Takeda Pharmaceutical Co., Ltd. v. Dudas

511 F. Supp. 2d 81, 84 U.S.P.Q. 2d (BNA) 1365, 2007 U.S. Dist. LEXIS 70075, 2007 WL 2769687
CourtDistrict Court, District of Columbia
DecidedSeptember 18, 2007
DocketCiv. 06-1640 (TFH)
StatusPublished
Cited by6 cases

This text of 511 F. Supp. 2d 81 (Takeda Pharmaceutical Co., Ltd. v. Dudas) is published on Counsel Stack Legal Research, covering District Court, District of Columbia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Takeda Pharmaceutical Co., Ltd. v. Dudas, 511 F. Supp. 2d 81, 84 U.S.P.Q. 2d (BNA) 1365, 2007 U.S. Dist. LEXIS 70075, 2007 WL 2769687 (D.D.C. 2007).

Opinion

MEMORANDUM OPINION

THOMAS F. HOGAN, Chief Judge.

Pursuant to 35 U.S.C. § 145, Takeda Pharmaceutical Company (“Takeda”) challenges the Patent and Trademark Office (“PTO”) Board of Patent Appeals and Interferences’ (“Board”) reexamination rejection of Takeda’s patent covering a process to make certain cephem compounds. Pending before the Court are the parties’ motions for summary judgment. For the reasons that follow, the Court will grant Takeda’s motion and, accordingly, deny the PTO’s motion.

BACKGROUND

In 1974, Takeda filed a patent application in Japan covering, among other things, a new product (a “cephem” chemical compound) and processes for making the product. It then filed a similar application in Great Britain in 1975, again ap *84 plying for protection of cephem products and processes.

In December 1975, Takeda filed a patent application in the United States. Although describing seven processes to create cephem products, unlike the international applications, Takeda claimed only cephem products in its first United States patent application. In July 1988, U.S. Patent No. 4,098,888 (“'888 patent”) issued with 12 claims to cephem compounds.

In August 1979, Takeda filed a divisional application for 12 cephem compounds that differed slightly from those claimed in the '888 patent. The claims issued as U.S. Patent No. 4,298,606 (“'606 patent” or “product patent”).

On January 8, 1990, Takeda filed its first process claims relating to cephem compounds in the United States. Filing a preliminary amendment on April 3, 1990, Takeda presented 13 process claims for examination. The PTO initially rejected the process claims as obvious under 35 U.S.C. § 103. The Federal Circuit, however, reversed the PTO, see In re Ochiai, 71 F.3d 1565 (Fed.Cir.1995), and, on December 10, 1996, Takeda’s process claims issued as U.S. Patent No. 5,583,216 (“'216 patent” or “process patent”). Claim 1 of the '216 patent claims a specific manufacturing process for making certain cephem compounds claimed in the '606 patent. Pl.’s SOMF ¶ 15.

In 1998, E. Thomas Wheelock, Esq., on behalf of an anonymous requester, filed two requests for reexamination of the '216 patent. PL’s SOMF ¶ 7. Wheelock asserted that '216’s process claims were invalid for obviousness-type double patenting over the product claims of Takeda’s earlier patents, including the '606 patent. The PTO granted the requests and merged them into a consolidated reexamination proceeding. PL’s SOMF ¶ 7. On May 11, 2005, the patent examiner rejected the '216 patent as unpatentable based on double patenting. PL’s SOMF ¶ 8. Takeda timely appealed the examiner’s final decision to the Board.

In the Board’s view, Takeda’s appeal from the examiner’s denial “boil[ed] down to the following issue: Having taken out a full-term cephem compound patent (Ochiai 1 '606), are Appellants also entitled to take out yet another full-term patent to a method of making some of those cephem compounds where (1) the claimed method for making the cephem compounds is described in the cephem compound patent and (2) there is no credible alternative 2 method for making the cephems which does not involve an infringement of the method patent?” Board Op. at 13. Answering its own question, the Board stated, “We think not.” Id. After noting the two recognized categories of double patenting — i.e., “same invention” and “obviousness-type” — the Board rejected the “tendency to try to ‘pigeon hole’ every double patenting situation into one of these two recognized categories” and “decline[d] to hold that every double patenting must fit precisely into one of the two categories.” Board Op. at 14. Rather, the Board held, “the focus should be on whether the second patent unjustly extends the patent rights of a first patent.” Board Op. at 14. The Board then proceeded to affirm the examiner’s rejection of claims 1-5 of the '216 patent. Board Op. at 14-17.

*85 In the end, the Board concluded, “It should suffice to justify double patenting that some or all of the compound claims of an expired compound patent continue to be monopolized by virtue of patent rights in a narrow method patent.” Board Op. at 23-24. “[T]he focus” of double patenting, according to the Board, “should be on an analysis of whether all or some of a patentee’s patent rights are being unjustly extended.” Board Op. at 24. In Takeda’s case, the Board found that, “to the extent the Ochiai '216 patent extends the monopoly as to the compounds which can be made [only] by that process which are the same as the compounds covered by claim 1 of Ochiai '606, the monopoly of Ochiai '606 is also extended.” Board Op. at 24. Thus, the Board affirmed the examiner’s rejection of the '216 patent’s claims based on double patenting over certain claims of the expired '606 patent. Board Op. at 26.

Following the Board’s decision, Takeda timely filed suit in this Court, pursuant to 35 U.S.C. § 145, challenging the Board’s decision and requesting this Court hold that Takeda is entitled to a reexamination certifícate from the PTO confirming the patentability of claims 1-5 of the '216 patent. Compl. ¶ 18. Now pending before the Court are the parties’ motions for summary judgment. In its motion, Takeda argues it is entitled to judgment because (1) the Board’s decision rests on the erroneous factual finding that the '216 patent claims the only method of making the cephem compounds of claims 1 and 15 of the '606 patent, (2) the Board applied an incorrect legal standard for its double patenting rejection and, thus, its rejection is not in accordance with the law, and (3) the Board’s equitable arguments in support of its double patenting rejection are factually and legally incorrect. Pl.’s Mot. 6-7. The PTO opposes Takeda’s motion and cross moves for summary judgment, contending that substantial evidence supports the Board’s rejection of the '216 patent on the grounds of double patenting over the claims of the now-expired '606 patent.

DISCUSSION

I. LEGAL STANDARDS

A. Standard of Review

A dissatisfied patent applicant may challenge a Board decision by either appealing directly to the Federal Circuit, see 35 U.S.C. § 141, or by filing a civil action to obtain a patent in the United States District Court for the District of Columbia, see 35 U.S.C. § 145. Here, Takeda chose the latter route.

In pertinent part, § 145 provides: An applicant dissatisfied with the decision of the Board of Patent Appeals and Interferences in an appeal under section 134(a) of this title may ... have remedy by civil action against the Director in the United States District Court for the District of Columbia....

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511 F. Supp. 2d 81, 84 U.S.P.Q. 2d (BNA) 1365, 2007 U.S. Dist. LEXIS 70075, 2007 WL 2769687, Counsel Stack Legal Research, https://law.counselstack.com/opinion/takeda-pharmaceutical-co-ltd-v-dudas-dcd-2007.