Patentability of Reach-Through Claims Brian R. Stanton Practice Specialist Technology Center 1600 (703) 308-2801

Slides:



Advertisements
Similar presentations
Examining Pharmaceutical Claims of Immense Scope Gary L. Kunz Supervisory Patent Examiner Art Unit Michael Woodward Training Quality.
Advertisements

Written Description: Antibodies Bennett Celsa TC 1600 QAS
Proteomics Examination Yvonne (Bonnie) Eyler Technology Center 1600 Art Unit 1646 (703)
1 Types of Vaccines and Patentability Considerations Christina Chan Supervisory Primary Examiner Art Unit 1644 Phone:
Utility and Written Description Steve Kunin Deputy Commissioner for Patent Examination Policy Esther Kepplinger Deputy Commissioner for Patent Operations.
More on Restriction Practice Jim Housel SPE, Art Unit 1648 (703)
1 Homology Language Brian R. Stanton Quality Assurance Specialist Technology Center 1600 U.S. Patent and Trademark Office (703)
35 USC §112, First Paragraph, Written Description
INTRODUCTION TO PATENT RIGHTS The Business of Intellectual Property
1 35 U.S.C. § 112, first paragraph and the Wands Analysis Remy Yucel, SPE 1636 (571)
1 35 USC 112, 1 st paragraph enablement Enablement Practice in TC 1600 Deborah Reynolds, SPE
35 U.S.C. 112, Sixth Paragraph MPEP 2181 – 2186 Jean Witz Quality Assurance Specialist Technology Center 1600.
Gene Therapy: Overcoming Enablement Rejections Karen M. Hauda Supervisory Patent Examiner Art Unit 1632 (703)
Proteomics and “Orphan” Receptors Yvonne (Bonnie) Eyler Technology Center 1600 Art Unit 1646 (703)
1 Polymorphs in Pharmaceutical Products Janet Andres TC
“REACH-THROUGH CLAIMS”
1 Biotechnology Partnership Meeting April 17, 2001 James Martinell Senior Level Examiner Technology Center 1600.
Intellectual Property March 4, 2015 Don Keach Director, Intellectual Property Development and Technology Transfer Office Copyright University of Kentucky.
ENABLEMENT / WRITTEN DESCRIPTION PATENT PROSECUTION PRACTICE Presented at: Webb & Co. Rehovot, Israel Date: February 21, 2013 Presented by: Roy D. Gross.
Determination of Obviousness Practice Under the Genus-Species Guidelines and In re Ochiai; In re Brouwer Sreeni Padmanabhan & James Wilson Supervisory.
Antibody Patents in the United States Dan Altman Knobbe Martens Olsen & Bear, LLP Dan Altman Knobbe Martens Olsen & Bear, LLP.
1 Single Nucleotide Polymorphisms (SNP) Gary Jones SPE, Technology Center 1600 (703)
Patent Processing – Examination Issues Patent, Trademark, and Copyright - Law and Policy 5-8 November 2007 Amman, Jordan Global Intellectual Property Academy.
Animals and Transgenesis Peter Paras, Jr.. 2 Overview Introduction — Definitions Types of Transgenic Animals — How they are made Examination of Transgenic.
Biotechnology/Chemical/Pharmaceutical Customer Partnership Topic: Biotechnology/Chemical/Pharmaceutical Customer Partnership Topic: Examining Issues When.
Patent Overview by Jeff Woller. Why have Patents? Patents make some people rich – but, does that seem like something the government should protect? Do.
Issues in Patenting Proteins Jon P Weber, SPE 1657.
By Paul J. Lee. Disclaimer The opinions and views expressed in these materials are not necessarily those of DexCom and reflect only the personal views.
Examination Issues: Immunology Yvonne (Bonnie) Eyler Quality Assurance Specialist Technology Center 1600 USPTO (571)
1 Unity of Invention: Biotech Examples TC1600 Special Program Examiner Julie Burke (571)
1 Intellectual Property Protection for Plants in the United States Anne Marie Grünberg Supervisory Patent Examiner Art Units 1661 and 1638.
RESTRICTING BETWEEN PRODUCT and PROCESS INVENTIONS Bruce Campell Supervisory Patent Examiner Art Unit
