Under Director Squires’ leadership, the PTAB has seen reduced reliance on discretionary denials and a recalibrated role for inter partes review. This session brings together former PTAB faculty and experienced PTAB litigators to examine how institution standards are being applied in practice, why certain challenges are proving less viable than before, and when alternatives such as ex parte re-examination may offer a more effective path.
- Why challengers are re-assessing IPR risk and turning to ex parte re-examination, including trade-offs around timing, estoppel, and examiner workload.
- How patent owners are using PTAB uncertainty to influence parallel litigation and settlement leverage.
- Practical guidance on selecting and sequencing invalidity tools in the current PTAB environment
- Consider venues in alternative jurisdictions such as the EPO and UPC.

Deborah Sterling

Ryan Daniel

Victoria Reines

Scott E. Kamholz
This judges’ panel offers candid insight into how courts approach patent disputes involving complex technologies, including software, electronics, and standards-based products. Drawing on recent decisions and, judges from key US jurisdictions will discuss what most influences outcomes from claim construction and technical tutorials to expert testimony and damages models.

Klaus Grabinski

Christopher J. Burke

MaryJoan McNamara

Roy S. Payne

Mark Baghdassarian
Hatch-Waxman case outcomes are often decided by early choices that shape risk, cost, and leverage long before trial. This session offers a structured review of how companies are building and defending Hatch-Waxman cases, from the first Paragraph IV notice through to final judgement.
- Identify strategic decision points from Paragraph IV notice to trial, and where early decisions most influence outcomes.
- Review recent key Hatch-Waxman cases and examine how their outcomes have influenced litigation strategy.
- Managing evidence, discovery scope, and expert strategy.
- Compare US Hatch-Waxman litigation strategy to parallel approaches in Canada and other key jurisdictions, including differences in timing, remedies and leverage.

Kevin Yurkerwich

Laura Chubb

Megan Chacon

John Kirkland
First enacted in 1979, and the basis of all modern US Trade Secret legal regulations, including the establishment of the DTSA, in August 2026 the Uniform Law Commission’s Drafting Committee’s will meet to discuss potential updates to the Uniform Trade Secrets Act (UTSA). Originally drafted to resolve inconsistencies in the treatment of trade secrets across state lines, there has since been debate as to whether the act still meets its original intentions. Proposed reforms aim to address this through key aspects of the statute, including reasonable measures, extraterritorial reach, damages, and the interaction between the UTSA and DTSA. This session will review recent changes to the UTSA, discuss ensuing strategy, and consider the effect on the DTSA, and how it may be adapted in response.
- How UTSA jurisprudence has evolved since its last amendment in 1985, including divergent state court approaches to reasonable measures, trade secret identification, and the "reasonable under the circumstances" standard.
- Concerns around inconsistencies in state-by-state adoption of the UTSA and whether it still achieves the uniformity it was designed to deliver.
- How courts are addressing the UTSA's limited extraterritorial reach, and the growing trend toward hybrid state-federal (UTSA-DTSA) filings to extend jurisdictional coverage.
- Review the Uniform Law Commission's Drafting Committee's proposed updates to the UTSA and consider how any resulting changes may require corresponding adaptation of the DTSA.

Ken Corsello
Ken Corsello is an IP Law Counsel at IBM. He currently focuses on drafting and negotiating patent licenses and assignment agreements. At IBM, he has worked on patent procurement, litigation, client counseling, product clearance, and IP transactional matters.
Before joining IBM, Ken was a law clerk to Chief Judge Glenn Archer at the Federal Circuit; an Associate Solicitor in the USPTO; and in private practice at law firms in Washington, D.C. He did his undergraduate work in Computer Science at SUNY Stony Brook, received his JD from the Catholic University, and obtained an LL.M. from George Washington University.
Ken has been the chair of IPO’s Trade Secrets Committee since 2016. His recent presentations on trade secret law include participating in a panel at the USPTO’s “Trending Issues in Trade Secrets: 2019” symposium and as a witness on behalf of IPO at the 2018 hearing on “Safeguarding Trade Secrets in the United States” held by the U.S. House Committee on the Judiciary, Subcommittee on Courts, Intellectual Property, and the Internet.
This presentation uses litigation and settlement data to examine how patent type, timing, and strategy influence settlement outcomes, retained exclusivity, and overall leverage across pharma patent litigation.

