Maruho Co. v. Miles, Inc.

13 F.3d 6, 1993 U.S. App. LEXIS 33880, 1993 WL 530482
CourtCourt of Appeals for the First Circuit
DecidedDecember 29, 1993
Docket93-1385
StatusPublished
Cited by34 cases

This text of 13 F.3d 6 (Maruho Co. v. Miles, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the First Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Maruho Co. v. Miles, Inc., 13 F.3d 6, 1993 U.S. App. LEXIS 33880, 1993 WL 530482 (1st Cir. 1993).

Opinion

BREYER, Chief Judge.

Miles, Inc., invented and patented a pain-kihing drug called Xorphanol. In 1984, Miles gave Pars Pharmaceutical Co. the

exclusive right throughout the world to make, have made, use and sell

Xorphanol, in return for which Pars promised to pay a royalty and

to use reasonable efforts directly or through its subcontractors to develop one or more compounds ... to the point of [obtaining] ... government ... approval for ... [Xorphanol’s] therapeutic use....

In 1988, Pars subhcensed the plaintiff in this lawsuit, Maruho, Inc., to develop Xorphanol “compounds” and to sell them in Japan.

According to Maruho, Pars misled it during the sublicense negotiations. Although Maruho asked Pars to produce all relevant studies, Pars did not tell it about 1) an important negative study conducted by the *8 Charterhouse Research Unit of a well-known British pharmaceutical firm, Glaxo, Inc., and 2) a less important negative study conducted by the Director of the Stanford Pain Clinic. Both of these studies indicated that Xorpha-nol, while effectively reducing pain, also caused adverse side effects, such as headaches, drowsiness, dizziness, and euphoria. Maruho says that, had it seen these studies, it would not have bought the sublicense. In its view, Pars is guilty of fraud.

Maruho, however, seems unlikely to get its money back from Pars, for Pars is in the midst of bankruptcy proceedings. Maruho instead seeks recovery from Miles, Xorpha-nol’s original licensor; and, in this (diversity-based) lawsuit against Miles, it pleads various theories of state law. The district court, after examining the evidence proffered by the parties, granted summary judgment for Miles. Maruho appeals. We affirm the district court’s judgment.

I

Maruho’s Procedural Argument

At the outset, Maruho raises a procedural point. It says that the district court improperly converted a motion by Miles for judgment on the pleadings, Fed.R.Civ.P. 12(b)(6), into a motion for summary judgment, Fed.R.Civ.P. 56, without giving Maruho a “reasonable opportunity” to present “pertinent material.” See Fed.R.Civ.P. 12(b) (court shall treat motion for judgment on pleadings as a motion for summary judgment where “matters outside the pleading” are presented to and accepted by the court and “reasonable opportunity” to present “pertinent material” is “given”).

The record, however, does not support Ma-ruho’s claim. Miles’ motion gave Maruho adequate notice of the risk of summary judgment, for Miles entitled it “Motion to Dismiss or, in the Alternative, for Summary Judgment” (emphasis added). We concede that Maruho immediately told the court that it thought Miles’ motion requested summary judgment on only one count. But Maruho also told the court, in writing at the same time, that it would assume “that all of Miles’ contentions are asserted under both Fed. R.Civ.P. 12 and [summary judgment rule] 56” (emphasis in original). Maruho then presented to the court three volumes of documents, which it titled “Plaintiff Summary Judgment Record.” In response to questioning by this court at oral argument, Maruho could not identify any piece of evidence that it had lacked the opportunity to submit. Given these circumstances, Maruho converted Miles’ motion into a motion for summary judgment on all counts by presenting pertinent material outside the pleadings; and Ma-ruho not only had, but also took advantage of, a “reasonable opportunity” to present all “pertinent” material. See In re G. & A. Books, Inc., 770 F.2d 288, 294-95 (2d Cir.1985), ce rt. denied, 475 U.S. 1015, 106 S.Ct. 1195, 89 L.Ed.2d 310 (1986). The district court was therefore legally entitled to treat Miles’ motion as one for summary judgment on all counts.

II

Miles’ Participation in the Fraud

Maruho argues that Miles is liable as an actual participant in Pars’ fraud, either by “aiding and abetting” Pars’ fraud, by acting “in concert” with Pars, or by engaging in an “unfair or deceptive act or practice.” See Mass.Gen.L. ch. 93A, § 11; Kyte v. Philip Morris, Inc., 408 Mass. 162, 556 N.E.2d 1025 (1990); Restatement (Second) of Torts § 876(a), (b) (1979) [hereinafter “Restatement (2d) ”]. It says that, in the circumstances, a showing that Miles either 1) actually knew about the fraud, or 2) should have known about the fraud, is sufficient to trigger Miles’ liability as an actual participant. We shall consider, in turn, each of the two branches of Maruho’s argument.

1. Actual knowledge. We shall assume, for argument’s sake, that a finding that Miles actually knew about Pars’ fraud would trigger Miles’ liability. Nonetheless, like the district court, we do not believe the record would permit a reasonable juror to make that factual finding.

Maruho says that a juror might find Miles’ “actual knowledge” by inferring, from Miles’ conceded knowledge that Maruho was willing to pay $3 million for the sublicense, that *9 Miles must have known that Pars hid the negative Xorphanol studies from Maruho. Otherwise, why would Maruho pay so much for so little? To make the inference, however, requires some kind of propositional link, such as, “a knowledgeable firm would likely not have paid $3 million had it known about the studies.” The problem for Maruho is that this link is missing.

We agree with Maruho that a reasonable juror could believe that Miles knew the following:

a. After obtaining its license in 1984, Pars sublicensed Glaxo, Inc., a highly reputable British firm, to prepare Xorphanol for marketing. In 1986, Glaxo, after paying Pars more than $1.5 million for the sublicense, terminated the agreement.
b. Glaxo cancelled the sublicensing agreement after its Charterhouse Research Unit tested Xorphanol by giving ten volunteers single doses (each in an amount growing from 0.25 mg to 4.0 mg over the course of several days). The Charter-house study showed that many of these volunteers suffered some significant adverse side effect not suffered when they took a placebo.
c. Earlier, in 1985, the Director of Stanford Pain Clinic had conducted a multi-dose study of Xorphanol, giving volunteers several doses of 2 mg and 4 mg over several days.

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