Stem Cells Peter Paras, Jr.. 2 Overview Introduction — Definitions Types of Stem Cells — Origin Examination of Stem Cell Claims — Statutes — Sample Claims.
Patenting Antibodies in Europe
Utility Requirement in Japan Makoto Ono, Ph.D. Anderson, Mori & Tomotsune Website:
Examination of Protein Crystallography Applications Kathleen Kerr Bragdon, Ph.D. Supervisory Patent Examiner Art Unit 1656.
Making a Prima Facie Case (e.g. In Polymorph Cases) Bennett Celsa QAS TC 1600 Janet Andres SPE Art Unit 1625 June 12, 2013.
1 ANTICIPATION BY INHERENCY IN PRIOR ART James O. Wilson Supervisory Patent Examiner Technology Center 1600 USPTO (571)
Biotechnology/Chemical/Pharmaceutical Customer Partnership Topic: Biotechnology/Chemical/Pharmaceutical Customer Partnership Topic: Biological Deposits.
Broadening the Scope of the Claims in Gene Therapy Applications Deborah Reynolds Detailee, TCPS
1 Polymorphs in Pharmaceutical Products Janet Andres TC
Impact of Myriad Decisions on Patent Eligibility of Biotechnology Inventions in Australia and the US.
Routine Optimization Jean Witz, tQAS, TC
Enablement in Claims to Therapeutic Treatment Jean Witz tQAS, TC1600.
© 2011 Barnes & Thornburg LLP. All Rights Reserved. This page, and all information on it, is the property of Barnes & Thornburg LLP which may not be reproduced,
Patenting Interfering RNA
U.S. Patent and Trademark Office Technology Center 1600 Michael P. Woodward Unity of Invention: Biotech Examples.
Overcoming Prior Art References Non-Enabling Prior Art References Gary Kunz SPE Art Unit 1616.
1 Written Description Analysis and Capon v. Eshhar Jeffrey Siew Supervisory Patent Examiner AU 1645 USPTO (571)
The Written Description Requirement Why It’s a Good Thing (Seriously) AIPLA Spring Meeting Thursday, May 12, 2011 Amy E. Hamilton Vice President/Deputy.
Patentability Considerations in the 3-D Structure Arts Patentability Considerations in the 3-D Structure Arts Michael P. Woodward Supervisory Patent Examiner.
Trilateral Project WM4 Report on comparative study on Examination Practice Relating to Single Nucleotide Polymorphisms (SNPs) and Haplotypes. Linda S.
The Research Use Exception to Patent Infringement Earlier cases Whittemore v. Cutter 29 F. Cas (C.C.D. Mass. 1813) “It could never have been the.
1 Demystifying the Examination of Stem Cell-Related Inventions Remy Yucel, Ph.D. Supervisory Patent Examiner Technology Center 1600 United States Patent.
Vector Claims in Gene Therapy Applications: In vivo vs. In vitro Utilities Deborah Reynolds SPE GAU
#ACIPIV ACI’s 9 th Annual Paragraph IV Disputes Neal K. Dahiya Senior Counsel – Patent Litigation Bristol-Myers Squibb (Princeton, NJ) Limelight v. Akamai:
How to Claim your Biotech- Based Invention Deborah Reynolds Detailee, TCPS
INTERIM GUIDELINES FOR PATENT SUBJECT MATTER ELIGIBILITY ARDIN MARSCHEL SPE AU 1631 (571)
1 Enablement Issues in Pharmaceutical Claims Joseph K. M c Kane Supervisory Patent Examiner Art Unit Ardin Marschel Supervisory Patent.
Examination Practice in Applications Presenting “Reach-Through Claims” George Elliott Practice Specialist Technology Center 1600
1 Utility Guidelines, Homology Claims and Anti-Sense Molecule Claims Drew Hissong, Ph.D. dhissong*sughrue.com Sughrue Mion, PLLC
© 2015 Waller Lansden Dortch & Davis, LLP. All Rights Reserved. Ready to Patent? Value and Risk Considerations Nicolo Davidson.
Antibody Decisions and Their Compliance with the Written Description Requirement Workgroup
Patenting Biotechnology in Japan and recent hot issues
Processes Which Employ Non-Obvious Products
Ram R. Shukla, Ph.D. SPE AU 1632 & 1634 Technology Center
Patentability Issues and Mechanism Claims
Stem Cells Peter Paras, Jr.
Examination Practice in Applications Presenting “Reach-Through Claims”
Examination Issues: Immunology
Presentation transcript:

