [155]*155commenced selling Felbatol, hailing it as the first major anti-epileptic drug to be introduced in the United States in over fifteen years.

To promote Felbatol, Carter-Wallace ran a sixteen-page advertisement in the January 1994 issue of Neurology. The advertisement recited Felbatol’s safety record and stated that “no life-threatening liver toxicities or blood dyscrasias have been attributed to Fel-batol monotherapy.” An identical advertisement appeared in the January 1994 issue of Archives of Neurology. Five-page advertisements containing the same statement appeared in the February, March, April, May, June, and July 1994 issues of Neurology and Archives of Neurology.

During this period, Carter-Wallace issued other statements that are the subject of appellants’ complaint. Specifically, in June 1994, Carter-Wallace filed with the Securities Exchange Commission a Form 10-K in which it stated, pursuant to Section 13(a) of the Securities Exchange Act of 1934, 15 U.S.C. § 78m(a), that its sales were higher as a result of “greater than planned introductory sales of Felbatol.” In its annual “Report to Shareholders,” included in the Form 10-K, Carter-Wallace also represented that “Fel-batol sales have exceeded expectations,” that “[tjhis rate of growth is expected to continue,” and that the company expected “to receive royalties, which could be significant” from licensing Felbatol.

The present action concerns information received by Carter-Wallace in 1994 indicating that Felbatol caused, in some patients, a fatal form of acquired bone-marrow failure known as aplastic anemia. Carter-Wallace received the first report of a Felbatol-related aplastic-anemia death in January 1994. A report of another such death was received in March and reports of two deaths were received in each of April and May. On August 1, 1994, after four additional deaths were reported in July — amounting to a total of ten deaths — Carter-Wallace and the FDA issued a “Dear Doctors” letter, recommending that most patients be withdrawn from Felbatol treatment.

Appellants purchased shares of Carter-Wallace stock in June and July 1994. They allege that Carter-Wallaee’s advertisements in the medical journals were false and that its statements regarding Felbatol in the Form 10-K were misleading in the absence of disclosure of the reports of death due to aplastic anemia. They further allege that the advertisements and the Form 10-K misled the market and distorted the price of Carter-Wallace stock, thereby violating Section 10(b). In addition, appellants contend that Carter-Wallace violated GAAP, and, in turn, Section 10(b) by overstating the value of its Felbatol inventory when it knew the drug would not be commercially viable.

The district court dismissed the complaint under Rule 12(b)(6). With respect to appellants’ claims based on the advertisements in the medical journals, the district court found that the advertisements in stating that no reports of life-threatening effects had been received were false. See In re Carter-Wallace Sec. Litig., No. 94 Civ. 5704 (S.D.N.Y. Feb. 11, 1997). Nevertheless, it held that the advertisements were not actionable under Section 10(b) because, as a matter of law, drug advertisements in medical journals “[a]re not made in connection with the purchase or sale of securities, but [a]re directed at a technical audience intimately familiar with the potential adverse side effects of new drugs.” Id. With regard to appellants’ other claims, the district court held that Carter-Wallace’s representations in its Form 10-K and “Report to Shareholders” did not place the company under a duty to disclose prior to August 1, 1994, the Felbatol-associated deaths, because the company “justifiably went about accumulating more evidence regarding the possible adverse side effects in order to dissect the merits of the incoming reports.” Id.

DISCUSSION

We review de novo a district court’s dismissal of a complaint pursuant to Rule 12(b)(6). See Harsco Corp. v. Segui, 91 F.3d 337, 341 (2d Cir.1996). To state a claim under Section 10(b), “a plaintiff must plead that ‘in connection with the purchase or sale of securities, the defendant, acting with scienter, made a false material representa[156]*156tion or omitted to disclose material information and that plaintiffs reliance on defendant’s action caused [plaintiff] injury.’” In re Time Warner Inc. Sec. Litig., 9 F.3d 259, 264 (2d Cir.1993) (quoting Bloor v. Carro, Spanbock, Londin, Rodman & Fass, 754 F.2d 57, 61 (2d Cir.1985)). We turn now to the disputed issues concerning the advertisement in the medical journals and the statements in Carter-Wallace’s Form 10-K.

A. The Advertisements in Medical Journals

The crux of this issue involves whether Carter-Wallace’s Felbatol advertisements may constitute statements made “in connection with” a securities transaction, as required by Section 10(b). Appellants’ precise allegation is that Carter-Wallaee’s false advertisements in Neurology and Archives of Neurology “had an impact on the market price of Carter-Wallace common stock.”

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

Related

Cite This Page — Counsel Stack

Bluebook (online)
150 F.3d 153, 1998 U.S. App. LEXIS 15983, Counsel Stack Legal Research, https://law.counselstack.com/opinion/brunjes-v-hoyt-ca2-1998.