
Sarah A. Geers
Articles
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2 weeks ago |
jdsupra.com | Jennifer Chheda Ph.D |Sarah A. Geers |Matthew Johnson
On March 26, 2025, the U.S. Patent and Trademark Office ("USPTO") acting director sent a memorandum regarding a new interim process for workload management to all Patent Trial and Appeal Board ("PTAB") judges.
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Aug 2, 2024 |
jdsupra.com | Sarah A. Geers
[co-author: Scott Findley]*On July 9, 2024, Director Vidal reversed and remanded a denial of institution of inter partes review (IPR) relating to three Spin Master patents. See Prime Time Toys LLC v. Spin Master, Inc., IPR Nos. 2023-01339, 2023-01348, 2023-01461, Paper 12 (PTAB July 9, 2024). Director Vidal found that the PTAB erred in its motivation-to-combine analysis and effectively required an expectation of “absolute success” for prior art combinations. Paper 12 at 7, 9.
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Aug 2, 2024 |
mondaq.com | Sarah A. Geers
On July 9, 2024, Director Vidal reversed and remanded a denial of institution of inter partes review (IPR) relating to three Spin Master patents. See Prime Time Toys LLC v. Spin Master, Inc., IPR Nos. 2023-01339, 2023-01348, 2023-01461, Paper 12 (PTAB July 9, 2024). Director Vidal found that the PTAB erred in its motivation-to-combine analysis and effectively required an expectation of "absolute success" for prior art combinations. Paper 12 at 7, 9.
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Jul 31, 2024 |
mondaq.com | Jennifer J. Chheda |Sarah A. Geers |Matthew Hertko |Daniel Sloan
In Short The Situation: Senate Bill 150 ("S.B. 150")—the Affordable Prescriptions for Patients Act of 2023—unanimously passed the Senate and would amend 35 U.S.C. § 272(e) to limit, under certain circumstances, the number of patents that a sponsor of an originator biological product, or RPS, may assert in an infringement action against a biosimilar applicant. The Result: S.B. 150 has been sent to the United States House of Representatives.
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Jul 9, 2024 |
jdsupra.com | Sarah A. Geers |Matthew Hertko |Anthony Insogna
In ShortThe Situation: The Hatch-Waxman Act allows generic drug manufacturers to "carve out" a brand's patented indications from their proposed labeling. Generic manufacturers often rely on these so-called "skinny labels" to try to avoid findings of infringement in standard Hatch-Waxman cases, but in post-marketing situations, the generic's "skinny label," coupled with its public statements, can be evidence of induced infringement even as to the carved-out, patented uses.
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