Yeda Research & Development Co. v. Abbott GmbH & Co. KG

837 F.3d 1341, 120 U.S.P.Q. 2d (BNA) 1299, 2016 U.S. App. LEXIS 17133, 2016 WL 5076060
CourtCourt of Appeals for the Federal Circuit
DecidedSeptember 20, 2016
Docket2015-1662; 2015-1663
StatusPublished
Cited by8 cases

This text of 837 F.3d 1341 (Yeda Research & Development Co. v. Abbott GmbH & Co. KG) 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
Yeda Research & Development Co. v. Abbott GmbH & Co. KG, 837 F.3d 1341, 120 U.S.P.Q. 2d (BNA) 1299, 2016 U.S. App. LEXIS 17133, 2016 WL 5076060 (Fed. Cir. 2016).

Opinion

REYNA, Circuit Judge.

Yeda Research and Development Co., Ltd. (‘Teda”) appeals two decisions by the United States District Court for the District of Columbia — one decided in 2008 (No. 2015-1663) and the other in 2015 (No. 2015-1662). Both district court decisions reviewed determinations by the Board of Patent Appeals and Interferences regarding Yeda’s assertion that Abbott GmbH & Co. KG’s (“Abbott”) U.S. Patent No. 5,344,915 (the “’915 patent”) is invalid as anticipated.

The ’915 patent’s invalidity turns on whether it benefits, from the filing dates from either of two German patent applications — P39 15 072 (the “’072 application”) and P39 22 089 (the “’089 application”). J.A. 5006. If it does, then the field of prior art narrows to exclude the anticipating reference. Whether the ’915 patent is entitled to benefit from the ’072 application’s filing date depends on whether the ’072 application provides adequate written description support for the invention claimed in the ’915 patent.

We affirm the district court’s 2015 decision that Abbott’s ’915 patent is supported by the written description of the ’072 application. As this renders moot Yeda’s appeal No. 2015-1663 concerning the district court’s 2008 decisión, we dismiss that appeal for want of jurisdiction.

BACKGROUND

A. Patented Technology

Abbott’s ’915 patent discloses a protein referred to as TBP-II. TBP-II binds to and neutralizes a protein called Tumor Necrosis Factor A (“TNFA”), which is associated with various immunological diseases. The ’915.patent has three claims. .’915 patent col. 6 11. 37-60. Claim 1 is representative:

1. A purified and isolated TNFA-bind-ing protein which has a molecular weight of about 42,000 dal-tons and has at the N terminus the amino acid sequence
Xaa Thr Pro Tyr Ala Pro Glu Pro Gly Set Thr Cys Arg Leu Arg Glu
where Xaa is hydrogen, a phenylalanine residue (Phe), or the amino acid sequences Ala Phe, Val Ala Phe, Gin Val Ala Phe, Ala Gin Val Ala Phe, Pro Ala Gin Val Ala Phe or Leu Pro Ala Gin Val Ala Phe.

The U.S. application that resulted in the ’915 patent was filed May 4, 1990. It claimed priority to two applications for a “novel protein” — the ’072 application, filed May 9, 1989, and the ’089 application, filed July 5,1989. J.A. 5006.

The prior art in question is the Engel-mann reference, which is an article pub? lished in January 1990 that describes and distinguishes the TBP-I and TBP-II proteins. 1 The parties do not dispute that Engelmann constitutes applicable prior art if the priority date for the ’915 patent is May 1990, but not if the ’915 patent benefits' from the filing date of either the ’072 or the ’089 application. The parties do not dispute that the Engelmann reference anticipates the ’915 patent if the priority date is May 1990.

*1344 Neither the ’072 nor the ’089 application discloses the full N-terminus sequence claimed in the ’915 patent. Instead, they disclose a partial N-terminus sequence, a protocol for obtaining the protein from its biological source, and additional properties of the protein, such as molecular weight, biological activity, and degradation characteristics when exposed to trypsin. The parties agree that the only protein containing the N-terminus sequence set forth in the ’072 application is TBP-II — i.e., the same protein claimed in the ’915 patent. J.A. 5024.

B. Procedural History

In 1996, the Board declared Interference No. 103,625 between Abbott’s ’915 patent and Yeda’s Application No. 07/930,-443. The Board assigned Abbott the May 1990 filing date of the application that became the ’916 patent and held that the ’915 patent was invalid as anticipated by Engelmann. Abbott filed suit in federal district court seeking review of the Board’s final decision. In 2008, the district court granted summary judgment for Abbott, holding that the ’089 patent inherently discloses the TBP-II protein and provides an adequate written description of the invention claimed in the ’915 application. The district court vacated the Board’s decision and remanded for further proceedings.

On remand, the Board reversed course. In 2010, the Board held that the ’072 application sufficiently disclosed TBP-II for the ’915 patent to benefit from the ’072 application’s May 1989 filing date. Yeda filed a district court action seeking review of the Board’s 2010 determination. In 2015, the district court affirmed the Board’s decision and granted Abbott summary judgment.

Yeda appeals the district court’s 2008 and 2015 decisions. We have jurisdiction over these appeals pursuant to 28 U.S.C. § 1295(a)(4)(C).

Standard of Review

This court reviews de novo a district court’s grant of summary judgment in an interference action. Boston Sci Scimed, Inc. v. Medtronic Vascular, Inc., 497 F.3d 1293, 1296 (Fed. Cir. 2007). We review de novo the district court’s legal determinations. See Rolls-Royce, PLC v. United Techs. Corp., 603 F.3d 1325, 1330 (Fed. Cir. 2010). The Board’s factual findings, including those relied on by the district court, are reviewed for substantial evidence. In re Gartside, 203 F.3d 1305, 1311-15 (Fed. Cir. 2000). Substantial evidence exists where a reasonable mind could accept it as adequate support for a conclusion. Id. at 1312 (citing Consol. Edison Co. v. NLRB, 305 U.S. 197, 229-30, 59 S.Ct. 206; 83 L.Ed. 126 (1938)).

Discussion

Yeda raises three arguments on appeal. First, Yeda challenges the legal standard applied by the district court to determine whether there was adequate written description support for the ’915 patent in the ’072 application. Second, Yeda argues that the prosecution history precludes Abbott from relying on inherent disclosure. Third, Yeda asserts that the district court erred in holding that the Board’s finding of adequate written description was supported by substantial evidence.

We first address the legal standard for written description support. In' order for the claims of the ’915 patent to benefit from the ’072 application’s filing date, the claimed invention'must be disclosed by the ’072 application. 35 U.S.C. §§ 112, 120; see Kennecott Corp. v. Kyocera Int’l, Inc., 835 F.2d 1419, 1421 (Fed. Cir. 1987).

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Cite This Page — Counsel Stack

Bluebook (online)
837 F.3d 1341, 120 U.S.P.Q. 2d (BNA) 1299, 2016 U.S. App. LEXIS 17133, 2016 WL 5076060, Counsel Stack Legal Research, https://law.counselstack.com/opinion/yeda-research-development-co-v-abbott-gmbh-co-kg-cafc-2016.