Patentability of Reach-Through Claims Brian R. Stanton Practice Specialist Technology Center 1600 (703)

Exemplary Reach Through Situations ä 1. Small molecule per se claim, where the molecule is defined as binding to target but not yet identified (e.g. "A receptor [X] agonist"). ä 2. Method of screening claim: how effectively does this claim protect a small molecule identified in the screen? ä 3. "Functional use" claim: claim is to a method of treating a disease by a compound defined not by its structure but rather by its ability to bind to a target (e.g. "A method of treating disease [Y] by administering a compound which is a receptor [X] agonist."

Major Patentability Issues ä Utility (35 U.S.C. 101) ä See Utility Examination Guidelines ä 66 Fed. Reg (Jan. 5, 2001) ä Written Description (35 U.S.C. 112, 1st para.) ä See Written Description Examination Guidelines ä 66 Fed. Reg ( Jan. 5, 2001) ä Enablement (35 U.S.C. 112, 1st para.) ä Novelty (35 U.S.C. 102) ä Nonobviousness (35 U.S.C. 103)

Receptor Claims ä Major Patentability Issue - Utility ä If applicant shows at least one specific, substantial, and credible utility for the receptor, and other statutory requirements are met, applicant is entitled to a patent on the receptor per se.

Receptor Agonist Claims ä Types of claims at issue: ä “A receptor [X] agonist.” ä “A method of treating disease [Y] by administering a compound which is a receptor [X] agonist.”

Receptor Agonist Claims ä Major Patentability Issue - Written Description ä Generic claim to “A receptor [X] agonist.” unlikely to comply with written description requirement: ä No description of structure of representative number of claimed compounds ä No description of chemical or physical characteristics of representative number of claimed compounds or of function of representative number of claimed compounds (other than binding to identified receptor)  Analogous to Regents of the Univ. of Cal. v. Eli Lilly & Co., 119 F.3d 1559, 43 USPQ2d 1398 (Fed. Cir. 1997) (description of how to obtain compounds not sufficient without description of what the compounds are) ä See also Fiers v. Revel, 984 F.2d 1164, 25 USPQ2d 1601 (Fed. Cir. 1993); In re Ruschig, 379 F.2d 990, 154 USPQ 118 (CCPA 1967)

Receptor Agonist Claims ä Major Patentability Issue - Enablement ä Generic claim to “A receptor [X] agonist.” unlikely to comply with enablement requirement: ä The specification does not usually teach how to make and use the full scope of agonists or antagonists within that genus without undue experimentation. ä Specification usually teaches how to identify compounds, rather than how to make them; specification does not usually teach how to use the full scope of the compounds within the genus without undue experimentation.

Receptor Agonist Claims ä Major Patentability Issue - Enablement ä If a claim to “A receptor [X] agonist” meets the utility, enablement and written description requirements, a claim to “A method of treating disease [Y] by administering a compound which is a receptor [X] agonist” must still be supported by an enabling disclosure. ä Will compound operate as intended without undue experimentation?

More Examples ä Claims: ä 1. An isolated and purified receptor the sequence of which consists of SEQ ID NO: 1. ä 2. A method of identifying an agonist of the receptor of claim 1 comprising: ä preparing a candidate compound, ä contacting a cell which expresses said receptor on its surface with said candidate ä compound, and ä determining whether said candidate compound activates the receptor of claim 1, ä wherein a compound that activates the receptor of claim 1 is an agonist of said re- ceptor. ä 3. An isolated and purified receptor agonist identified by the method of claim 2.

Another Example ä 4. A method for the treatment of disease treatable by the agonist of claim 2,comprising administering to a host in need thereof a therapeutically effective amount of the agonist of claim 3. ä 5. A method for treating a disease treatable by compound X comprising administering to a host in need thereof a therapeutically effective amount of compound X.

Additional Fact Patterns ä Trilateral Web Site Case Studies ä USPTO ä EPO ä JPO ä

Combinatorial Libraries

Combinatorial libraries ä Major Patentability Issue - Utility  Must have a specific, substantial and credible utility for the collection of elements making up the library (e.g., as an extrinsic research tool)  Individual members of the library may not have specific, substantial and credible utilities.  The utility that serves to meet the requirements of 35 U.S.C. §101 relates to the use of the library rather than to the individual members thereof (in the absence of a specific disclosure of a use for an individual member).

Combinatorial Libraries ä Major Patentability Issue - Written Description ä A disclosure of a collection of molecules does not necessarily provide support for a claim drawn to any particular individual member of the collection. ä Possession of a genus does not imply possession of any particular member of genus. ä See Fujikawa v. Wattanasin, 93 F.3d 1559, 39 USPQ2d 1895 (Fed. Cir. 1996) and In re Ruschig, 379 F.2d 990, 154 USPQ 118 (CCPA 1967). ä See also In re Bell, 991 F.2d 781, 26 USPQ2d 1529 (Fed. Cir. 1993) and In re Baird, 16 F.3d 380, 29 USPQ2d 1550 (Fed. Cir. 1994).

Combinatorial Library ä Scope of protection ä Right to exclude others from making, using, selling, offering for sale, or importing the library ä Using a patented library in a screening method for compounds of interest may constitute infringement ä Does a patented claim to a collection of components confer exclusionary rights to the individual members of the collection? ä It is the collection of molecules, not the individual components, that is protected by a claim to a combinatorial library.

Methods of Screening (Combinatorial Libraries; Receptors) ä Major Patentability Issue - Utility ä Requirement met if screening method identifies a ligand which acts upon a receptor so as to effect a specific, substantial, and credible use ä Requirement met if the asserted utility for screening a combinatorial library is specific, substantial, and credible.

Methods of Screening (Combinatorial Libraries; Receptors) ä Scope of Protection ä Claim prevents others from making, using, selling, or offering for sale the claimed screening method. ä A product identified by a screening method is not a product made by a patented process. ä 35 U.S.C. 271(g) includes use, sale, or importation of a product made by a patented process as an act of infringement.

THANK YOU