In Re ROSENBERG

CourtCourt of Appeals for the Federal Circuit
DecidedJune 4, 2020
Docket19-2251
StatusUnpublished

This text of In Re ROSENBERG (In Re ROSENBERG) 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
In Re ROSENBERG, (Fed. Cir. 2020).

Opinion

Case: 19-2251 Document: 38 Page: 1 Filed: 06/04/2020

NOTE: This disposition is nonprecedential.

United States Court of Appeals for the Federal Circuit ______________________

IN RE: MICHAEL J. ROSENBERG, Appellant ______________________

2019-2251 ______________________

Appeal from the United States Patent and Trademark Office, Patent Trial and Appeal Board in No. 12/102,992. ______________________

Decided: June 4, 2020 ______________________

RONALD BRUCE GOLDSTEIN, Law Offices of Ronald B. Goldstein, North Brunswick, NJ, for appellant.

KAKOLI CAPRIHAN, Office of the Solicitor, United States Patent and Trademark Office, Alexandria, VA, for appellee Andrei Iancu. Also represented by THOMAS W. KRAUSE, AMY J. NELSON, FARHEENA YASMEEN RASHEED. ______________________

Before DYK, WALLACH, and CHEN, Circuit Judges. CHEN, Circuit Judge. Michael Rosenberg seeks review of a Patent Trial and Appeal Board (Board) decision affirming an examiner’s re- jection of claims 1, 3–9, 12–19, 21–27, and 30–36 of U.S. Case: 19-2251 Document: 38 Page: 2 Filed: 06/04/2020

2 IN RE: ROSENBERG

Patent Application No. 12/102,992 (the ’992 Application) under 35 U.S.C. § 101. We affirm. BACKGROUND The ’992 Application describes a method and system to collect performance-related data about a clinical trial, ana- lyze that data, and report on whether any adjustments should be made to the clinical trial based on the review of the collected data. As the specification explains with re- gards to this kind of performance review, “[t]he invention finds application in conducting clinical trials in the medical field, as well as in other management systems, by provid- ing a fully integrated ability to handle the many collection, analytic, and reporting functions.” J.A. 32. To avoid the lost time and cost of performing those collection, analytic, and reporting functions in person, the specification de- scribes performing them on a computer, in which data col- lected at remote sites is electronically transmitted to a central computer programmed to review the data to deter- mine whether any “procedures or parameters” used in the trial require modification. The collected data “comprise performance metrics,” which the specification describes as “benchmarks such as the number of queries generated by a clinical site, time to respond to queries, time to submit data following a patient visit, and other quality measures.” J.A. 39. Claim 1 is representative 1: l. A computer-implemented method for centrally managing data in an adaptive clinical trial or other adaptive process that is conducted at a plurality of geographically remote sites according to a set of procedures or parameters, said method comprising the steps of:

1 The government asserts that claim 1 is representa- tive, Appellee’s Br. at 4, and Mr. Rosenberg does not argue the substance of any limitations except for claim 1. Case: 19-2251 Document: 38 Page: 3 Filed: 06/04/2020

IN RE: ROSENBERG 3

(a) collecting data in the course of conducting said clinical trial or other process at a remote site, wherein the data comprise performance metrics with respect to said clinical trial or other process; (b) electronically transmitting the data from said remote site to a processing location; (c) checking the transmitted data at said pro- cessing location, in automated fashion, to assess the consistency of the data with respect to other col- lected data, to evaluate changes in the data as com- pared with data collected previously, or to monitor the data for trends over time; (d) electronically reporting the data to a pre-pro- grammed computer module; (e) determining, by use of said pre-programmed computer module, whether procedures or parame- ters utilized in conducting said clinical trial or other process require modification; and (f) providing instructions, based on said determin- ing, to follow or modify the procedures or parame- ters utilized in conducting said clinical trial or other process. J.A. 26. The examiner rejected all pending claims under the ab- stract idea exception of § 101 and the Board affirmed. Spe- cifically, the Board found claim 1 directed to a mental process, “specifically, evaluating data and rendering a judgment or opinion as to how the trial should or should not be modified based on the evaluation.” J.A. 19. In ad- dition, the Board found that claim 1’s reference to generi- cally-defined computer components (e.g., pre-programmed module) for performing the abstract process did not amount to an inventive concept. See J.A. 20–21, 357–59. Case: 19-2251 Document: 38 Page: 4 Filed: 06/04/2020

4 IN RE: ROSENBERG

Mr. Rosenberg appeals the Board’s decision. We have jurisdiction pursuant to 28 U.S.C. § 1295(a)(4)(A). DISCUSSION Section 101 allows inventors to obtain patents on “any new and useful process, machine, manufacture, or compo- sition of matter, or any new and useful improvement thereof.” § 101. However, “this provision contains an im- portant implicit exception”: an inventor may not patent laws of nature, natural phenomena, or abstract ideas. Al- ice Corp. Pty. Ltd. v. CLS Bank Int’l, 573 U.S. 208, 216 (2014). To assess whether a patent claim violates this ex- ception to the terms of § 101, the Supreme Court has set forth a two-step framework: (1) whether the claim is “di- rected to a patent-ineligible concept,” i.e., a law of nature, natural phenomenon, or abstract idea, and, if so, (2) whether the elements of the claim, considered “both indi- vidually and ‘as an ordered combination,’” add enough to “‘transform the nature of the claim’ into a patent-eligible application.” Id. at 217 (quoting Mayo Collaborative Servs. v. Prometheus Labs., Inc., 566 U.S. 66, 78 (2012)). Patent eligibility under § 101 is a question of law that may contain underlying issues of fact. Interval Licensing LLC v. AOL, Inc., 896 F.3d 1335, 1342 (Fed. Cir. 2018) (cit- ing Berkheimer v. HP Inc., 881 F.3d 1360, 1365 (Fed. Cir. 2018)). We review an ultimate conclusion on patent eligi- bility de novo. See id. I. ALICE STEP 1 The inquiry at this first stage looks at the “focus” of the claims, and their “character as a whole.” Enfish, LLC v. Microsoft Corp., 822 F.3d 1327, 1335–36 (Fed. Cir. 2016); Elec. Power Grp., LLC v. Alstom S.A., 830 F.3d 1350, 1353 (Fed. Cir. 2016). Representative claim 1 falls into a now- familiar class of claims directed to a patent-ineligible con- cept. In past cases, we have held claims focused on collect- ing and analyzing certain information and then reporting Case: 19-2251 Document: 38 Page: 5 Filed: 06/04/2020

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the results of that analysis are directed to an abstract idea. See e.g. Elec. Power Grp., 830 F.3d at 1353. In particular, “we have treated analyzing information by steps people go through in their minds, or by mathematical algorithms, without more, as essentially mental processes within the abstract-idea category.” Id. at 1354. We agree with the Board that Mr. Rosenberg’s claims are directed to the basic idea of deciding whether to fine- tune a given system (here, a clinical trial) based on review- ing the system’s performance data.

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In Re ROSENBERG, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-rosenberg-cafc-2020.