[Webinar] Obviousness-Type Double Patenting and USPTO Proposed Rules for Terminal Disclaimers - Recent Court Treatment, Implications for Patent Strategy and Enforceability

July 2nd, 1:00 pm - 2:30 pm EDT
Strafford
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July 2nd, 2024
1:00 PM - 2:30 PM EDT
$ 278.00

A live 90-minute premium CLE video webinar with interactive Q&A


This CLE webinar will guide patent counsel on obviousness-type double patenting (ODP), including the recent decisions that have relied on Cellect. The panel will also discuss the USPTO's proposed terminal disclaimer rule and will offer best practices for addressing ODP and terminal disclaimers.

Description

Recently, two courts relied on the decision in In re Cellect, but landed on opposite sides of the fence. The appeal of one of those decisions, by Judge Andrews in Allergan U.S. Inc. v. MSN Labs. Pvt. Ltd., was recently argued, and it appears the decision on ODP may be heading for reversal.

Also affecting double patenting, the United States Patent and Trademark Office (USPTO) published on May 10, 2024, its proposed rule that would change current terminal disclaimer practices and could significantly impact prosecution strategy as well as the enforceability of these patents.

Under the proposed rule, terminal disclaimers will need to include an agreement that the patent would be unenforceable if the patent claim to which it is tied is found to be invalid or unpatentable and appeals have been exhausted. Amongst the bar representing patentee, this proposal is very unpopular.

Listen as our authoritative panel of patent attorneys examines ODP, including the recent decisions that have relied on Cellect. The panel will also discuss the USPTO's proposed terminal disclaimer rule and will offer best practices, such as safe harbor/election/restriction and two-way test for ODP, for addressing ODP and terminal disclaimers.

Outline

  1. Allergan argument and recent court treatment
  2. Implications of the recent decisions on ODP practice
  3. USPTO proposed rule
  4. Best practices

Benefits

The panel will review these and other key issues:

  • How do recent decisions impact the scope of ODP?
  • What are the steps to defeat double patenting rejections?
  • What are the steps to avoid ODP rejections?
  • What potential impact will the USPTO proposed terminal disclaimers rule have?

FACULTY

Irving, Thomas

Thomas L. Irving
Partner
The Marbury Law Group

Mr. Irving has 47 years of experience in the field of IP law. His practice includes due diligence, patent prosecution, reissue and reexamination, patent interferences, and counseling, including prelitigation, Orange Book listings of patents covering FDA-approved drugs, and infringement and validity analysis in the chemical fields, as well as litigation. He has served as lead counsel in many patent interferences.

Murphy, Amanda

Dr. Amanda K. Murphy, Ph.D.
Partner
Finnegan Henderson Farabow Garrett & Dunner

Dr. Murphy focuses her practice on client counseling and patent prosecution for a range of clients. She prepares new patent applications, prosecutes U.S. and foreign applications, and represents applicants at appeals and oral hearings before the PTAB. She has experience in prosecuting inter partes and ex partes reexamination applications, reissue applications, and patent term extension applications for approved pharmaceuticals, including obtaining supplemental protection certificates in Europe.

O’Brien, Michelle

Michelle E. O'Brien
Partner
The Marbury Law Group

Ms. O’Brien has more than 20 years of experience representing domestic and foreign clients of all sizes in patent procurement, litigation, and client counseling, with a particular emphasis on chemical, biochemical, and pharmaceutical technologies. Exemplary areas of her technical expertise include polymer chemistry; ceramics; glass; food chemistry; cosmetics; paper products; adhesives; and pharmaceutical products, including new chemical entities and formulations and novel solid forms, including polymorphs, cocrystals, and amorphous forms of compounds.

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