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Patenting Pharmaceutical Drug Formulations: Withstanding Litigation and PTAB Challenges

Recording of a 90-minute premium CLE webinar with Q&A


Conducted on Tuesday, December 10, 2019

Recorded event now available

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Program Materials

This CLE webinar will provide guidance to patent counsel on patenting drug formulations from drafting through patent prosecution and enforcement. The panel will examine lessons learned from the case law and offer strategies to overcome the potential challenges.

Description

The development of pharmaceutical products for FDA approval in the U.S. is often expensive and unpredictable. Not surprisingly, such products are often the subject of more than one patent. There is a recent trend for ANDA filers not to challenge a drug substance patent, which regularly issues from a medicinal chemistry patent application. Instead, the ANDA filers are going after the drug product patents, which can be all about formulations, particularly if the expiration date of the U.S. formulation product patent is after that of the drug substance patent.

Formulations, however, may evolve and provide different means of administration and/or dosing compared to the medicinal chemistry patent. The formulation, as it is developed over time, may be separately patentable over earlier U.S. patent filings and might offer many years of additional patent exclusivity.

Pharmaceutical formulation technology can be highly sophisticated and possess unpredictability and novelty relative to the disclosure of the medicinal chemistry U.S. patent. Challenges arise as the USPTO may insist that formulation claims in these subsequent applications be very narrow.

Paragraph IV ANDA filers may take the position that their generic formulation does not infringe such narrow claims. On the other hand, ANDA filers may also try to invalidate formulation claims. Recent Federal Circuit opinions such as Endo Pharmaceuticals Solutions Inc. v. Custopharm Inc. demonstrate how unpredictability in the art can support the patentability of drug formulation claims.

But a challenge may remain in obtaining pharmaceutical formulation claims that are broader than mere picture claims. Patent drafters may benefit from using the Section112(f) (means-plus-function) format for formulation claims. The panel will analyze Judge Salas' construction of a pharmaceutical means-plus-function claim in Nautilus Neurosciences Inc. v. Wockhardt, United States LLC (D.N.J. 2013).

To be sure, a means-plus-function claim may be construed narrowly, but the kicker is that in addition to the structure, materials, and acts in the specification, the patent owner gets equivalents thereof, and that has been construed as literal equivalents to the means. What "literal equivalents" means exactly is unclear as there is scarce judicial guidance for pharmaceutical formulations in the case law.

However, as shown in Ex parte Gleave, Appeal No. 2012-004973 (2014), drafting a formulation claim as "a composition comprising a means for [effect] and a pharmaceutically acceptable carrier," may be a successful prosecution strategy.

Biosimilars present a developing area of case law for formulation claims. The panel will discuss formulation claims in a biosimilar context.

Listen as our authoritative panel of U.S. patent attorneys teaches how to successfully prosecute and withstand litigation and PTAB challenges of formulation claims.

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Outline

  1. Overview of recent treatment of pharmaceutical formulation claims
    1. Courts
    2. PTAB
  2. Overview of recent treatment of biosimilar formulation claims
    1. Courts
    2. PTAB
  3. Section 112(f)
    1. Ex parte Gleave, Appeal No. 2012-004973 (2014)
    2. Nautilus Neurosciences Inc. v. Wockhardt, United States LLC (D.N.J. 2013)
    3. Benefits of using means-plus-function claims
    4. Challenges/limits with applying means-plus-function claims
  4. Litigation considerations for formulation claims

Benefits

The panel will review these and other important issues:

  • What steps can counsel for patentees take during drafting to avoid written description and enablement problems and withstand invalidity/unpatentability challenges based on written description and enablement?
  • What steps should patent counsel take to balance showing unpredictability for nonobviousness with showing fulfillment of the enablement and written description requirements?
  • How to use means-plus-function claims for pharmaceutical formulations against ANDA filers and/or 505(b)(2) filers
  • What factors does counsel need to keep in mind when litigating formulation claims?

Faculty

Cyr, Shana
Shana K. Cyr, Ph.D.

Partner
Finnegan Henderson Farabow Garrett & Dunner

Dr. Cyr represents clients in complex patent litigations, contentious proceedings before the USPTO, and appeals related...  |  Read More

Hasford, Justin
Justin J. Hasford

Partner
Finnegan Henderson Farabow Garrett & Dunner

Mr. Hasford has experience in all areas of intellectual property law. His practice focuses on complex patent litigation...  |  Read More

Irving, Thomas
Thomas L. Irving

Partner
Finnegan Henderson Farabow Garrett & Dunner

Mr. Irving has 35 years of experience in the field of IP law. His practice includes due diligence, patent prosecution,...  |  Read More

Rudolph, Barbara
Barbara R. Rudolph, Ph.D.

Partner
Finnegan Henderson Farabow Garrett & Dunner

Dr. Rudolph has successfully litigated complex Hatch-Waxman Paragraph IV Abbreviated New Drug Application and...  |  Read More

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