American Cyanamid v. Fermenta

Court of Appeals for the Third Circuit·Decided March 14, 1995·No. 94-5413·Unknown

Opinion

Opinions of the United

1995 Decisions States Court of Appeals for the Third Circuit

3-14-1995

American Cyanamid v Fermenta Precedential or Non-Precedential:

Docket 94-5413

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Recommended Citation "American Cyanamid v Fermenta" (1995). 1995 Decisions. Paper 73. http://digitalcommons.law.villanova.edu/thirdcircuit_1995/73

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UNITED STATES COURT OF APPEALS FOR THE THIRD CIRCUIT

N0. 94-5413

AMERICAN CYANAMID COMPANY, Appellant

v.

FERMENTA ANIMAL HEALTH COMPANY, a Delaware corporation

On Appeal From the United States District Court For the District of New Jersey (D.C. Civil Action No. 93-cv-04936)

Argued October 28, 1994

BEFORE: STAPLETON, HUTCHINSON and ROSENN, Circuit Judges (Opinion Filed March 14, 1995)

John Vanderstar (Argued)

Christopher N. Sipes

Covington & Burling

1201 Pennsylvania Ave., N.W.

P. O. Box 7566

Washington, D.C. 20044

and

Donald A. Robinson

Robinson, St. John & Wayne Two Penn Plaza East

Newark, N.J. 07105-2249

Of Counsel:

Ronald J. Cracas

Jane Y.C. Mathews

American Cyanamid Company One Cyanamid Plaza

Wayne, N.J. 07470-8426

Attorneys for Appellant

Clinton R. Batterton (Argued)

Edward John Allera

Naomi Joy Levan

Akin, Gump, Strauss, Hauer & Feld 1333 New Hampshire Ave., N.W.

Suite 400

Washington, D.C. 20036-1511

Of Counsel:

James B. Daniels

Friedman Siegelbaum

7 Becker Farm Road

Roseland, N.J. 07068

and

Lars H. Liebeler

The Robinson Law Firm

717 D Street, N.W., #400

Washington, D.C. 20004

Attorneys for Appellee

OPINION OF THE COURT

STAPLETON, Circuit Judge:

The issue in this case is whether a 1980 contract between the parties and a 1983 amendment thereto conveyed to American Cyanamid Company ("Cyanamid") perpetual rights to use the federal regulatory authority of Fermenta Animal Health Company ("Fermenta") to market an animal feed supplement. Cyanamid marketed the drug under the trademark Aureozol. Before the district court, both sides maintained that these documents are unambiguous, although each side differed on what was unambiguously stated therein. The district court held that "the plain language of the 1980 agreement and the 1983 amendment," when read against the background of the parties' pre-contract negotiations and post-contract conduct, did not convey that right. We will affirm.

I.

This dispute arises from a contract that was signed between Cyanamid, a chemical and pharmaceutical conglomerate, and Diamond Shamrock Corporation ("Diamond Shamrock") in 1980. Fermenta, the defendant in this case, became the successor in interest to Diamond Shamrock through an acquisition in 1985. The purpose of the contract was to enable Cyanamid to produce and sell an animal feed drug that Diamond Shamrock had developed and was marketing. The drug was an antibiotic animal feed supplement consisting of chlortetracycline, sulfathiazole, and penicillin, known as CSP 250. As consideration, Diamond Shamrock would receive an advance royalty and future royalties from Cyanamid's sales.

In order for Cyanamid to manufacture and sell Diamond's product, the contract granted it two distinct rights. First, Cyanamid was given access to Diamond Shamrock's proprietary information about its animal feed drug for the purpose of manufacturing and selling it. Equally important, the agreement gave Cyanamid the right to reference Diamond Shamrock's regulatory authority to sell the drug.

The FDA licenses the sale in interstate commerce of animal drugs by approving a manufacturer's New Animal Drug

Application (NADA), which remains on file with the FDA. Through the NADA, the FDA approves both the properties of the drug and its place and method of manufacture. See 21 U.S.C. § 360b(a). In 1971, Diamond Shamrock had obtained FDA approval for a NADA for its animal feed drug.1 Obtaining a NADA can be an expensive and lengthy process because of the amount of resources that must be expended on researching and demonstrating the safety and efficacy of the proposed animal drug. However, a company may be able to avoid the costs associated with obtaining its own NADA if it wishes to market a drug identical to that marketed by another company by requesting that company to allow it to reference the safety and efficacy data in its NADA. The current NADA holder must apply to the FDA for a "supplemental NADA" to enable the other company to reference its original NADA. See 21 C.F.R. § 514.8(a)(4)(v).2 Cyanamid entered into this contract with Diamond Shamrock because its own animal drug, which competed in the

1 . When Fermenta became the successor in interest to Diamond Shamrock's animal drug business, it acquired Diamond Shamrock's NADA authority, as noted in 21 C.F.R. § 558.15(g)(1). 2 . 21 C.F.R. § 514.8(a)(4)(v) provides in part:

A communication proposing a change in a new animal drug application should provide for any one of the following kinds of changes:

. . .

(v) Provision for outside firm to participate in the preparation, distribution, or packaging of a new animal drug (new distributor, packer, supplier, manufacturer, etc.).

market with Diamond Shamrock's CSP 250, was under scrutiny by the FDA for the possible carcinogenic effects of one of its components, sulfamethazine. Cyanamid sought to "insure" itself in the event the FDA took adverse action against its existing animal product by expanding its own product line to include Diamond Shamrock's animal feed supplement. Thus, in 1979, it entered negotiations with Diamond Shamrock, hoping to obtain the right to develop and sell Diamond Shamrock's product. Since Cyanamid could not sell Diamond Shamrock's drug without federal regulatory authority, the agreement required Diamond Shamrock to prepare and file a supplemental NADA establishing Cyanamid's facility as an alternate manufacturing site and designating Cyanamid as a distributor of the drug. In addition to pursuing an agreement with Diamond Shamrock, Cyanamid was formulating plans to obtain its own NADA for an animal product consisting of aureomycin, sulfathiazole and penicillin, a combination similar to CSP 250. This was reflected in a letter sent from Cyanamid to Diamond Shamrock during the course of negotiations in December of 1979.

Cyanamid and Diamond Shamrock executed their contract on July 23, 1980. Diamond Shamrock obtained the supplemental NADA in June of 1982 and the original five year contract period commenced on that date. Cyanamid thus enjoyed both commercial and regulatory rights to manufacture and sell the animal feed drug through June of 1987.

The contract also gave Cyanamid an option at the expiration of the agreement to purchase a perpetual license from

Diamond Shamrock. Article 9.2 provides in part:

Upon expiration of the full term of this Agreement . . . CYANAMID shall have the right to obtain a perpetual, paid-up, non-exclusive license, without right to sublicense, under TECHNICAL INFORMATION as shall have been licensed hereunder to CYANAMID upon the payment of twenty-five thousand ($25,000)

dollars to DIAMOND SHAMROCK for such perpetual rights.

App. 158.

The option described in Article 9.2 was exercised prematurely by the parties in 1983 in the form of an amendment to

the agreement. The amendment provides in part:

You will grant to us [Cyanamid] a perpetual paid-up nonexclusive license without right to sub-license under TECHNICAL INFORMATION as shall have been licensed under the Agreement upon our payment to you of $87,500 for such perpetual rights.

* * * *

All other terms and conditions of the Agreement will remain in effect.

App. 165.

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