Genex Corp. v. G.D. Searle & Co.

666 F. Supp. 755, 56 U.S.L.W. 2129, 1987 U.S. Dist. LEXIS 6959
CourtDistrict Court, D. Maryland
DecidedJuly 17, 1987
DocketCiv. JFM-85-4154
StatusPublished

This text of 666 F. Supp. 755 (Genex Corp. v. G.D. Searle & Co.) is published on Counsel Stack Legal Research, covering District Court, D. Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Genex Corp. v. G.D. Searle & Co., 666 F. Supp. 755, 56 U.S.L.W. 2129, 1987 U.S. Dist. LEXIS 6959 (D. Md. 1987).

Opinion

MEMORANDUM

MOTZ, District Judge.

Genex Corporation has brought this action against G.D. Searle & Co. and Searle Food Resources, Inc. alleging common law fraud and violations of the federal RICO, securities and antitrust laws. 1 Searle has counterclaimed for a double payment which it made to Genex on account. Discovery has now been completed, and Searle has moved for summary judgment as to all of the claims.

Background of the Controversy

Genex is a company involved in the research, development and manufacturing of biotechnological products. In approximately 1980 it devised a new process for manufacturing L-phenylalanine (“L-phe”), an amino acid. The principal commercial use of L-phe is in the production of aspartame, a low-calorie nutritive sweetener manufac *757 tured and marketed by Searle under the trade name“NutraSweet.” Searle holds the United States patent on the use of aspartame as a sweetener. The patent expires in 1992.

In July 1983 the FDA first approved the use of aspartame in carbonated beverages. As a result, a severe shortage of aspartame developed and, because of this shortage, Searle attempted to identify outside suppliers capable of producing L-phe. One of these suppliers was Genex, which in late 1980 had approached Searle with a proposal to supply aspartic acid, the other ingredient of aspartame.

Negotiations between Genex and Searle commenced in early 1983. These negotiations culminated in a license and supply agreement executed on August 14, 1983. The agreement was for a one-year period, called for the delivery of 50 tons of L-phe per month, gave Searle warrants to acquire 9.9% of Genex’s stock (at a price substantially above its market value) and granted Searle an exclusive 10-year license to Ge-nex’s L-phe technology and improvements thereto. ,

Statements allegedly made by Searle to Genex during the course of their contract negotiations lie at the heart of this suit. Genex contends (and for purposes of the present motion Searle admits) that Searle represented to Genex that “[1] it would make ‘some’ L-phe, but preferred to avoid, and did not plan, major back integration into L-phe production; [2] it would conduct a ‘horse-race’ among external L-phe manufacturers, evaluating short-term performance — measured by reliability of supply, quality and price — to determine which firms would supply its long-term L-phe needs; and [3] a long-term purchase arrangement would follow once Genex proved itself to be a capable and competitive L-phe supplier.” In fact, according to Genex, at the time these representations were being made Searle “was secretly embarked on a major program to make virtually all of its own L-phe by equipping and expanding an existing facility in Harbor Beach, Michigan, and by constructing on a ‘fast-track’ basis a large volume L-phe facility in Augusta, Georgia, to supply the total Lphe requirements for a new aspartame plant there.”

At the time that it entered into the August 1983 agreement, Genex did not have the manufacturing capacity to produce the L-phe which it was obligated to supply to Searle. Accordingly, in September 1983 it entered into a toll manufacturing agreement with Cell Products, Inc. under which Cell Products was to produce Lphe using the Genex process. However, in October 1983 Genex’s Board of Directors, drawing upon proceeds of a public offering which had been made in early 1983, approved the acquisition of a manufacturing plant in Pa-ducah, Kentucky, at which various products, including Lphe, were to be manufactured. In the preliminary prospectus for this stock offering, dated August 31, 1982, Genex had stated its intention to use 70-80% of the proceeds of the offering to “construct and equip additional laboratories and to obtain manufacturing facilities.”

During 1984 the parties conducted negotiations for a new contract extending beyond the August 1983 agreement. Although in late 1984 Searle issued a purchase order for 650 metric tons of L-phe from Genex to be delivered during the first ten months of 1985, no new omnibus agreement was ever executed. In June 1985 Searle informed Genex that it would not purchase any L-phe after October 1985 when deliveries under the purchase order were completed. This suit followed.

Fraud Claim 2

For the purpose of its summary judgment motion, Searle admits that it made *758 the misrepresentations which it is alleged to have made. The focus of its attack is upon Genex’s alleged reliance upon those misrepresentations and the reasonableness of that reliance. See, e.g., James v. Goldberg, 256 Md. 520, 261 A.2d 753, 758 (1970); Call Carl, Inc. v. BP Oil Corp., 554 F.2d 623, 629 (4th Cir.1977), cert. denied, 434 U.S. 923, 98 S.Ct. 400, 54 L.Ed.2d 280 (1977).

Proper analysis of Searle’s argument requires differentiation between two categories of damage claimed by Genex: (1) costs (in the amount of $1,506,054) which it incurred in commercializing and perfecting its L-phe manufacturing process during 1983; and (2) costs (in the amount of $18,279,409) which it incurred in purchasing, designing and equipping the Padu-cah plant. As to the former, although Ge-nex’s assertion that it incurred all of its 1983 L-phe research and development costs in reliance upon Searle’s alleged misrepresentations is suspect on its face, 3 genuine issues of material fact are presented which cannot be resolved short of trial. However, as to the Paducah plant claim, Searle’s motion will be granted since “the evidence is such that it ‘would require a directed verdict’ ” for Searle. See, e.g., Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 106 S.Ct. 2505, 2513, 91 L.Ed.2d 202 (1986); White v. Rockingham Radiologists, Ltd., 820 F.2d 98 (4th Cir.1987).

First, Genex’s proof of reliance does not establish its right to recover the full amount of its capital investment in the Paducah plant. The evidence is uncontra-dicted that Genex had adopted a corporate strategy to develop manufacturing capabilities (and publicly announced its plans to make a stock offering to implement that strategy) before Searle made any of its alleged misrepresentations. Thus, although it may be, as Genex alleges, that it would not have acquired the Paducah plant “but for” the misrepresentations, this is true only in the limited sense that the misrepresentations were the catalyst causing the acquisition decision to be made at the particular time that it was. Further, Jacques Delente, Genex’s executive vice president, testified on deposition that in making the Paducah acquisition, Genex was only counting on revenues from sales of L-phe to Searle for the short-term period that it would take Searle to develop the capacity to produce all of its own L-phe. On these facts Genex claims far too much in seeking to recover the full cost of the Paducah plant. 4

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Bluebook (online)
666 F. Supp. 755, 56 U.S.L.W. 2129, 1987 U.S. Dist. LEXIS 6959, Counsel Stack Legal Research, https://law.counselstack.com/opinion/genex-corp-v-gd-searle-co-mdd-1987.