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

November 5, 2024

The Federal Circuit vacated a district court’s fee award because the district court considered certain information that was not relevant to the question of whether plaintiff’s case was exceptional. Specifically, the Federal Circuit held that only those “red flags” that related to the successful Section 101 defense, which served as the basis for the district court’s grant of summary judgment, could be used to show the case was fatally flawed.   

...

Read More

IP Newsflash

November 1, 2024

The Federal Circuit’s decision in Kyocera Senco Industrial Tools Inc. v. International Trade Commission articulated a bright-line test for patent expert admissibility: to testify from the perspective of a “person of ordinary skill in the art” (POSITA), the expert must at least meet the definition of a POSITA for the patents-in-suit. Absent that level of skill, Kyocera holds that the witness’s testimony is not sufficiently reliable or relevant enough to be relied on by a fact-finder.

...

Read More

IP Newsflash

October 29, 2024

The PTAB denied a petitioner’s motion to compel routine discovery that sought information from a parallel ITC investigation for alleged inconsistent positions taken by patent owner in the IPR. The board found that patent owner had not taken inconsistent positions but warned patent owner that it had an ongoing duty to produce any information inconsistent with arguments made during the present IPR, even if that information related to arguments patent owner had dropped at the ITC.

...

Read More

IP Newsflash

October 11, 2024

The Central District of California ruled that the heightened pleading standard of Federal Rule of Civil Procedure 9(b) applies to all three prongs of a false patent marking claim, including the third prong, competitive injury. In doing so, took a clear stand on an issue with a nationwide split among district courts.

...

Read More

IP Newsflash

October 10, 2024

In a patent case containing a variety of federal and state law claims, the District of Massachusetts retained supplemental jurisdiction over the state law claims even after all the federal law claims were dismissed.

...

Read More

IP Newsflash

October 3, 2024

The Federal Circuit recently upheld the USPTO’s authority under the estoppel provision 37 C.F.R. § 42.73(d)(3)(i) to prohibit a patent owner from obtaining patent claims that are not patentably distinct from claims previously declared unpatentable in inter partes review (IPR) proceedings. However, the court clarified that the regulation applies only to new claims or amended claims, not previously issued claims.

...

Read More

IP Newsflash

September 27, 2024

In Kyocera Senco Industrial Tools Inc. v. International Trade Commission, the Federal Circuit held that an expert must meet the definition of a “person of ordinary skill in the art” of the asserted patents in order to opine on infringement, among other issues. This new bright-line test and the underlying rationale, however, raised several new questions regarding expert admissibility. SeeFederal Circuit: Narrow Definition of Skill in the Art Dooms Expert’s Testimony” and “Grappling With A Bright-Line Patent Expert Admissibility Test.” The Federal Circuit recently addressed one of those questions, namely whether an expert must have acquired the requisite level of skill as of the time of the invention or whether it is sufficient for an expert to acquire that knowledge at a later date.

...

Read More

IP Newsflash

September 23, 2024

The Director of the USPTO initiated sua sponte review of a PTAB panel’s decision to impose sanctions based on patentee’s conduct during IPR proceedings. The PTAB cancelled all of patentee’s claims, including those not unpatentable on the merits, after finding that patentee deliberately withheld data relevant to the patentability of the claims at issue. In her review, the Director addressed which regulations are implicated upon a party’s misconduct during AIA proceedings and addressed whether entry of judgment in the trial was an appropriate sanction.

...

Read More

© 2024 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.