TEL2 DC - 202.721.5415
FAX CT - 860.275.8101
FAX2 DC - 202.912.4701
cal@avhlaw.com, Washington, DC
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Chad Landmon practices primarily in the areas of patent and other intellectual property litigation and counseling and food and drug law. Mr. Landmon is co-chair of Axinn, Veltrop & Harkrider LLP's intellectual property practice and chair of 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 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 Eastern District of Michigan
- U.S. District Court Southern District of New York
Articles & Newsletters
- 2012 Court Decisions Impact the Life Science Industry, January 3, 2013
- The Rise of Precompetitive Collaboration, Life Science Leader, December 5, 2012
- Generic Drug Litigation: A Growing Practice Niche, Connecticut Law Tribune, November 19, 2012
- Axinn Partner Chad A. Landmon Interviewed for Law360's Q&A, Law360, July 12, 2012
- Innovative Procedures v. Premarketing Approval, HealthLaw 360 and IPLaw360, September 20, 2011
- Final Word: Advocating for Biosimilar Approval Standards under BPCI, BioPharm International, Vol. 24, No. 9, September 2011
- Viewpoint: Advocating for Biosimilar Approval Standards under BPCI, Pharmaceutical Technology, Vol 35, Issue 6, June 2011
- The Challenges of FDA's Nascent Biosimilars Regime, Law360, November 17, 2010
- Human Tissue and Stem Cell Therapies: Revolutionary New Therapies that Face Increasing FDA Scrutiny, FDLI's Update Magazine 2010, Issue 5
- Ask the Experts: Experts Discuss Effect of NJ Rules on Hatch-Waxman Litigation, Generic Line, February 4, 2009
- Ask the Expert: Impact of Federal DJ Jurisdiction Decision, Generic Line, September 3, 2008
- Federal Circuit Draws the Line on DJ Jurisdiction, IP Law360 and Health Law360, August 25, 2008
- FDA's Exclusivity Forfeiture Saga Continues, IP Law360 and Health Law360, May 15, 2008
- Ask the Expert: Caraco's Impact on Declaratory Judgment Actions, Generic Line, May 14, 2008
- Ask the Expert: Impact of FDA's Exclusivity Forfeiture Rulings, Generic Line, April 30, 2008
- Here Comes The Tidal Wave of Generic DJ Actions, IP Law360 and Health Law360, April 3, 2008
- FDA Removes Teeth From Exclusivity Forfeiture, IP Law360 and Health Law360, January 25, 2008
- Supreme Court Backhands Key Federal Circuit Test, IP Law360, January 10, 2007
- Fourth Circuit Rejects Another Authorized Generics Challenge, IP Law360 and Health Law360, July 19, 2006
- On Demand: Focusing The Patent Scope, The Connecticut Law Tribune, Intellectual Property Supplement, May 8, 2006; also published in The Connecticut Tech Tribune, July 2006
- FDA's "Holding On The Merits" Test, IP Law360, April 21, 2006
- Recent Court Rulings Indicate That Patent Rights May Trump the Antitrust Laws, Intellectual Property Today, April 2006
- The "Narrowed Claim Conundrum" Resulting from Reissue and Reexamination Proceedings, Intellectual Property Today, Vol. 12, No. 10, October 2005
- The Impact of a Brand Generic Launch on the Recovery of Patent Damages, IPL Newsletter, Vol. 23, No. 4, Summer 2005
- Note, Creation of a Less Perfect Union: The Implications of General Motors Corp. v. Tracy for Commerce Clause Analysis of State Taxation, 30 Conn. L. Rev. 1121 (1998)
Speaking Engagements & Seminars
- American Conference Institute's Biosimilars Conference
- American Conference Institute's 7th Annual Paragraph IV Disputes Conference
- 2013 FDLI Annual Conference
- Bioequivalence--What Patent Lawyers Need to Know
- CBI's 4th Life Sciences Congress on Paragraph IV Disputes
- Partner Chad Landmon featured on Post-Marketing IP Protection and Enforcement Panel at FDLI’s “Intellectual Property Throughout the Drug Development Lifecycle: Opportunities and Challenges” conference on July 17, 2012
- ACI's FDA Boot Camp: Bioequivalence - What Patent Lawyers Need to Know
- CBI's 4th Annual Bio/Pharmaceutical Drug Safety Forum
- ACI's FDA Boot Camp Post-Conference Workshop: Non-Patent Marketing Exclusivities: Challenges, Opportunities and Current Controversies
- "Patent Due Diligence - A Good Business Practice"
- Chad Landmon Speaks on "How to Align the FDA Approval Process with Paragraph IV Strategy"
- AIPLA Mid-Winter Institute, meeting of the Special Committee on the FDA: Discussion of the FDA Hearings on the Biologics Price Competition and Innovation Act
- Chad Landmon Presented on Bioequivalence in Boston
- ACI's Paragraph IV on Trial: Litigator's Master Class on Paragraph IV Pre-Trial Preparation
- CBI's Pharmaceutical Congress on Paragraph IV Disputes and Settlements: Workshop Leader on Assessing Paragraph IV Litigation Strategies
- FDAnews Webinar: Assessing the Patent and FDA Strategies for Follow-On Biologics to Maximize Success
- ACI's Paragraph IV Disputes: Advanced Master Class - Obtaining Optimal Terms and Mitigating Antitrust Concerns When Settling Paragraph IV Disputes
- CBI's Annual Summit on Biosimilars and Follow-On Biologics
- ACI's Paragraph IV on Trial: Litigator's Master Class on Paragraph IV Pre-Trial Preparation
- CBI's Pharmaceutical Congress on Paragraph IV Disputes
- FDAnews Audioconference: Navigating the FDA's New 180-Day Generic Marketing Exclusivity Rulings
- Guest Lecturer at the University of Connecticut School of Law
- Collaborating Attorney to the Connecticut Intellectual Property Notes
Professional Activities
- American Bar Association, Intellectual Property, Litigation and Antitrust Sections
- American Intellectual Property Law Association, Co-Chair of the Biologics Subcommittee of the Special Committee on the FDA.
- Connecticut Bar Association
- Connecticut Intellectual Property Law Association
- Hartford County Bar Association
Practice Areas
Industries
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.
News
- Axinn Honored With Litigation Department of the Year
- Chad Landmon Receives University of Connecticut Distinguished Alumni Award
- Chad Landmon Named to Law360's Life Sciences "Rising Star" List
- Axinn Obtains Favorable Decision in FDA Suit
- Axinn Partners Chad A. Landmon and Jeremy C. Lowe Honored as "New Leaders in the Law"
- Axinn, Veltrop & Harkrider Obtains Summary Judgment Victory Against FDA
- Axinn Successful in Protecting Client Alvogen's Entry to Drug Market
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