WSGR logoWSGR logo
WSGR logo
  • Experience
  • People
  • Insights
  • About Us
  • Careers

  • Practice Areas
  • Industries

  • Corporate
  • Intellectual Property
  • Litigation
  • Patents and Innovations
  • Regulatory
  • Technology Transactions

  • Broker-Dealer
  • Capital Markets
  • Corporate Governance
  • Corporate Life Sciences
  • Derivatives
  • Emerging Companies
  • Employee Benefits and Compensation
  • Energy and Climate Solutions
  • Executive Advisory Program
  • Finance and Structured Finance
  • Fund Formation
  • Greater China
  • Investment Adviser
  • Israel
  • Latin America
  • Mergers & Acquisitions
  • Private Equity
  • Public Company Representation
  • Real Estate
  • Restructuring
  • Shareholder Engagement and Activism
  • Tax
  • U.S. Expansion

  • Special Purpose Acquisition Companies (SPACs)

  • Environmental, Social, and Governance

  • Decarbonization Strategies
  • Energy Regulation and Competition
  • Project Development and Transactions
  • Project Finance and Tax Equity
  • Sustainability and Decarbonization
  • Transportation Electrification

  • U.S. Expansion Library and Resources

  • Post-Grant Review
  • Trademark and Advertising

  • Arbitration
  • Board and Internal Investigations
  • Class Action Litigation
  • Commercial Litigation
  • Consumer Litigation
  • Corporate Governance Litigation
  • Employment Litigation
  • Government Investigations
  • Internet Strategy and Litigation
  • Patent Litigation
  • Securities Litigation
  • Supreme Court and Appellate Practice
  • Trade Secret Litigation
  • Trademark and Copyright Litigation
  • Trial
  • White Collar Crime

  • Advertising, Promotions, and Marketing
  • Antitrust and Competition
  • Committee on Foreign Investment in the U.S. (CFIUS)
  • Export Control and Sanctions
  • FCPA and Anti-Corruption
  • FDA Regulatory, Healthcare, and Consumer Products
  • Federal Trade Commission
  • Fintech and Financial Services
  • National Security
  • Payments
  • Privacy and Cybersecurity
  • Strategic Risk and Crisis Management

  • Antitrust and Intellectual Property
  • Antitrust Civil Enforcement
  • Antitrust Compliance and Business Strategy
  • Antitrust Criminal Enforcement
  • Antitrust Merger Clearance
  • Antitrust Litigation
  • European Competition Law
  • Third-Party Merger and Non-Merger Antitrust Representation

  • Anti-Money Laundering
  • Foreign Ownership, Control, or Influence (FOCI)
  • Team Telecom

  • Artificial Intelligence and Machine Learning
  • Aviation
  • Biotech
  • Blockchain and Cryptocurrency
  • Clean Energy
  • Climate and Clean Technologies
  • Communications and Networking
  • Consumer Products and Services
  • Data Storage and Cloud
  • Digital Health
  • Digital Media and Entertainment
  • Electronic Gaming
  • FoodTech and AgTech
  • Fintech and Financial Services
  • Global Generics
  • Internet
  • Life Sciences
  • Medical Devices
  • Mobile Devices
  • Mobility
  • NewSpace
  • Semiconductors
  • Software

  • Offices
  • Events
  • Pro Bono
  • Community
  • Our Diversity
  • Our Values
  • Board of Directors
  • Management Team

  • Austin
  • Beijing
  • Boston
  • Boulder
  • Brussels
  • Century City
  • Hong Kong
  • London
  • Los Angeles
  • New York
  • Palo Alto
  • Salt Lake City
  • San Diego
  • San Francisco
  • Seattle
  • Shanghai
  • SOMA
  • Washington, D.C.
  • Wilmington, DE

  • Law Students + Recent Graduates
  • Experienced Attorneys
  • Patent Agents
  • Professional Staff
  • Alternative Legal Careers
  • Contact Recruiting
Seth C. Silber
Partner
Antitrust and Competition
Washington, D.C.
ssilber@wsgr.com

D202-973-8824

Download vCard
Open PDF
  • Specialized Antitrust Expertise

    Seth focuses on advising clients in the pharmaceutical and healthcare markets, including issues concerning pharmaceutical patent settlements, mergers and acquisitions, and anticompetitive conduct.

