Tanabe Seiyaku Co., Ltd. v. United States International Trade Commission

109 F.3d 726
CourtCourt of Appeals for the Federal Circuit
DecidedJune 6, 1997
Docket95-1448
StatusPublished
Cited by8 cases

This text of 109 F.3d 726 (Tanabe Seiyaku Co., Ltd. v. United States International Trade Commission) 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
Tanabe Seiyaku Co., Ltd. v. United States International Trade Commission, 109 F.3d 726 (Fed. Cir. 1997).

Opinion

109 F.3d 726

41 U.S.P.Q.2d 1976

TANABE SEIYAKU CO., LTD. and Marion Merrell Dow, Inc., Appellants,
v.
UNITED STATES INTERNATIONAL TRADE COMMISSION, Appellee,
and
Orion Corporation Fermion, Copely Pharmaceuticals, Inc.,
Interchem Corporation and Rhone-Poulenc Rorer,
Inc., Intervenors.

No. 95-1448.

United States Court of Appeals,
Federal Circuit.

March 7, 1997.
Rehearing Denied; Suggestion for Rehearing In Banc
Declined June 6, 1997.

S. Leslie Misrock, Pennie & Edmonds, New York City, argued, for appellants. With him on the brief were Marcia H. Sundeen, Washington, DC, and Joseph Diamante, New York City.

Cynthia P. Johnson, Attorney, Office of General Counsel, U.S. International Trade Commission, Washington, DC, argued, for appellee. With her on the brief were Lyn M. Schlitt, General Counsel, and James A. Toupin, Deputy General Counsel.

Richard D. Kelly, Oblon, Spivak, McClelland, Maier & Neustadt, P.C., Arlington, VA, argued, for intervenors. With him on the brief were Stephen G. Baxter and Martin M. Zoltick.

Before PLAGER, SCHALL and BRYSON, Circuit Judges.

PLAGER, Circuit Judge.

Tanabe Seiyaku Co., Ltd. and Marion Merrell Dow, Inc. (collectively "Tanabe") appeal from a final determination of the United States International Trade Commission ("Commission"), in In re Certain Diltiazem Hydrochloride & Diltiazem Preparations, No. 337-TA-349. Tanabe petitioned the Commission for a determination that the importation and sale of diltiazem by certain named respondents was a violation of United States law because the product was produced by a process that infringed a patent owned by Tanabe. The Commission denied the petition. Tanabe appealed to this court. We affirm the Commission's decision.

BACKGROUND

1.

Section 1337 prohibits "[t]he importation into the United States ... of articles that ... are made, produced, processed, or mined under, or by means of, a process covered by the claims of a valid and enforceable United States patent." 19 U.S.C. § 1337(a) (1994)1. Tanabe in its complaint to the Commission alleged that respondents by the importation, sale for importation, and sale within the United States of diltiazem hydrochloride and diltiazem preparations, produced by a process infringing claim 1 of United States Patent No. 4,438,035 (the " '035 patent"), were in violation of § 1337. The complaint sought an investigation by the Commission and, based on the investigation, issuance of a permanent exclusion order and permanent cease and desist orders. The complaint named ten respondents; this appeal concerns the Commission's determination as it applies to four of the respondents, Orion Corporation Fermion, Interchem Corporation, Copley Pharmaceuticals, Inc., and Rhone-Poulenc Rorer, Inc. (collectively "Fermion").

The Commission referred the matter to an administrative law judge ("ALJ") for an evidentiary hearing and initial determination. The proceedings were suspended during reexamination proceedings of the patent, requested by certain of the respondents. The suspension was lifted after the United States Patent and Trademark Office ("PTO") confirmed the patentability of all claims of the '035 patent, including claim 1, the only claim at issue.

The ALJ, following extensive pre-trial proceedings and a two-week hearing involving all parties, in an exhaustive 334-page opinion concluded that claim 1 was not infringed by any of the respondents, was invalid because it was obvious in view of the prior art, and was unenforceable due to inequitable conduct in its procurement.2 On certification to the Commission, the Commission affirmed the ALJ's disposition of the matter, albeit on narrower grounds than those recited by the ALJ.

The Commission limited its affirmance to the ALJ's interpretation of claim 1 and his consequent conclusion that the '035 patent was not infringed by any of the respondents. The Commission did not find it necessary to reach the issues of validity and enforceability, and took no position on those issues. Further, the Commission, by not reviewing them, caused the ALJ's findings in his initial determination regarding importation and the existence of a domestic industry to become a part of the Commission's final determination.

The '035 patent is a method or process patent. It discloses and claims a chemical process for preparing diltiazem hydrochloride, a pharmaceutical product used to treat various cardiovascular diseases, sold in dosage form by Tanabe under the name CARDIZEM TM. There was an earlier, now expired, patent on the product itself, diltiazem hydrochloride, United States Patent No. 3,562,257 (the " '257 patent"), also assigned to Tanabe. This product patent and its prosecution play a significant part in the Commission's interpretation of claim 1 of the '035 patent, as shall be explained below.

That claim, claim 1 of the '035 patent, reads:

1. A method of preparing a benzothiazepine derivative of the formula:

NOTE: OPINION CONTAINS TABLE OR OTHER DATA THAT IS NOT VIEWABLE

wherein R is a hydrogen or acetyl, or a pharmaceutically acceptable acid addition salt thereof, which comprises condensing a compound of the formula:

NOTE: OPINION CONTAINS TABLE OR OTHER DATA THAT IS NOT VIEWABLEwherein R is the same as defined above, with 2-(dimethylamino)ethyl halide either in the presence of potassium hydroxide in acetone or in the presence of potassium carbonate in a solvent selected from acetone, lower alkyl acetate, a mixture of acetone and water and a mixture of lower alkyl acetate and water, and if required, further converting the product into a pharmaceutically acceptable acid addition salt thereof.

(emphasis added).

The chemical reaction recited in claim 1 is known as an "N-alkylation" reaction. Compound II, the starting material for the N-alkylation reaction, is sometimes referred to as "TZP." At issue on appeal is the emphasized portion of the claim, which recites five combinations of "bases" and "solvents" used in performing the chemical reaction. The five base-solvent combinations disclosed in the '035 patent and recited in claim 1 are:

---------------------------------------------------------------
Combination  Base                 Solvent
---------------------------------------------------------------
     1       potassium hydroxide  acetone
     2       potassium carbonate  acetone
     3       potassium carbonate  acetone and water
     4       potassium carbonate  lower alkyl acetate
     5       potassium carbonate  lower alkyl acetate and water
---------------------------------------------------------------

The accused Fermion process involves performing the N-alkylation of TZP in the presence of the base potassium carbonate and, rather than acetone, the solvent butanone (also known as "methyl ethyl ketone" or "MEK") mixed with water.

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109 F.3d 726, Counsel Stack Legal Research, https://law.counselstack.com/opinion/tanabe-seiyaku-co-ltd-v-united-states-international-trade-commission-cafc-1997.