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Qualcomm v. Apple — Federal Circuit Holds Applicant-Admitted Prior Art Cannot Serve as Basis for IPR Petition

The Federal Circuit held that statements in a patent’s own specification acknowledging known prior art — so-called applicant-admitted prior art (AAPA) — cannot serve as the “basis” for an inter partes review petition under § 311(b), which limits IPR to prior art consisting of patents and printed pub

Federal Circuit
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Masimo Corp. v. True Wearables, Inc. — Federal Circuit Upholds Trade Secret Injunction, Holds Prior Publication in Unrelated Field Does Not Destroy Secrecy

The Federal Circuit affirmed a preliminary injunction protecting Masimo’s pulse oximeter algorithm as a trade secret, holding that prior publication of equivalent mathematics in a statistics journal did not make the algorithm generally known to those who could obtain economic value from it in

Federal Circuit
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Teva Pharmaceuticals USA v. Corcept Therapeutics — Federal Circuit Requires Petitioner to Show Reasonable Expectation of Success for Specific Claimed Dosage

The Federal Circuit affirmed PTAB’s refusal to invalidate Corcept’s mifepristone dosage patent, holding that an IPR petitioner must demonstrate a reasonable expectation of success for the specific dosage claimed — not merely for the drug combination generally.

Federal Circuit
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Biogen v. Mylan — Federal Circuit Affirms Invalidity for Lack of Written Description Where Single Dosage Mention Was Insufficient

In a divided decision, the Federal Circuit affirmed that Biogen’s multiple sclerosis drug patent lacked adequate written description because the specification’s single passing reference to a 480 mg/day dose of dimethyl fumarate did not demonstrate the inventors actually possessed that specific thera

Federal Circuit
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Celgene Corp. v. Mylan Pharmaceuticals — Federal Circuit Clarifies Hatch-Waxman Venue: It’s Where the ANDA Was Submitted, Not Where Drugs Will Be Sold

The Federal Circuit affirmed dismissal of Celgene’s Hatch-Waxman patent suit for improper venue, holding that for ANDA litigation venue purposes, the act of infringement is the submission of the ANDA itself — not the receipt of a notice letter or the state where future generic sales are antici

Federal Circuit
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University of Strathclyde v. Clear-Vu Lighting LLC — Federal Circuit Reverses IPR Obviousness Finding for Lack of Reasonable Expectation of Success

The Federal Circuit reversed a PTAB obviousness determination, holding that the Board lacked substantial evidence for a reasonable expectation of success because the cited prior art references did not actually achieve the claimed result of inactivating antibiotic-resistant bacteria without photosens

Federal Circuit
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Kannuu Pty Ltd. v. Samsung Electronics Co. — Federal Circuit Holds NDA Forum Selection Clause Does Not Bar IPR Proceedings

The Federal Circuit held that a forum selection clause in a non-disclosure agreement requiring disputes to be litigated in New York courts does not preclude the counterparty from filing inter partes review petitions at the PTAB, because the connection between the IPR and the NDA was too attenuated.

Federal Circuit
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CosmoKey Solutions GmbH v. Duo Security LLC — Federal Circuit Upholds Mobile Authentication Patent as Patent Eligible Under Alice Step Two

The Federal Circuit reversed a district court’s patent ineligibility ruling, holding that claims directed to a specific two-channel mobile authentication method that improves cybersecurity represent a concrete technical solution eligible for patent protection.

Federal Circuit
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In re Vivint, Inc. — Federal Circuit Holds USPTO May Reject Ex Parte Reexamination Requests That Recycle Failed IPR Arguments

The Federal Circuit held that the USPTO acted arbitrarily by ordering ex parte reexamination based on arguments substantially identical to those the same requester had already raised and lost in IPR proceedings, affirming the agency’s discretion to reject repetitive patent challenges.

Federal Circuit
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Belcher Pharmaceuticals, LLC v. Hospira, Inc. — Federal Circuit Affirms Patent Unenforceability for Inequitable Conduct Tied to FDA-PTO Information Disconnect

The Federal Circuit affirmed that a patent is unenforceable for inequitable conduct when a company’s chief science officer withheld from the USPTO material information about a competitor’s epinephrine product that he disclosed to the FDA during the same period.

Federal Circuit
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Lubby Holdings LLC v. Chung — Federal Circuit Holds Corporate Officers Are Personally Liable for Patent Infringement Without Piercing the Corporate Veil

The Federal Circuit held that a corporate officer can be personally liable for actively participating in a corporation’s patent infringement even without any piercing of the corporate veil, and clarified that the patent marking statute limits pre-notice damages regardless of whether the infrin

Federal Circuit
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Juno Therapeutics v. Kite Pharma — Federal Circuit Wipes Out $1.2 Billion Verdict, Holds CAR-T Genus Claims Lack Written Description

The Federal Circuit reversed a $1.2 billion jury verdict for Juno, holding that patent claims covering a broad functional genus of CAR-T cell receptor constructs lacked adequate written description because the specification disclosed only a few examples that could not support the full claimed scope.

Federal Circuit
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Universal Secure Registry LLC v. Apple Inc. — Federal Circuit Holds Multi-Factor Authentication Coordination Patents Are Abstract Ideas Ineligible Under § 101

The Federal Circuit held that four patents covering methods for coordinating multi-factor authentication across secure registries, PINs, biometrics, and universal devices are directed to abstract ideas and lack an inventive concept sufficient to confer patent eligibility.

Federal Circuit
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MLC Intellectual Property, LLC v. Micron Technology, Inc. — Federal Circuit Affirms Exclusion of Damages Expert for Insufficient Apportionment Analysis in Flash Memory Patent Case

The Federal Circuit affirmed the exclusion of a patent owner’s damages expert, holding that the expert’s reasonable royalty calculation failed to adequately apportion the royalty base to account only for the patented features, rather than the full value of the accused products.

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