  • Deep Antitrust Expertise

    Prior to joining Wilson Sonsini, Seth served for six years at the FTC.

  • Leadership Roles

    Seth is active in the ABA’s Antitrust Section and served as chair of the Health Care and Pharmaceuticals Committee.

Seth Silber is a partner in the firm's Washington, D.C., office, where he focuses on advising clients in the pharmaceutical and healthcare markets, including issues concerning pharmaceutical patent settlements, mergers and acquisitions, and anticompetitive conduct. He regularly represents clients before both the Federal Trade Commission and U.S. Department of Justice.

Seth joined Wilson Sonsini Goodrich & Rosati in September 2006 after serving for six years at the Federal Trade Commission (FTC). During his tenure at the FTC, Seth obtained unique experience and insights into the commission's antitrust activities and enforcement practices, having served at all levels of the commission.

From 2004 to 2006, Seth served as an advisor to former FTC Chairman Jon Leibowitz, advising him on enforcement issues relating to both anticompetitive conduct and mergers affecting various industries, including healthcare, medical devices, media, and oil and gas. He also served as an Assistant to the Bureau Director in the Bureau of Competition. In that role, he reviewed recommendations from the bureau staff on both merger and non-merger matters, with a particular emphasis on pharmaceutical matters.

During his first three years at the FTC, Seth was a staff attorney in the bureau's Health Care Division. He was a lead attorney in FTC v. Schering-Plough and was involved in many of the commission's investigations involving pharmaceutical patent settlements and Orange Book listings. While in the Health Care Division, he also conducted several merger investigations and served as the division's liaison to the Food and Drug Administration.

In his current practice at Wilson Sonsini, Seth regularly counsels clients regarding the antitrust risks posed by pharmaceutical patent settlements and has represented clients in FTC investigations of such settlements. He has also served as lead counsel for several cutting-edge pharmaceutical litigations including litigation concerning pharmaceutical product hopping, REMS systems, and standard setting in the pharmaceutical industry.

Seth is active in the American Bar Association's Antitrust Section. He served as chair of the Health Care and Pharmaceuticals Committee, a position he also held from 2009 to 2012, and from 2016 to 2019. He was appointed in 2012 to serve on the section's governing council and is the lead editor of the first-ever treatise on pharmaceutical antitrust, the Pharmaceutical Industry Antitrust Handbook, which was published by the ABA in 2009.

Prior to joining the FTC, Seth was in private practice at Paul Hastings in Washington, D.C. He also is a part-owner and treasurer of the Fredericksburg Nationals, the Class-A minor league baseball affiliate of the Washington Nationals. Additionally, Seth currently served as the board chair for One World Education, a Washington, D.C.-based nonprofit from 2014 to 2018.

Experience

Seth Silber is a partner in the firm's Washington, D.C., office, where he focuses on advising clients in the pharmaceutical and healthcare markets, including issues concerning pharmaceutical patent settlements, mergers and acquisitions, and anticompetitive conduct. He regularly represents clients before both the Federal Trade Commission and U.S. Department of Justice.

Seth joined Wilson Sonsini Goodrich & Rosati in September 2006 after serving for six years at the Federal Trade Commission (FTC). During his tenure at the FTC, Seth obtained unique experience and insights into the commission's antitrust activities and enforcement practices, having served at all levels of the commission.

From 2004 to 2006, Seth served as an advisor to former FTC Chairman Jon Leibowitz, advising him on enforcement issues relating to both anticompetitive conduct and mergers affecting various industries, including healthcare, medical devices, media, and oil and gas. He also served as an Assistant to the Bureau Director in the Bureau of Competition. In that role, he reviewed recommendations from the bureau staff on both merger and non-merger matters, with a particular emphasis on pharmaceutical matters.

During his first three years at the FTC, Seth was a staff attorney in the bureau's Health Care Division. He was a lead attorney in FTC v. Schering-Plough and was involved in many of the commission's investigations involving pharmaceutical patent settlements and Orange Book listings. While in the Health Care Division, he also conducted several merger investigations and served as the division's liaison to the Food and Drug Administration.

In his current practice at Wilson Sonsini, Seth regularly counsels clients regarding the antitrust risks posed by pharmaceutical patent settlements and has represented clients in FTC investigations of such settlements. He has also served as lead counsel for several cutting-edge pharmaceutical litigations including litigation concerning pharmaceutical product hopping, REMS systems, and standard setting in the pharmaceutical industry.