Charles Haisch

Scott Allen
Join this session for a review of recent trade secret cases and outcomes across key jurisdictions in the US and further afield; examine how reasonable measure standards have evolved, and what courts are now accepting.

William Logan
Gain firsthand insight into how judges from the PTAB and federal courts in key jurisdictions are approaching pharmaceutical and biotech patent disputes. This session offers a rare opportunity to hear directly from the decision-makers on litigation strategy, evidentiary expectations, and what most influences outcomes in complex patent cases.

Klaus Grabinski

Roy Payne

Kent Jordan
Kent A. Jordan is a Director in the Wilmington, Delaware law firm of Richards, Layton & Finger. Previously, since 2006, he served as a United States Circuit Judge for the Third Circuit. Before that, he was a United States District Judge for the District of Delaware from 2002 to 2006. Judge Jordan received a B.A. in Economics in 1981 from Brigham Young University and a J.D. in 1984 from Georgetown University. He was an Assistant United States Attorney and head of the Civil Division in the U.S. Attorney’s Office for the District of Delaware. Later, he served as an officer and as a member of the boards of directors of privately held businesses and was a partner in a law firm. He is an Adjunct Professor of Law at the University of Pennsylvania and Vanderbilt University and has served as President of the Board of Trustees of the American Inns of Court Foundation, as well as on the boards of other non-profit organizations.

Christopher J. Burke

Brian P. Murray
Brian counsels clients across the biotechnology, pharmaceutical, chemical, and engineering industries on complex intellectual property and technology disputes. He represents companies in high-stakes patent litigation involving biotechnology and biosynthesis, pharmaceuticals, plastics, telecommunications, and LED technologies, helping clients align legal strategies with scientific, regulatory, and business objectives.
Drawing on his background in pharmaceutical research and development, Brian represents clients in Hatch-Waxman litigation and has helped guide multiple matters through trial. He also advises those pharmaceutical clients on pre-suit strategy, product selection, portfolio management, formulation development, labeling considerations, and regulatory matters.
A significant portion of Brian’s practice focuses on biotechnology innovators, particularly those developing bioengineering and fermentation technologies. He has extensive experience litigating patents related to metabolic engineering and microbial strain development and is skilled at translating highly technical concepts into clear, compelling litigation and counseling strategies.
Before attending law school, Brian worked as a formulation development scientist at Caraco Pharmaceutical Laboratories and gained experience in pharmaceutical synthesis at Fabbrica Italiana Sintetici S.p.A., providing him with a practical understanding of the industries he serves.
In light of recent changes in PTAB practice under new USPTO Director John A. Squires, in-house teams are reassessing disclosure risk, IPR exposure, and long-term enforceability, particularly for manufacturing processes, algorithms, and data-driven know-how. This session focuses on how companies are making these calls in practice, and how patent strategy is directly shaping trade secret risk in later disputes.
- How PTAB institution trends, discretionary denial, and parallel-proceeding strategy are influencing decisions to rely more heavily on trade secrets.
- Where patent specifications, prosecution history, and expert positions have later been used to argue that information was disclosed and no longer secret.
- Managing the risk of over-disclosure in patent filings while preserving meaningful trade secret protection.
- When companies deliberately shift from patenting to trade secret protection over a product’s lifecycle, and what triggers that shift.

Erica LoRe

Damon Gupta
Damon Gupta is a Director, Patent Counsel at Spark Therapeutics, Inc., a leader in gene therapy and member of the Roche Group. With over a decade of experience in intellectual property (IP) law and a background in molecular biology, Damon advises biotechnology and pharmaceutical companies on patent strategy, IP transactions, and risk mitigation. At Spark, Damon leads efforts to protect proprietary assets, including trade secrets, manage IP disputes, and provides IP support to cross-functional teams, including R&D, manufacturing, and corporate transactions. Damon holds a J.D. from Chicago-Kent College of Law, an M.S. from Baylor College of Medicine, and a B.S. from The Ohio State University.

Julie Lappin
Julie is a Senior IP Counsel at Nestlé S.A. She has worked for multiple business units in her 14+ year career with Nestlé, including Coffee, Nestlé Health Science, and PetCare. Julie significantly contributed to developing and deploying Nestlé's trade secret protection program. Before joining Nestle, she was a Corporate Patent Counsel at Pfizer Inc.
