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Chad A. Landmon

Partner

Chad Landmon practices primarily in the areas of patent and other intellectual property litigation and counseling and food and drug law. He chairs the firm's FDA Practice Group.

Mr. Landmon litigates intellectual property cases in federal and state courts across the country, as well as in arbitration proceedings, involving numerous industries, including pharmaceuticals, printing and packaging, power tools, and many others. Representative examples of recent patent infringement cases handled include: Roche Palo Alto LLC v. Endo Pharmaceuticals Inc., No. 10-00261 (D. Del.); Genzyme Corporation v. Endo Pharmaceuticals Inc., No. 09-02589 (D. Md.); sanofi-aventis v. Actavis South Atlantic LLC, No. 07-572 (D. Del.); Purdue Pharma L.P. v. Actavis Totowa LLC, No. 07-3972 (S.D.N.Y.); Shire LLC v. Actavis, Inc., No. 07-00718 (D. Md.); Adams Respiratory Therapeutics, Inc. v. URL/Mutual Pharmaceutical Cos., No. 06-4418 (E.D. Pa.); Cushion Technologies, LLC v. Fila USA, Inc., No. 06-347 (E.D. Tx.); Eisai Co., Ltd. v. URL/Mutual Pharmaceutical Cos., No. 06-03613-HAA-MF (D.N.J.); Whelen Engineering Co., Inc. v. Star Headlight & Lantern Co., Inc., No. 06-0299 (JCH) (D.Conn.); Arthur Blank & Co. v. Moore North America, Inc., No. 02-2282 (W.D. Tenn.); Rexon Industrial Corp. v. Ryobi Technologies, 02-1264 (D. Conn.).

A significant portion of Mr. Landmon’s practice is spent in the firm’s FDA and BioMedical Practice Groups, in which he provides counseling and litigation services relating to patent, FDA and antitrust issues involving the development and marketing of new and generic drug products and the regulation of tobacco products. The FDA matters involve numerous issues relating to the Hatch-Waxman Amendments, including marketing exclusivities, patent listing, certification and notification requirements, bioequivalence, labeling and other issues relating to the FDA approval process. Mr. Landmon has petitioned FDA and litigated disputes involving a variety of issues, including new chemical entity exclusivity, the generic exclusivity period and pediatric exclusivity. Representative examples of recent litigation involving FDA issues includes: Actavis Elizabeth LLC v. FDA, No. 09-362 (D.D.C.); Mylan Laboratories, Inc. v. FDA, No. 07-579 (D. D.C.) (representing third-party intervenor); Ranbaxy Labs, Ltd. v. FDA, No. 04-0869 (D.D.C.) (representing third-party intervenor); Purepac Pharmaceutical Co. v. FDA, No. 03-2282 (D.D.C.). Mr. Landmon has also handled Lanham Act cases relating to false advertising allegations, including in a case in which the firm obtained the dismissal of such claims based upon an argument that the claims were preempted by FDA law. See Wyeth v. Sun Pharmaceutical Indus. Ltd., 2010 U.S. Dist. LEXIS 18180, Dkt. No. 09-11726 (E.D. Mich. March 2, 2010). Mr. Landmon frequently speaks and writes about issues relating to FDA law and pharmaceutical patent litigation. He also serves on the Editorial Advisory Board of Generic Line, a publication of FDAnews.

Mr. Landmon has an active intellectual property counseling practice, in which he evaluates patent, trademark and trade secret claims. He is often involved with the product development process, assisting clients in navigating around the intellectual property rights of competitors and in designing their own patent strategies. In the course of this practice, Mr. Landmon provides advice and services to clients regarding the acquisition, management and enforcement of intellectual property portfolios. He also prepares freedom-to-operate opinions and opinions relating to the infringement and validity of patents.

Mr. Landmon also participates in matters involving the intersection of the antitrust and patent laws, including issues arising from the settlement of patent and Hatch-Waxman exclusivity disputes, the licensing of critical technology and the formulation of joint development relationships. In addition to providing advice regarding such issues, Mr. Landmon has also represented clients during FTC investigations involving such agreements.

Mr. Landmon has also been involved with commercial litigation and arbitration involving a variety of complex contract and tort law issues.

Bar & Court Admissions

  • Connecticut
  • District of Columbia
  • U.S. Court of Appeals for the District of Columbia Circuit
  • U.S. Court of Appeals for the Federal Circuit
  • U.S. Court of Appeals for the Sixth Circuit
  • U.S. District Court District of Columbia
  • U.S. District Court District of Connecticut
  • U.S. District Court Southern District of New York

Education

  • University of Connecticut School of Law, Hartford, Connecticut, 1999 J.D. with Honors. Notes & Comments Editor, Connecticut Law Review.
  • University of Connecticut, Storrs, Connecticut, 1996 B.A. Political Science with honors, and Economics, summa cum laude.

Publications

Seminars & Classes

  • ACI's FDA Boot Camp: Bioequivalence - What Patent Lawyers Need to Know (March 25, 2010, September 16, 2009, March 31, 2009, September 22, 2008, and April 1, 2008).
  • ACI's Paragraph IV on Trial: Litigator's Master Class on Paragraph IV Pre-Trial Preparation (November 11, 2009).
  • CBI's Pharmaceutical Congress on Paragraph IV Disputes and Settlements: Workshop Leader on Assessing Paragraph IV Litigation Strategies (October 23, 2009).
  • FDAnews Webinar: Assessing the Patent and FDA Strategies for Follow-On Biologics to Maximize Success (May 27, 2009).
  • ACI's Paragraph IV Disputes: Advanced Master Class - Obtaining Optimal Terms and Mitigating Antitrust Concerns When Settling Paragraph IV Disputes; Moderator of Panel on Mastering the Interplay between 180-Day Exclusivity, Forfeiture Provisions, Citizens Petitions and Paragraph IV Litigation (April 27-29, 2009).
  • CBI's Annual Summit on Biosimilars and Follow-On Biologics: Panelist on First Follow-On Biologic Exclusivity; Moderator of Panel on How Different Lengths of Exclusivity Would Affect Innovation (March 10-11, 2009).
  • ACI's Paragraph IV on Trial: Litigator's Master Class on Paragraph IV Pre-Trial Preparation (November 18, 2008).
  • CBI's Pharmaceutical Congress on Paragraph IV Disputes: Workshop Leader on Assessing Litigation Strategies to Proactively Plan for Paragraph IV Disputes; Moderator of Panel on Interpreting Forfeiture Provisions (October 15-16, 2008).
  • FDAnews Audioconference: Navigating the FDA's New 180-Day Generic Marketing Exclusivity Rulings (March 28, 2008).
  • Guest Lecturer at the University of Connecticut School of Law regarding patent law and the pharmaceutical industry, including related antitrust issues.
  • Collaborating Attorney to the Connecticut Intellectual Property Notes, an e-publication of the University of Connecticut School of Law.

Professional Activities

  • American Bar Association, Intellectual Property, Litigation and Antitrust Sections
  • American Intellectual Property Law Association
  • Connecticut Bar Association
  • Connecticut Intellectual Property Law Association
  • Hartford County Bar Association