Seth is active in the American Bar Association's Antitrust Section. He served as chair of the Health Care and Pharmaceuticals Committee, a position he also held from 2009 to 2012, and from 2016 to 2019. He was appointed in 2012 to serve on the section's governing council and is the lead editor of the first-ever treatise on pharmaceutical antitrust, the Pharmaceutical Industry Antitrust Handbook, which was published by the ABA in 2009.

Prior to joining the FTC, Seth was in private practice at Paul Hastings in Washington, D.C. He also is a part-owner and treasurer of the Fredericksburg Nationals, the Class-A minor league baseball affiliate of the Washington Nationals. Additionally, Seth currently served as the board chair for One World Education, a Washington, D.C.-based nonprofit from 2014 to 2018.

Education
  • J.D., The George Washington University Law School, 1997Cum Laude
  • M.A., Johns Hopkins School of Advanced International Studies (SAIS), 1993
  • B.A., Emory University, 1991Cum Laude
Associations and Memberships
  • Chair, Health Care and Pharmaceuticals Committee, Section of Antitrust Law, American Bar Association, 2009-2012, 2016-2019
  • Member, Governing Council, Section of Antitrust Law, American Bar Association (appointed for 2013-2016 term)
Honors
  • Selected for inclusion in the 2016 and 2017 editions of Washington DC Super Lawyers
Admissions
  • Bar of the District of Columbia
Credentials
Education
  • J.D., The George Washington University Law School, 1997Cum Laude
  • M.A., Johns Hopkins School of Advanced International Studies (SAIS), 1993
  • B.A., Emory University, 1991Cum Laude
Associations and Memberships
  • Chair, Health Care and Pharmaceuticals Committee, Section of Antitrust Law, American Bar Association, 2009-2012, 2016-2019
  • Member, Governing Council, Section of Antitrust Law, American Bar Association (appointed for 2013-2016 term)
Honors
  • Selected for inclusion in the 2016 and 2017 editions of Washington DC Super Lawyers
Admissions
  • Bar of the District of Columbia

Select Publications

  • Co-author, "AAM v. Robert Bonta: An End to California Pharmaceutical Legislative Reform?" 32(1) Antitrust and Unfair Competition Law, California Lawyers Association, Spring 2022
  • Co-author with J. Bank, B. Coffman, R. Gray, and N. Mendelsohn, “Fifth Circuit Upholds Federal Trade Commission Ruling in Impax Laboratories, Inc. v. Federal Trade Commission and Grants Substantial Deference to the FTC,” Wilson Sonsini Alert, April 20, 2021
  • Co-author with J. Bank and B. Coffman, "A Return to Republican Antitrust Policies for Pharma," Law360, January 24, 2017
  • Co-author with J. Bank, B. Coffman, and K. Kemp, "Where We Stand On Pharmaceutical Patent Settlements," Law360, October 23, 2015
  • Co-author with V. Norviel, D. Hoffmeister, E. Yin, and C. Andres, "A Look at the Legality Behind Daraprim's Price Spike," Law360, September 30, 2015
  • Co-author with M. Rosman, "DOJ Investigation Into Generic Pharma: You Could Be Next," Law360, March 30, 2015
  • Co-author with J. Lutinski and R. Maddock, "'Good Luck' Post-Actavis: Current State of Play on 'Pay-for-Delay' Settlements," CPI Antitrust Chronicle, November 2014
  • Co-author with V. Rucker and R. Comerford, "Following Up on Follow-On Biologics," Law360, December 2, 2013
  • Co-author with J. Lutinski and C. Armour, "Third Circuit Breathes New Life into FTC Efforts to Block Pharmaceutical Patent Settlements," New Pharma Thinkers, July 27, 2012
  • Co-author with J. Lutinski and R. Taylon, "Abuse of the FDA Citizen Petition Process: Ripe for Antitrust Challenge?" Antitrust Health Care Chronicle, Health Care and Pharmaceuticals Committee, ABA Section of Antitrust Law, Vol. 25, No. 2, January 2012
  • Co-author with K. Kuritz, "Product Switching in the Pharmaceutical Industry: Ripe for Antitrust Scrutiny?" Journal of Generic Medicines, January 12, 2010
  • Lead Editor, Pharmaceutical Antitrust Industry Handbook, ABA Section of Antitrust Law, July 2009
  • Co-author with Susan Creighton, "EC's Preliminary Pharmaceutical Sector Report: An Aggressive Review of Industry Conduct," Global Competition Policy, February 2009
  • "Settlements with Payments to Generics Increase: FTC," Competition Law360, March 28, 2007
  • "FTC Review of Generic Drug Mergers," Journal of Generic Medicines, February 13, 2007


