Federal Circuit: Obviousness-type Double Patenting Does Not Apply Where Licensor Retains Secondary Right to Sue

Jul 17, 2017

Reading Time : 3 min

Background

This case arose in litigation under the Biologics Price Competition and Innovation Act (BPCIA) over Erelzi®, Sandoz’s biosimilar of Immunex’s biologic drug Enbrel® (etanercept), used for reducing the symptoms of rheumatoid arthritis. The patents at issue, U.S. Patent Nos. 8,063,182 (“’182 patent”) and 8,163,522 (“’522 patent”) are directed to the fusion protein etanercept and the methods of making it, which is the active ingredient in Enbrel®.

The applications that eventually issued as the patents-in-suit were filed by Hoffman-La Roche Inc. (“Roche”). After obtaining FDA approval for Enbrel®, Immunex entered a license agreement for Roche’s related patent applications and all patents that issued from them. Amgen later acquired Immunex, and in 2004, Amgen, Immunex and Roche entered into an “Accord and Satisfaction” agreement (the “Agreement”) to eliminate the continuing obligations to pay royalties to Roche under the initial license agreement. Under the Agreement, Immunex received a paid-up, irrevocable, exclusive license to the patents-in-suit, as well as “the sole right to grant sublicenses and to make, have made, use, sell, offer for sale, and import products covered by the patent.” Immunex also received “the exclusive right to prosecute patent applications in the U.S. patent family.” Roche, meanwhile, retained a secondary right to sue and the right to practice the invention for internal, research purposes. The agreement also prohibited either party from assigning its rights to a third party without the written consent of the other.

In 2016, Immunex, together with Roche, sued Sandoz for infringement of the ’182 and ’522 patents under the BPCIA. Sandoz stipulated to infringement, but challenged the validity of the patents on multiple grounds. Following a bench trial, the district court found, inter alia, that Sandoz failed to show that Immunex owned the patents-in-suit, and thus refused to invalidate them for obviousness-type double patenting in view of other Immunex-owned patents.

Obviousness-Type Double Patenting

On appeal, Sandoz challenged the district court’s ownership determination based on the Agreement. Sandoz argued, borrowing the “all substantial rights” test used to determine standing to sue under 35 U.S.C. § 281, that even though the patents-in-suit are assigned to Roche, the rights conveyed to Immunex through the Agreement were tantamount to an assignment of ownership. Sandoz noted that Immunex held an exclusive license to the patents-in-suit, as well as the right to sue for infringement and to control prosecution, and was, therefore, the effective patentee. And, according to Sandoz, if a party is the effective patentee for the purposes of bringing suit, it should be viewed similarly for the purposes of applying the obviousness-type double patenting doctrine.

Immunex responded that obviousness-type double patenting requires common ownership “at the time of the invention,” which did not exist here. And, in any event, obviousness-type double patenting should not apply because Roche retained some rights in the patent under the Agreement, including a secondary right to sue; the right to practice the patents for internal, non-clinical research; and the right to veto any assignment of Immunex’s interest under the agreement to another party.

Regarding the appropriate test for common ownership for the purposes of applying obviousness-type double patenting, the Federal Circuit largely sided with Sandoz. That is, the court held that the “all substantial rights” test can be informative as to whether patents are commonly owned. However, the court refused to apply the test as a strict standard for determining common ownership. Instead, it held that the “all substantial rights” test aids in preventing unjustifiable issuance of claims that are patentably indistinct from claims already owned by that party where one of the rights transferred is the right to prosecute the patents at issue. The court rejected Immunex’s assertion that ownership should be viewed at the time of the invention as inconsistent with precedent.

On the question of ownership, the court sided with Immunex, and held that the patents-in-suit were not owned by Immunex because Roche retained certain rights in the patents. In particular, Roche’s ability to exercise a secondary right to sue and the fact that neither party could assign its rights to third parties without the written consent of the other demonstrated that Roche did not transfer all substantial rights in the patents to Immunex. And for this reason, the Federal Circuit affirmed the district court’s finding that the patents-in-suit could not be invalidated for obviousness-type double patenting.

Practice Tip: This decision highlights the importance of considering specific provisions when drafting licensing agreements. In particular, when drafting a license that transfers substantial rights, including the right to prosecute patents, careful consideration should be given to the remaining rights and interests held by each party to the agreement in order to avoid later questions regarding validity.

Immunex Corp. v. Sandoz Inc., No. 2020-1037 (Fed. Cir. Jul. 1, 2020).

Share This Insight

Previous Entries

IP Newsflash

November 14, 2025

The Ninth Circuit recently reversed a district court’s decision to strike a plaintiff’s trade secret claims under the Defend Trade Secrets Act (DTSA) at the discovery stage. In doing so, the Ninth Circuit made clear that under the DTSA, whether a party defined their trade secret with sufficient particularity is a question of fact that generally does not lend itself to resolution in the absence of at least some discovery. This ruling contrasts with the California Uniform Trade Secrets Act (CUTSA), which requires a party to define their trade secrets with reasonable particularity before commencing discovery.

...

Read More

IP Newsflash

November 11, 2025

The Federal Circuit recently vacated a summary judgment ruling of invalidity, holding that the district court erred in applying preclusive effect to the Patent Trial and Appeal Board’s unpatentability findings regarding other claims in the same patent. In doing so, the Federal Circuit reiterated that issue preclusion does not apply where the prior factual determinations were made under a lower standard of proof.

...

Read More

IP Newsflash

November 3, 2025

The Federal Circuit recently clarified the requirement for work disclosed in a reference to qualify as “by another” under pre-AIA Sections 102(a) and (e), holding that there must be complete inventive identity between the information disclosed in the asserted reference and the inventors named on the relevant patent. 

...

Read More

IP Newsflash

October 31, 2025

The District Court for the Northern District of California recently granted a defendant’s motion to bifurcate, ordering that issues related to PGR estoppel should be decided in a bench trial, while the remaining issues in the case should proceed to a jury trial.

...

Read More

IP Newsflash

October 31, 2025

The Northern District of Iowa recently held that a defendant’s motion for partial summary judgment of invalidity was barred after the PTAB issued final written decisions, regardless of when the motion was filed. The defendant filed its motion before the final written decisions were issued, but the court rejected the defendant’s argument that the timing of the motion insulated it from estoppel.

...

Read More

IP Newsflash

October 1, 2025

In a recent final written decision, the PTAB determined that a reference patent was not prior art, despite the petitioner’s post‑filing attempt to correct its petition. While the petitioner argued that it intended to rely on the patent application’s earlier date of publication, both the corrected petition and the expert declaration continued to reference the issued patent rather than the published application.

...

Read More

IP Newsflash

September 30, 2025

The USPTO Director recently granted a petitioner’s request for rehearing of the decision discretionarily denying institution of inter partes review, ultimately vacating the original decision, and referring the petition to the board for an institution decision.

...

Read More

IP Newsflash

September 25, 2025

In considering claims to a method of reducing cardiovascular events, the Federal Circuit held that the term a “clinically proven effective” amount did not render the claims patentable over the prior art. Specifically, the Federal Circuit held that the “clinically proven effective” amount, whether limiting or not, could not be used to distinguish the prior art because the claims also specified the exact amount of the drugs to be administered in the method. The Federal Circuit also rejected patentee’s evidence of unexpected results because that evidence was tied solely to the “clinically proven effective” limitation.

...

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.