Patentee’s Own Clinical Trial Renders Unpatentable Patent Claims Directed to Antibody Treatment

October 9, 2023

Reading Time : 3 min

In a final written decision of an inter partes review proceeding, the Patent Trial and Appeal Board found all 12 claims of a challenged patent unpatentable as either anticipated or obvious. Each ground of unpatentability relied, in whole or in part, on Patent Owner’s own prior art, including clinical trials published at ClinicalTrials.gov.

The challenged patent was directed to methods of treating rheumatoid arthritis comprising administering a fixed dose of tocilizumab, an antibody that binds to the receptor of interleukin-6. Petitioner asserted that the challenged claims were anticipated by a clinical trial posted by Patent Owner. Petitioner also argued that the challenged claims were obvious over the clinical trial and an international patent application filed by a group of scientists employed by Patent Owner. Petitioner’s remaining grounds of unpatentability asserted that the challenged claims were obvious over the clinical trial, the patent application and an additional prior art reference.

As an initial matter, Patent Owner argued that the clinical trial, which was posted before the critical date of the challenged patent, was nevertheless not publicly available by that date and therefore not prior art. Petitioner provided testimony of an expert who had worked on drafting the statute governing ClinicalTrials.gov. The expert testified that the website was designed to be a consumer-friendly database to be used by members of the public. Petitioner’s expert also showed how the clinical trial could be found by a person of ordinary skill in the art by searching for the clinical trial number. Patent Owner faulted Petitioner’s expert for not showing how to find the clinical trial by searching keywords such as “tocilizumab” or “rheumatoid arthritis,” as a POSA might have done. Patent Owner also argued that keyword searches on ClinicalTrials.gov are not always reliable because the names of drugs and health conditions are not standardized. The PTAB disagreed that these alleged deficiencies rendered the clinical trial not publicly available before the critical date for the patent.

After finding that the clinical trial was prior art to the challenged patent, the PTAB determined that nine of the 12 challenged claims were anticipated by the clinical trial. The PTAB found that the clinical trial disclosed a method of treating rheumatoid arthritis comprising subcutaneously administering tocilizumab as a fixed dose of 162 mg per dose every week or every two weeks, as recited by two independent claims. Patent Owner argued that the clinical trial did not anticipate the challenged claims because the prior art trial did not teach administering tocilizumab in a single injection or that the method was efficacious. The Board rejected these arguments as inconsistent with the adopted claim construction, which required neither administration of tocilizumab as a single injection nor efficacy.

Turning to Petitioner’s second ground of unpatentability, the PTAB found that the same nine challenged claims were also obvious over the clinical trial combined with the international patent application filed by Patent Owner. The international patent application taught high-concentration formulations for administration of antibodies in a single subcutaneous injection. The PTAB was persuaded that a POSA would be motivated to combine the teachings of the international patent application with the tocilizumab clinical trial with a reasonable expectation of success because the patent application was published by Patent Owner, which was known for innovating tocilizumab. Thus, even if the challenged claims require a single subcutaneous injection, contrary to the Board’s claim construction, the challenged claims would still be unpatentable as obvious over the clinical trial and the international patent application.

Practice Tip: Publishing scientific findings serves a strategic benefit of creating prior art to potentially invalidate the patents of competitors. Such publication may even be required, as in the case of clinical trials. However, a prospective patent applicant should take care to avoid creating prior art against itself. It is especially important to coordinate between inventors and patent agents to ensure that a patent application is timely filed such as to avoid attacks based on any unintended public disclosure of the claimed invention.

Celltrion, Inc. v. Chugai Seiyaku Kabushiki Kaisha, No. IPR2022-00578, Paper 78 (P.T.A.B. August 29, 2023).

Share This Insight

Previous Entries

IP Newsflash

February 12, 2025

The Federal Circuit recently reversed a district court decision that found a patent that did not describe after-arising technology failed to satisfy the written description requirement. In so doing, the Federal Circuit explained that written description and enablement are evaluated based on the subject matter that is claimed, not the products that practice those claims. As a result, the patentee was not required to describe unclaimed, later-discovered features of the accused products despite the broad language in the claims that undisputedly covered the products.

...

Read More

IP Newsflash

January 24, 2025

The District of Delaware recently rejected a patentee’s argument that non-production of an opinion letter from counsel, combined with knowledge of the patent, warranted a finding that defendant induced infringement.

...

Read More

IP Newsflash

January 17, 2025

The District of Delaware recently denied a motion to dismiss a patent infringement complaint involving gene editing technology that sought relief under the Safe Harbor Provision of the Hatch-Waxman Act. Specifically, the court found the patentee’s complaint sufficiently alleged at least some uses of the claimed technology that, when taken as true, were not solely uses of a “patented invention” that were “reasonably related” to an FDA submission.

...

Read More

IP Newsflash

January 17, 2025

The District of Arizona recently held that a plaintiff’s failure to mark patented products during the time period that marking was required barred it from recovering all pre-notice damages, including for a period of time when there was no obligation to mark.

...

Read More

IP Newsflash

January 16, 2025

The Unified Patent Court (UPC) aims to provide expeditious decisions for its litigants. That means that there is a higher bar for obtaining extensions of time. As exemplified in BMW v. ITCiCo, the UPC’s reluctance to grant extensions can have serious consequences, including revocation of the patent.

...

Read More

IP Newsflash

January 15, 2025

The Patent Trial and Appeal Board granted institution of inter partes review of a patent directed to delivery of targeted television advertisements. The board rejected patent owner’s argument that a lack of particularity as to the asserted grounds justified denial under 35 U.S.C. § 312(a), holding that “simply including a significant amount of testimony and a number of supporting references is not, by itself, a reason to find that the particularity requirement is not met.”

...

Read More

IP Newsflash

December 2, 2024

The Patent Trial and Appeal Board determined that a reference could be used as prior art because patent owner failed to provide sufficient evidence that the prior art’s disclosure was invented by all four named inventors, and thus the same “inventive entity,” as the challenged claims.

...

Read More

IP Newsflash

December 2, 2024

The Patent Trial and Appeal Board rejected a patent owner’s assertion that petitioner should have named a third party, which was a defendant in a related district court patent infringement litigation and a party to a joint defense agreement (JDA) with petitioner, as a real party-in-interest (RPI). Had the board ruled otherwise and found the third party to be an RPI, the petition would have been time-barred under 35 U.S.C. § 315(b).

...

Read More

© 2025 Akin Gump Strauss Hauer & Feld LLP. All rights reserved. Attorney advertising. This document is distributed for informational use only; it does not constitute legal advice and should not be used as such. Prior results do not guarantee a similar outcome. Akin is the practicing name of Akin Gump LLP, a New York limited liability partnership authorized and regulated by the Solicitors Regulation Authority under number 267321. A list of the partners is available for inspection at Eighth Floor, Ten Bishops Square, London E1 6EG. For more information about Akin Gump LLP, Akin Gump Strauss Hauer & Feld LLP and other associated entities under which the Akin Gump network operates worldwide, please see our Legal Notices page.