Select Speaking Engagements

Seth speaks frequently on antitrust issues. His prior speaking engagements have focused on FTC enforcement in the pharmaceutical area, authorized generics, pharmacy benefits managers (PBMs), and merger enforcement. Select recent speaking engagements include:

  • "Hot Topics in Antitrust IP: Update on Pay-for-Delay Patent Settlements," American Bar Association Intellectual Property Committee Panel, March 2013
  • "Everything You Need to Know About Pharmaceutical 'Pay-for-Delay' Settlements," American Health Lawyers Association Webinar, December 2011
  • Moderator for Post-Conference Workshop on "Responding to an FTC Patent Settlement Investigation," ACI Sixth Annual In-House Counsel Forum on Pharmaceutical Antitrust, May 2011
  • "Clearing the Way for Biosimilars: New Complexities Around Competition and Consumer Harm," American Bar Association Antitrust Section Teleseminar, February 2011
  • Conference Co-chair, Fifth Annual In-House Counsel Forum on Pharmaceutical Antitrust, February 17-18, 2010
  • "Setting the Framework: Antitrust Review of Reverse-Payment Patent Settlements," Bates White Healthcare Law and Economics Workshop, October 29, 2009
  • "Pharmaceutical Antitrust Initiatives and Developments in the U.S. and Abroad," American Conference Institute, July 29, 2009
  • "Mitigating Antitrust Concerns When Settling Paragraph IV Disputes," American Conference Institute's Conference on Paragraph IV Litigation, April 29, 2009
  • Conference Co-chair, Fourth Annual In-House Counsel Forum on Pharmaceutical Antitrust, May 20-21, 2008
  • "Merger Review and the Pharmaceutical Industry," Law Seminars International Conference on Pharmaceutical Antitrust, April 24, 2008
  • "Pharmaceutical Antitrust Issues in the United States," European Pharmaceutical Law Forum, October 2007
  • "Antitrust Issues Relating to Generic Competition," ABA/AHLA Conference on Antitrust in Health Care, September 18, 2007
  • Conference Co-chair (and Panelist on Authorized Generics), Third Annual In-House Counsel Forum on Pharmaceutical Antitrust, May 15-16, 2007
  • "Biotech Mergers: FTC Review and Guidance," Biotechnology 2007 Conference, January 29, 2007
  • "Authorized Generics: Their Role in the Marketplace, and the FTC Study," ABA Health Care Committee Panel, September 2006
  • Keynote Address, "FTC Initiatives to Promote Pharmaceutical Competition," American Conference Institute's Conference on Maximizing Pharmaceutical Patent Life Cycles, June 14, 2006
  • Panel Participant on Authorized Generics, Second Annual In-House Counsel's Forum on Pharmaceutical Antitrust, April 24, 2006
  • Presentation on Authorized Generics, In-House Counsel's Forum on Pharmaceutical Antitrust, May 24, 2005
  • "FTC's Actions Affecting Generic Drug Markets," Generic Pharmaceutical Association, 2005 Legal Symposium, May 18, 2005
  • "Update on FTC's Views and Findings on the PBM Market," Second Annual Forum on Minimizing Legal Risk in Pharmaceutical Benefit Management, April 18, 2005
  • "FTC Enforcement Priorities," 4th Annual Generic Drug Forum, November 17, 2004
  • "FTC's PBM Activities," Forum on Minimizing Legal Risk in Pharmaceutical Benefit Management, March 22, 2003
Insights

