Adair v. Carter

668 F.3d 1334, 101 U.S.P.Q. 2d (BNA) 1625, 2012 WL 372115, 2012 U.S. App. LEXIS 2388
CourtCourt of Appeals for the Federal Circuit
DecidedFebruary 7, 2012
Docket2011-1212
StatusPublished
Cited by3 cases

This text of 668 F.3d 1334 (Adair v. Carter) 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
Adair v. Carter, 668 F.3d 1334, 101 U.S.P.Q. 2d (BNA) 1625, 2012 WL 372115, 2012 U.S. App. LEXIS 2388 (Fed. Cir. 2012).

Opinion

LINN, Circuit Judge.

Appellants John Robert Adair, Diljeet Singh Athwal, and John Spencer Emtage (collectively, “Adair”) appeal a decision of the Board of Patent Appeals and Interferences (“Board”) holding that Adair’s single claim involved in Interference 105,744 with junior party Paul J. Carter and Leonard G. Presta (collectively, “Carter”) was barred under 35 U.S.C. § 135(b)(1). Because the Board properly determined that Adair’s claim was barred under § 135(b)(1), this court affirms.

I. Background

On November 21, 2005, Adair filed U.S. Application Serial No. 11/284,261 (“'261 Application”) with the United States Patent and Trademark Office (“PTO”). In a preliminary amendment filed concurrently with this application, Adair requested an interference based on Carter’s U.S. Patent No. 6,407,213 (“'213 Patent”). The only count of the interference is drawn to humanized antibodies. More specifically, the count involves non-human amino acid substitutions on specific residues of the heavy chain variable domain (an antibody comprises two light chains and two heavy chains, each with a “constant” and “variable” domain). On February 2, 2010, the Board declared the interference, identifying the claims in the count to be claims 30, 31, 60, 62, 63, 66, 67, 70, 73, 77-81 of the '213 Patent and claim 24 of the '261 Application. Carter v. Adair, Interference No. 105,744, Declaration of Interference at 4 (Feb. 2, 2010). The Board awarded Adair priority benefit to PCT/GB90/02017 (“PCT Application”), filed December 21, 1990, which claims priority to a British application filed by Adair on December 21, 1989.

Claim 66 of Carter’s '213 Patent, representative of the claims in the count and the basis for an interference-in-fact, recites:

66. A humanized antibody heavy chain variable domain comprising non-human Complementarity Determining Region (CDR) amino acid residues which bind antigen incorporated into a human antibody variable domain, and further comprising a Framework Region (FR) amino acid substitution at a site selected from the group consisting of: 24H [H=heavy], 73H, 76H, 78H, and 93H, utilizing the numbering system set forth in Kabat.

'213 Patent col. 881. 66-col. 89 1. 6.

Corresponding claim 24 in Adair’s '261 Application recites: *1336 '261 Application, Preliminary Amendment and Request for Interference dated Nov. 21, 2005 at 8, as amended, by Amendment of Sept. 9, 2009 at 4 (added language emphasized).

*1335 24. A humanised antibody comprising a heavy chain variable domain comprising non-human complementarity determining region amino acid residues which bind an antigen and a human framework region wherein said framework region comprises a non-human amino acid substitution at a residue selected from the group consisting of 23, 24, 49, 71, 73, and 78, and combinations thereof, as numbered according to Kabat.

*1336 Because Adair’s claim 24 was not presented to the PTO prior to June 18, 2003, one year from issuance of the Carter '213 Patent (the “critical date”) as required by 35 U.S.C. § 135(b)(1), Adair relied on precritical date claims 1 and 16 of the PCT Application and corresponding U.S. national stage Application No. 07/743,329 (“'329 Application”) to avoid the bar of § 135(b)(1). Claims 1 and 16 recite:

1. A CDR-grafted antibody heavy chain having a variable region domain comprising acceptor framework and donor antigen binding regions wherein the framework comprises donor residues at at least one of positions 6, 23 and/or 24, 48 and/or 49, 71 and/or 73, 75 and/or 76 and/or 78 and 88 and/or 91.
16. A CDR-grafted antibody heavy or light chain or molecule according to any one of the preceding claims comprising human acceptor residues and non-human donor residues.

PCT Application at 67-69. Adair originally relied on claim 8 of the PCT Application, but because that claim related to light chains, Adair later abandoned that argument. In its request for rehearing before the Board, Adair argued for the first time that claim 2 of the PCT Application also provided pre-critical date support for claim 24, but the Board declined to consider this argument for the first time on rehearing. Carter v. Adair, Interference No. 105,774, Decision on Request for Rehearing at 4-5 (Nov. 5, 2010) (“Rehearing ”).

At the national stage, the examiner originally rejected each of Adair’s PCT claims under one or more of the following sections: 101, 102(b), 103, and 112 first and second paragraphs. '329 Application, Office Action of November 18, 1992. Adair cancelled the PCT claims and added claims 23-66, later cancelled by an amendment adding claims 67-119 requiring multiple amino acid substitutions at specific locations in the heavy chain. '329 Application, Amendments of January 19, 1993 and April 16, 1993.

The Board rejected Adair’s argument that claims 1 and 16 in the PCT Application provide pre-critical date support for claim 24 in the '261 Application because: (1) the PCT claims were not patentable to Adair; (2) Adair added limitations to overcome the examiner’s rejection; and accordingly, (3) material differences presumptively existed between the post- and pre-critical date claims that Adair failed to rebut. Carter v. Adair, Interference No. 105,774, Decision on Motions at 9-10 (Aug. 30, 2010) (“Decision ”). Citing Regents of the University of California v. University of Iowa Research Foundation, 455 F.3d 1371, 1377 (Fed.Cir.2006), the Board stated that “[a]n applicant cannot expect to avoid the bar of § 135(b) by timely copying a claim from an issued patent when that claim is not patentable to that applicant.” Decision at 10-11. On rehearing, the Board rejected Adair’s assertion that materiality must be “determined in view of the patent claims being copied” and declined to compare Adair’s post- or precritical date claims with copied claim 66 from Carter’s '213 Patent. Rehearing at 3. Adair appeals, and this court has jurisdiction pursuant to 28 U.S.C. § 1295(a)(4)(A).

II. Discussion

A. Standard of Review

“We review the Board’s construction of 35 U.S.C. § 135(b)(1) de novo, as statutory interpretation is a question of law.” In re Berger, 279 F.3d 975, 980 (Fed.Cir.2002).

*1337 B. Analysis

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

Related

Speck v. Bates
Federal Circuit, 2024

Cite This Page — Counsel Stack

Bluebook (online)
668 F.3d 1334, 101 U.S.P.Q. 2d (BNA) 1625, 2012 WL 372115, 2012 U.S. App. LEXIS 2388, Counsel Stack Legal Research, https://law.counselstack.com/opinion/adair-v-carter-cafc-2012.