Schwarz Pharma, Inc. v. Paddock Laboratories, Inc.

504 F.3d 1371, 84 U.S.P.Q. 2d (BNA) 1900, 2007 U.S. App. LEXIS 23950, 2007 WL 2963935
CourtCourt of Appeals for the Federal Circuit
DecidedOctober 12, 2007
Docket2007-1074
StatusPublished
Cited by12 cases

This text of 504 F.3d 1371 (Schwarz Pharma, Inc. v. Paddock Laboratories, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Schwarz Pharma, Inc. v. Paddock Laboratories, Inc., 504 F.3d 1371, 84 U.S.P.Q. 2d (BNA) 1900, 2007 U.S. App. LEXIS 23950, 2007 WL 2963935 (Fed. Cir. 2007).

Opinion

LOURIE, Circuit Judge.

Schwarz Pharma, Inc. and Schwarz Pharma AG (collectively, “Schwarz”) appeal from the order of the United States District Court for the District of Minnesota entering summary judgment of nonin-fringement of U.S. Patent 4,743,450 (“the '450 patent”) in favor of Paddock Laboratories, Inc. (“Paddock”). Because the district court did not err in its conclusion that prosecution history estoppel bars resort to the doctrine of equivalents in this case, we affirm the entry of judgment of nonin-fringement.

BACKGROUND

Paddock filed Abbreviated New Drug Application 77-536 (“the ANDA”) at the Food and Drug Administration, pursuant to 21 U.S.C. § 355© (section 505© of the Federal Food, Drug, and Cosmetic Act), for approval to market generic tablets (“the Paddock drug”) containing moexipril hydrochloride (“MH”) and magnesium oxide (“MgO”). The ANDA certified, pursuant to 21 U.S.C. § 355®(2)(A)(vii)(IV), that the claims of the '450 patent are invalid and/or not infringed by the manufacture, use, or sale of the products for which approval was sought.

The '450 patent, issued on May 10,1988, is entitled “Stabilized Compositions” and relates to pharmaceutical compositions containing Angiotensin Converting Enzyme (“ACE”) inhibitors combined with stabilizers to prevent certain types of degradation. ACE inhibitors are prescribed for the treatment of hypertension (high blood pressure). Without the stabilizers, the ACE inhibitors may degrade through cyclization, discoloration (through oxidation), and hydrolysis. The '450 patent generally teaches use of an alkali or alkaline earth metal carbonate to inhibit cycli-zation and discoloration. The '450 patent expired on February 24, 2007.

Warner-Lambert Co., LLC (“Warner-Lambert”) owns the '450 patent, and Schwarz held an exclusive license under it with respect to the ACE inhibitor moexi-pril. MH is the hydrochloric acid salt of moexipril and the active ingredient in Schwarz’s Univasc® branded drug. Schwarz has alleged that Paddock infringed claims 1, 5-8, 12, and 16 of the '450 patent by filing the ANDA. Claims 1 and 16 are the only independent claims in the patent, and claim 1 of the patent reads as follows:

A pharmaceutical composition which contains:

(a) a drug component which comprises a suitable amount of an ACE inhibitor which is susceptible to cyclization, hydrolysis, and discoloration,
(b) a suitable amount of an alkali or alkaline earth metal carbonate to inhibit cyclization and discoloration, and
(c) a suitable amount of a saccharide to inhibit hydrolysis.

’450 patent col.5 1.57 — col.6 1.2 (emphasis added). Claim 16 of the '450 patent reads as follows:

A process for stabilizing an ACE inhibitor drug against cyclization which comprises the step of contacting the drug with:
(a) a suitable amount of an alkali or alkaline earth metal carbonate and,
(b) one or more saccharides.

Id. at col. 6 II. 54-59 (emphasis added).

Paddock filed a motion for summary judgment of noninfringement on June 30, 2006. The district court heard oral argument on the motion on August 30, 2006, and issued its Memorandum Opinion and Order granting the motion on October 20, *1373 2006. Schwarz stipulated at oral argument that the Paddock drug did not literally infringe the '450 patent, so the district court was only required to determine if there were genuine issues of material fact with respect to infringement under the doctrine of equivalents.

The district court determined as a matter of law that arguments made by the inventors and amendments to each of the independent clams in response to an obviousness rejection by the examiner during the prosecution of the application leading to the '450 patent did not result in argument-based estoppel, but did result in amendment-based estoppel. Originally, the independent claims recited a “metal containing stabilizer” and “an alkali or alkaline earth-metal salt,” respectively, but, following the rejection, each was amended to instead recite “an alkali or alkaline earth metal carbonate.” The court held that the change in claim language was a narrowing amendment and presumptively surrendered all metal containing stabilizers and alkali or alkaline earth metal salts except alkali and alkaline earth metal carbonates. The court also held that Schwarz had failed to rebut the presumption of surrender because magnesium oxide was a foreseeable equivalent of magnesium carbonate and because there was no objectively apparent reason for the narrowing amendment not directly related to the use of magnesium oxide. The court thus concluded that the Paddock drug could not infringe because Schwarz was estopped from claiming that the magnesium oxide used by Paddock was the equivalent of an alkali or alkaline earth metal carbonate.

In response to a motion to alter or amend the judgment, the district court issued a second Memorandum Opinion and Order on November 11, 2006, that affirmed its prior conclusion of noninfringement and explained its reasoning in even greater detail.

Schwarz timely appealed. We have jurisdiction pursuant to 28 U.S.C. § 1295(a)(1).

DISCUSSION

I. Jurisdiction

Paddock asserts as a preliminary matter that Schwarz lacks standing to bring this appeal because Warner-Lambert, the patent owner, did not appeal the district court’s adverse judgment. Paddock argues that Schwarz is merely an exclusive licensee of the '450 patent who does not possess “all substantial rights” in the patent, and Paddock joined Warner-Lambert in the suit in the district court as a matter of necessity. Paddock further argues that the same jurisdictional rule applies on appeal and that, without Warner-Lambert, Schwarz therefore lacks standing for its appeal. Paddock adds that it would be inappropriate for this court to permit join-der during the appeal to cure that defect because, although Warner-Lambert was a participant in the case below and well aware of its rights, it consciously chose not to appeal.

Schwarz responds that there is no need for Warner-Lambert to participate in the appeal for Schwarz to have standing to appeal. Schwarz notes that the requirement that an exclusive licensee join a patent owner in an infringement suit is a prudential rather than a constitutional one. Schwarz argues that it continues to have constitutional standing and that the purposes of the prudential standing requirement have already been served by the joinder of Warner-Lambert in the case below. Schwarz also states that if Warner-Lambert is a necessary party to the appeal, then its joinder can be ordered by this court.

*1374 Although we have stated the necessity of joining a patent owner in an action for infringement brought by an exclusive licensee a number of times,

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504 F.3d 1371, 84 U.S.P.Q. 2d (BNA) 1900, 2007 U.S. App. LEXIS 23950, 2007 WL 2963935, Counsel Stack Legal Research, https://law.counselstack.com/opinion/schwarz-pharma-inc-v-paddock-laboratories-inc-cafc-2007.