Select Publications

  • Co-author, "AAM v. Robert Bonta: An End to California Pharmaceutical Legislative Reform?" 32(1) Antitrust and Unfair Competition Law, California Lawyers Association, Spring 2022
  • Co-author with J. Bank, B. Coffman, R. Gray, and N. Mendelsohn, “Fifth Circuit Upholds Federal Trade Commission Ruling in Impax Laboratories, Inc. v. Federal Trade Commission and Grants Substantial Deference to the FTC,” Wilson Sonsini Alert, April 20, 2021
  • Co-author with J. Bank and B. Coffman, "A Return to Republican Antitrust Policies for Pharma," Law360, January 24, 2017
  • Co-author with J. Bank, B. Coffman, and K. Kemp, "Where We Stand On Pharmaceutical Patent Settlements," Law360, October 23, 2015
  • Co-author with V. Norviel, D. Hoffmeister, E. Yin, and C. Andres, "A Look at the Legality Behind Daraprim's Price Spike," Law360, September 30, 2015
  • Co-author with M. Rosman, "DOJ Investigation Into Generic Pharma: You Could Be Next," Law360, March 30, 2015
  • Co-author with J. Lutinski and R. Maddock, "'Good Luck' Post-Actavis: Current State of Play on 'Pay-for-Delay' Settlements," CPI Antitrust Chronicle, November 2014
  • Co-author with V. Rucker and R. Comerford, "Following Up on Follow-On Biologics," Law360, December 2, 2013
  • Co-author with J. Lutinski and C. Armour, "Third Circuit Breathes New Life into FTC Efforts to Block Pharmaceutical Patent Settlements," New Pharma Thinkers, July 27, 2012
  • Co-author with J. Lutinski and R. Taylon, "Abuse of the FDA Citizen Petition Process: Ripe for Antitrust Challenge?" Antitrust Health Care Chronicle, Health Care and Pharmaceuticals Committee, ABA Section of Antitrust Law, Vol. 25, No. 2, January 2012
  • Co-author with K. Kuritz, "Product Switching in the Pharmaceutical Industry: Ripe for Antitrust Scrutiny?" Journal of Generic Medicines, January 12, 2010
  • Lead Editor, Pharmaceutical Antitrust Industry Handbook, ABA Section of Antitrust Law, July 2009
  • Co-author with Susan Creighton, "EC's Preliminary Pharmaceutical Sector Report: An Aggressive Review of Industry Conduct," Global Competition Policy, February 2009
  • "Settlements with Payments to Generics Increase: FTC," Competition Law360, March 28, 2007
  • "FTC Review of Generic Drug Mergers," Journal of Generic Medicines, February 13, 2007


Select Speaking Engagements

Seth speaks frequently on antitrust issues. His prior speaking engagements have focused on FTC enforcement in the pharmaceutical area, authorized generics, pharmacy benefits managers (PBMs), and merger enforcement. Select recent speaking engagements include:

