Ballan v. Upjohn Co.

814 F. Supp. 1375, 1992 U.S. Dist. LEXIS 21279, 1992 WL 454968
CourtDistrict Court, W.D. Michigan
DecidedDecember 30, 1992
Docket1:92-cr-00009
StatusPublished
Cited by36 cases

This text of 814 F. Supp. 1375 (Ballan v. Upjohn Co.) is published on Counsel Stack Legal Research, covering District Court, W.D. Michigan primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Ballan v. Upjohn Co., 814 F. Supp. 1375, 1992 U.S. Dist. LEXIS 21279, 1992 WL 454968 (W.D. Mich. 1992).

Opinion

OPINION RE DEFENDANTS’ MOTION TO DISMISS

HILLMAN, Senior District Judge.

This class action asserts federal securities law violations against the various defendants — the Upjohn Company and its directors and executive officers. The class is yet to be certified. Before the court is defendants’ motion to dismiss for failure to state a claim under Rule 12(b)(6) and Rule 9(b) of the Federal Rules of Civil Procedure.

According to the complaint, defendants allegedly committed fraud on the stock market. Each of the individual defendants, by reason of his position as a director or executive officer of Upjohn, allegedly aided and abetted in the false and misleading statements issued by Upjohn. In Count I of the complaint, plaintiffs allege securities fraud pursuant to section 10(b) of the Securities Exchange Act of 1934, 15 U.S.C. 78j(b) and the *1378 Securities and Exchange Commission’s Rule 10b-5, 17 C.F.R. § 240.-10b-5.

Count II alleges a violation of § 20 of the Exchange Act. Count III alleges common law fraud and deceit.

The motion to dismiss has been fully and competently briefed. Oral argument was heard on October 26, 1992. The court has carefully considered all the arguments and authorities relied upon by all parties in then-briefs. For the reasons that follow, the motion to dismiss is denied with respect to all claims.

I. BACKGROUND

A. Allegations in the Amended Complaint

When considering a motion to dismiss, the factual allegations in the complaint must be construed as true. Jenkins v. McKeithen, 395 U.S. 411, 421-22, 89 S.Ct. 1843, 1848-49, 23 L.Ed.2d 404 (1969). What follows is a recitation of the allegations as made in the class action complaint.

Plaintiffs brought this case as a class action pursuant to Rule 23 of the Federal Rules of Civil Procedure, on behalf of themselves and all others who purchased Upjohn securities between January 21, 1989 and January 20, 1992. The amended class action complaint was filed on May 22,1992. The named plaintiffs allegedly purchased Upjohn’s common stock at prices that were inflated by the company’s misleading reports about Halcion and by defendants’ failure to disclose the side-effects of Halcion.

Defendant Upjohn is a Delaware corporation headquartered in Kalamazoo, Michigan. Upjohn researches, develops, produces, and sells prescription pharmaceuticals, and manufactures non-prescription drugs. Among the pharmaceuticals developed, manufactured, and marketed by Upjohn is the sleeping drug Halcion. Also named as defendants, in addition to Upjohn, are eight individuals who are identified as directors and/or officers of Upjohn. Defendant Dr. Theodore Cooper (“Cooper”) was at relevant times Chairman of the Board of Directors and Chief Executive Officer of Upjohn. He formerly was Vice-Chairman of the Board and, prior to that, Executive Vice-President. Defendant Mark Novitch (“Novitch”) was at relevant times a director of the Company. Novitch was elected Vice-Chairman of the Board of Directors in 1991. He had previously held the positions of Senior Vice-President for Scientific Administration and Vice-President and Executive Vice-President of the Company. Defendant Ley S. Smith (“Smith”) was a director of the Company. In 1991, he became Vice-Chairman of the Board of Directors. He previously served as Executive Vice-President of Upjohn. Defendant William U. Parfet (“W.U. Parfet”) served as a director and an Executive Vice-President, and Vice-President for Consumer Products, Healthcare Services and Pharmaceutical Strategic Planning, Vice-President and Treasure. He is currently President of the Company. Defendant Ray T. Parfet (“R.T. Par-fet”) served in the capacity of a director, and, before that, as Chairman and Chief Executive Officer of the Company. Defendant Lawrence C. Hoff (“Hoff’) was a director as well as, at various times, President, Chief Operating Officer and Executive Vice-President. Defendant R.C. Salisbury (“Salisbury”) was Senior Vice-President for Finance and Chief Financial Officer of the Company. Finally, Defendant Kenneth M. Cyrus (“Cyrus”) was Vice-President, Secretary and General Counsel of the Company. (Complaint at ¶¶ 8-15).

Upjohn began testing Halcion in clinical trials in the early 1970’s. It is marketed in more than 90 countries with annual sales of $250 million — $100 million in the United States. Halcion is also known as triazolam, a member of the benzodiazepine family, which includes Valium, Xanax, Dalmane and Resto-ril. (Complaint at ¶ 28). The plaintiff class is comprised of all persons who purchased Upjohn securities during the period from January 21, 1989, through January 20, 1992. Plaintiffs claim that defendants, pursuant to a common and continuous plan and scheme and conspiracy, and aiding and abetting one another, intentionally or recklessly concealed from regulatory agencies and the public material adverse facts about the side-effects of Halcion. (Complaint at ¶¶ 21, 26). As a result of defendants’ misrepresentations and omissions, plaintiffs allege that the market *1379 price of Upjohn securities was inflated to an artificially high level.

Plaintiffs also claim that defendants consistently touted the safety and effectiveness of Halcion despite defendants’ awareness of the problems experienced by persons who consumed Halcion. (Complaint at ¶ 27). In one of the earliest experimental tests of Halcion, Upjohn conducted Protocol 321 at Jackson Prison in Michigan in 1972. -When Upjohn submitted the testing results to the FDA and regulatory agencies in other countries, the company failed to include in the report the fact that almost 70% of the test subjects developed severe psychiatric reactions, including memory loss, depression and paranoia. (Complaint at ¶ 30).

Upjohn allegedly continued with the fraud and obtained approval in 1977 to market the drug in Belgium and the Netherlands at doses of up to 1 milligram. In 1979, the Netherlands, after having received approximately 1,100 reports from doctors citing serious side-effects in patients who took Halcion, banned the drug. At a later time, Upjohn convened a meeting in which twelve independent medical experts were asked to review the Dutch claims about the drug. These experts reported they could find no evidence to support the Dutch fears. The reason, according to the complaint, was that they were given only one doctor’s case reports. Plaintiffs allege that Upjohn made no mention of the well-documented reports to the panel of experts. (Complaint at ¶ 32-33).

In 1982, Halcion was licensed for sale in the United States for doses of up to 0.5 milligram. (Complaint at ¶¶ 32-34).

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Bluebook (online)
814 F. Supp. 1375, 1992 U.S. Dist. LEXIS 21279, 1992 WL 454968, Counsel Stack Legal Research, https://law.counselstack.com/opinion/ballan-v-upjohn-co-miwd-1992.