Takeda Pharmaceutical Co., Ltd. v. Doll

561 F.3d 1372, 90 U.S.P.Q. 2d (BNA) 1496, 2009 U.S. App. LEXIS 7679, 2009 WL 961386
CourtCourt of Appeals for the Federal Circuit
DecidedApril 10, 2009
Docket2008-1131
StatusPublished
Cited by18 cases

This text of 561 F.3d 1372 (Takeda Pharmaceutical Co., Ltd. v. Doll) 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
Takeda Pharmaceutical Co., Ltd. v. Doll, 561 F.3d 1372, 90 U.S.P.Q. 2d (BNA) 1496, 2009 U.S. App. LEXIS 7679, 2009 WL 961386 (Fed. Cir. 2009).

Opinions

Opinion by the court filed by Circuit Judge RADER. Opinion concurring-in-part and dissenting-in-part filed by Circuit Judge SCHALL.

RADER, Circuit Judge.

The United States District Court for the District of Columbia held that later developments in the art may inform the “pat-entably distinct” determination for double patenting. Double patenting doctrines and case law permit this court to agree in part, but only to the extent that the subsequent developments predate the secondary application that triggers a double patenting rejection. Because genuine issues of fact cloud the date of availability of materially distinct processes, as well as the viability of those processes, this court vacates and remands.

I.

Takeda Pharmaceutical Co., Ltd. (Take-da) filed a patent application disclosing certain cephem compounds and the process for making those compounds in Japan on December 19, 1974. Takeda filed later applications in the United Kingdom on June 9, 1975, and in the United States on December 19, 1975. Takeda developed these new cephem compounds through an acylation process, introducing a new acyl group (RC=0) to an amino group (-NR3).

Takeda obtained a number of patents claiming these cephem compounds through a series of continuations, continuations-in-part, and divisional applications, including [1374]*1374the compound patents that issued as U.S. Patent No. 4,098,888 (the '888 product patent) (application filed Dec. 19,1975) and its divisional, U.S. Patent No. 4,298,606 (the '606 product patent) (application filed Aug. 28, 1979). This court refers to the December 19, 1975 application as the “primary application.” Takeda filed these applications before June 8, 1995, making them subject to the seventeen year patent term regime. See 35 U.S.C. § 154(c). In other words, the patent terms on these inventions began on their grant date, not on their filing date.

On January 8, 1990, Takeda filed its secondary application covering the process for making the cephem compounds claimed in the '888 and '606 product patents— sixteen years after the 1974 priority date, and more than fourteen years after the filing of the '888 product patent application. The process patent issued as U.S. Patent No. 5,583,216 (the '216 process patent) on December 10, 1996, claiming the sole process known and disclosed in the Japanese priority patent application. The '216 process patent led to the double patenting issue in this appeal.

In 1998, the United States Patent and Trademark Office (PTO) received two anonymous requests for reexamination of the '216 process patent. These requests asserted that the '216 process patent was invalid for “obviousness-type” double patenting in view of Takeda’s prior patents, as well as other prior art. During reexamination, Takeda relied upon the declaration of Dr. Wuest disclosing an alternative process (displacement process) for making the cephem compounds claimed in the '216 patent. Not persuaded by the Wuest declaration, the examiner rejected the '216 process patent claims as patentably indistinct over the '606 product patent claims. Takeda appealed the rejection to the Board of Patent Appeals and Interferences (the Board). The Board dismissed Dr. Wuest’s declaration as “speculative” and upheld the examiner’s double patenting rejection.

Takeda challenged the Board’s decision in the District Court for the District of Columbia under 35 U.S.C. § 145. Before the district court, Takeda presented new evidence in the form of a declaration of Dr. Duggan. In her declaration, Dr. Duggan explained that the process disclosed in U.S. Patent Nos. 6,552,186 (the Gerlach patent, published on Sept. 12, 2002, issued Apr. 22, 2003) and 7,071,329 (the Monguzzi patent, published June 2, 2005, issued July 4, 2006) provides a viable alternative, non-infringing process for making the certain cephem compounds claimed in the '606 product patent.

For purposes of cross-motions for summary judgment, the parties stipulated that “Method B” of the Duggan declaration described a materially distinct alternative process. Therefore, before the district court, the parties disputed whether the alternative process — Method B, developed after the date of invention — could defeat the double patenting rejection.

The district court concluded that “subsequent developments in the art [are relevant to] determining whether alternative processes exist” when weighing patentable distinctions for double patenting. Takeda Pharm. Co. v. Dudas, 511 F.Supp.2d 81, 91 (D.D.C.2007). Relying on Dr. Duggan’s disclosure of Method B (published in the Ger-lach and Monguzi patents in 2002 and 2005, respectively) the district court found that the product and process are “patent-ably distinct” and overturned the double patenting rejection. Id. at 92. The district court therefore granted Takeda’s motion for summary judgment that it was entitled to a reexamination certificate, confirming its right to the '216 patent. At the same time, the court denied the PTO’s motion for summary judgment. The PTO [1375]*1375timely filed a notice of appeal with this court.

II.

This court reviews a grant of summary judgment -without deference. Ethicon Endo-Surgery, Inc. v. U.S. Surgical Corp., 149 F.3d 1309, 1315 (Fed.Cir.1998). Summary judgment is appropriate if the record discloses no genuine issues of material fact. Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 247-48, 106 S.Ct. 2505, 91 L.Ed.2d 202 (1986). A material fact is one “that might affect the outcome of the suit under the governing law”; an issue is genuine “if the evidence is such that a reasonable [factfinder] could return a verdict for the nonmoving party.” Id. at 248, 106 S.Ct. 2505. This court reviews the Board’s factual findings for “substantial evidence.” Mazzari v. Rogan, 323 F.3d 1000, 1005 (Fed.Cir.2003). However, this court reviews the ultimate legal conclusion regarding double patenting without deference. In re Goodman, 11 F.3d 1046, 1050 (Fed.Cir.1993).

A.

Double patenting generally prevents a patentee from receiving two patents and extending the term of exclusivity for a single invention. See Perricone v. Medicis Pharm. Corp., 432 F.3d 1368, 1372 (Fed.Cir.2005). The proscription against double patenting takes two forms: statutory and non-statutory. Id. Statutory, or “same invention,” double patenting finds its origin in the statutory grant of “a patent” for any new and useful invention. 35 U.S.C. § 101; Perricone, 432 F.3d at 1372-73.

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Takeda Pharmaceutical Co., Ltd. v. Doll
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561 F.3d 1372, 90 U.S.P.Q. 2d (BNA) 1496, 2009 U.S. App. LEXIS 7679, 2009 WL 961386, Counsel Stack Legal Research, https://law.counselstack.com/opinion/takeda-pharmaceutical-co-ltd-v-doll-cafc-2009.