  • "Hot Topics in Antitrust IP: Update on Pay-for-Delay Patent Settlements," American Bar Association Intellectual Property Committee Panel, March 2013
  • "Everything You Need to Know About Pharmaceutical 'Pay-for-Delay' Settlements," American Health Lawyers Association Webinar, December 2011
  • Moderator for Post-Conference Workshop on "Responding to an FTC Patent Settlement Investigation," ACI Sixth Annual In-House Counsel Forum on Pharmaceutical Antitrust, May 2011
  • "Clearing the Way for Biosimilars: New Complexities Around Competition and Consumer Harm," American Bar Association Antitrust Section Teleseminar, February 2011
  • Conference Co-chair, Fifth Annual In-House Counsel Forum on Pharmaceutical Antitrust, February 17-18, 2010
  • "Setting the Framework: Antitrust Review of Reverse-Payment Patent Settlements," Bates White Healthcare Law and Economics Workshop, October 29, 2009
  • "Pharmaceutical Antitrust Initiatives and Developments in the U.S. and Abroad," American Conference Institute, July 29, 2009
  • "Mitigating Antitrust Concerns When Settling Paragraph IV Disputes," American Conference Institute's Conference on Paragraph IV Litigation, April 29, 2009
  • Conference Co-chair, Fourth Annual In-House Counsel Forum on Pharmaceutical Antitrust, May 20-21, 2008
  • "Merger Review and the Pharmaceutical Industry," Law Seminars International Conference on Pharmaceutical Antitrust, April 24, 2008
  • "Pharmaceutical Antitrust Issues in the United States," European Pharmaceutical Law Forum, October 2007
  • "Antitrust Issues Relating to Generic Competition," ABA/AHLA Conference on Antitrust in Health Care, September 18, 2007
  • Conference Co-chair (and Panelist on Authorized Generics), Third Annual In-House Counsel Forum on Pharmaceutical Antitrust, May 15-16, 2007
  • "Biotech Mergers: FTC Review and Guidance," Biotechnology 2007 Conference, January 29, 2007
  • "Authorized Generics: Their Role in the Marketplace, and the FTC Study," ABA Health Care Committee Panel, September 2006
  • Keynote Address, "FTC Initiatives to Promote Pharmaceutical Competition," American Conference Institute's Conference on Maximizing Pharmaceutical Patent Life Cycles, June 14, 2006
  • Panel Participant on Authorized Generics, Second Annual In-House Counsel's Forum on Pharmaceutical Antitrust, April 24, 2006
  • Presentation on Authorized Generics, In-House Counsel's Forum on Pharmaceutical Antitrust, May 24, 2005
  • "FTC's Actions Affecting Generic Drug Markets," Generic Pharmaceutical Association, 2005 Legal Symposium, May 18, 2005
  • "Update on FTC's Views and Findings on the PBM Market," Second Annual Forum on Minimizing Legal Risk in Pharmaceutical Benefit Management, April 18, 2005
  • "FTC Enforcement Priorities," 4th Annual Generic Drug Forum, November 17, 2004
  • "FTC's PBM Activities," Forum on Minimizing Legal Risk in Pharmaceutical Benefit Management, March 22, 2003
Focus Areas
  • Antitrust Civil Enforcement
  • Antitrust Compliance and Business Strategy
  • Antitrust Litigation
  • Antitrust Merger Clearance
  • Antitrust and Competition
  • Antitrust and Intellectual Property
  • Global Generics
  • Privacy and Cybersecurity
  • Third-Party Merger and Non-Merger Antitrust Representation
Recent Insights
Alerts
Jury Finds Gilead and Teva Did Not Engage in an Anticompetitive Pay-for-Delay Scheme for HIV Drugs
On June 30, 2023, a jury in the Northern District of California found Gilead and Teva not liable in a trial accusing the companies of engaging in an illegal reverse payment to delay generic versions of two HIV drugs, Truvada (emtricitabine/tenofovir) and Atripla (efavirenz-/-emtricitabine-/-tenofovir). Following a five-week trial and two days of deliberations, the jury found that the plaintiffs failed to show that: 1) Gilead had market power within a market that included Truvada and/or Atripla, and 2) Gilead made a reverse payment to Teva to delay the entry of generic competition.1 This case marks the third jury verdict in favor of defendants in reverse-payment cases since the 2013 FTC v. Actavis decision—there have been no verdicts for plaintiffs.2
Learn More
News Articles
Wilson Sonsini and Attorneys Recognized in 2022 Edition of LMG Life Sciences
LMG Life Sciences recognized several Wilson Sonsini practices and 16 of its attorneys in the 2022 edition of its guide, which identifies and ranks the leading law firms and individuals in the life sciences industry.
Learn More
View All
Recent Events
Affiliated Programs
Life Sciences Antitrust Conference
As we proceed through 2021, the spotlight on antitrust activity in the life sciences industry shines brighter than ever. For several years, state and federal antitrust enforcers in the U.S. and even international antitrust and competition authorities have been watching the life sciences industry closely for anticompetitive activity. The Biden Administration is now forming its new competition policy and there is pending antitrust legislation which will unquestionably affect the life sciences industries. At the same time, the U.S. DOJ has just confirmed that they are developing new policies to prevent patents from being used as tools for anticompetitive practices, a recent series of criminal antitrust investigations have been brought by federal and state authorities alleging generic price fixing collusion, and a novel multinational task force has just been put in place to examine the anticompetitive impact of life sciences M+A activity. All of these new changes are raising life sciences antitrust concerns to an all-time high, and could significantly increase the volume of litigation for IP and antitrust trial lawyers and their clients.
Learn More
  • people
  • insights
  • about us
  • careers
  • Binder
  • Alumni
  • Mailing List Signup
  • Employee Login
  • Client FTP Portal
  • Privacy Policy
  • Terms of Use
  • Accessibility
WSGR logo
Twitter
LinkedIn
Facebook
Instagram
Youtube
Copyright © 2023 Wilson Sonsini Goodrich & Rosati. All Rights Reserved.