Finnegan has decades of experience with ex parte reexamination (EPR) proceedings, through which the U.S. Patent and Trademark Office (USPTO) reviews patent claims against new prior art. Our patent attorneys advise clients on using EPRs to gain an edge in strengthening claims for enforcement leverage. In developing case strategy for district courts and the U.S. International Trade Commission (ITC), our litigation teams consider inter partes review (IPR) proceedings at the Patent Trial and Appeal Board (PTAB) as well as EPR requests before the Central Reexamination Unit (CRU), which can be filed anonymously. Because filing an EPR request is permissible at any time during a patent’s enforceability period, the multifunctional tool provides ongoing tactical options for both patentees and third-party challengers as part of a comprehensive IP strategy.
Ex parte reexamination is a strategic way for patentees to strengthen patents by asking the USPTO to re-review them against prior art. Successfully completing this process reinforces the presumption of validity, making the patents harder to challenge and more defensible in litigation. It also allows for claim amendments that clarify scope, reducing ambiguity and improving enforceability. A reexamined patent signals strength to competitors, deterring infringement and increasing confidence among potential licensees, which can enhance licensing value. In short, ex parte reexamination is an investment that reduces risk, supports litigation, and maximizes the commercial value of your intellectual property.
Challenging the validity of the asserted patent through new prior art creates uncertainty that weakens the accuser’s position. Courts often stay litigation during reexamination, buying time and reducing risk. If claims are canceled or narrowed, damages exposure drops, and leverage in settlement negotiations increases. Initiating reexamination shifts the balance, turning a defensive posture into a proactive competitive advantage.
EPR and IPR offer distinct strategic advantages in litigation. EPR is conducted by USPTO examiners and involves only the patent owner after the request is filed, making it useful for creating validity uncertainty and potentially delaying proceedings. IPR, on the other hand, is an adversarial process before the PTAB, with both parties actively participating in trial-like procedures. It must be filed within one year of an infringement complaint and can result in estoppel for the petitioner. IPR typically concludes within 12–18 months, while EPR often takes longer, influencing timing and leverage in disputes.
Obtained complete victory against Carrum on appeal of the District of Delaware’s claim construction to the Federal Circuit following Carrum’s stipulation of non-infringement under the claim construction, thereby exonerating BMW’s ACC system, first sold in 2000, against Carrum’s 2004 patents. Invalidated several asserted claims through post-grant efforts before the U.S. Patent Office, including IPRs and EPRs, and pursued claims through proceedings before the Eastern District of Virginia to vindicate BMW’s patent challenges.
1:18-cv-01645, D. Del., Judge Andrews
21-1435, 24-1480, Fed. Cir., Judges Clevenger, Cunningham, Lourie, Moore, Prost, Taranto
IPR2019-00902, -00903, -00904, -00905, -00927, 00928, PTAB, Judges Browne, Scanlon, Tornquist
90/019,010, CRU
Represented DuPont in Federal Circuit appeal from Board decision in inter partes reexamination proceeding relating to transgenic soybean technology, leading to affirmance of the decision in DuPont’s favor.
17-1032, -1098, Fed. Cir.
2:06-cv-00334, E.D. Tex., Judges Folsom, Gilstrap
2:07-CV-02196, C.D. Cal., Judges Klausner, Mumm, Quinn
2:07-ml-01816, C.D. Cal., Judges Klausner, Mumm
CBM2015-00053, PTAB, Judges Busch, Cocks, Wormmeester
Ex Parte Reexamination No. 90/013,586, USPTO, Judge Ralis
2:15-cv-02329, W.D. Tenn., Judges McCalla, Pham
09-1450, -1451, -1452, -1468, -1469; 10-1017, Fed. Cir., Judges Bryson, Lourie, Newman
Member of team that represented Abbott Vascular in inter partes reexaminations related to biocompatible materials for medical devices.
Reexamination Nos. 95/000,552, 95/000,542, USPTO, Judge Jones
95/001,679, 95/001,746, 95/001,792, 95/001,851, 95/001,856, USPTO, Judges Foster, Hughes, Peikari, Pokrzywa
4:11-cv-05367, N.D. Cal., Judges Hamilton, Ryu
4:14-cv-04894, N.D. Cal., Judges Beeler, Hamilton, Seeborg
IPR2014-00833, PTAB, Judges Droesch, Lee, Zecher
16-1911, Fed. Cir., Judges Dyk, Hughes, O'Malley
At the PTAB Blog
Discretion All the Way Down: USPTO Uses a Discretionary IPR Denial to Justify a
§ 325(d) EPR Denial
May 28, 2026
IP Updates
April 3, 2026
Articles
EPR Academy, Part 2 of 6: The EPR Process – From Request to Reexamination Certificate
December 5, 2025
Articles
EPR Academy, Part 1 of 6: Introduction to EPR - Understanding Ex Parte Reexamination at the USPTO
October 21, 2025
Press Release
April 28, 2026
Press Release
April 24, 2026
Award/Ranking
Finnegan Named Law Firm of the Year for Patent Law in the 2026 Best Law Firms Rankings
November 6, 2025
Press Release
April 7, 2025
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