Annual Report on Form 20-F 2018
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Overview of Ftc Antitrust Actions in Pharmaceutical Services and Products
OVERVIEW OF FTC ANTITRUST ACTIONS IN PHARMACEUTICAL SERVICES AND PRODUCTS Health Care Division Bureau of Competition Federal Trade Commission Washington D.C. 20580 Markus H. Meier Assistant Director Bradley S. Albert Deputy Assistant Director Saralisa C. Brau Deputy Assistant Director September 2009 TABLE OF CONTENTS Page I. INTRODUCTION. ........................................................... 1 II. CONDUCT INVOLVING PHARMACEUTICAL SERVICES AND PRODUCTS. 3 A. Monopolization. ...................................................... 3 B. Agreements Not to Compete. ............................................ 8 C. Agreements on Price or Price-Related Terms. 14 D. Agreements to Obstruct Innovative Forms of Health Care Delivery or Financing. 20 E. Illegal Tying and Other Arrangements. .................................... 20 III. PHARMACEUTICAL MERGERS. ........................................... 20 A. Horizontal Mergers Between Direct Competitors. 20 B. Potential Competition Mergers. ......................................... 44 C. Innovation Market Mergers. ............................................ 47 D. Vertical Mergers...................................................... 49 IV. INDUSTRY GUIDANCE STATEMENTS...................................... 50 A. Advisory Opinions. ................................................... 50 B. Citizen Petition to the Food and Drug Administration. 51 V. AMICUS BRIEFS. ......................................................... 51 VI. INDICES. ............................................................ -
Robert J. Desalvo Papers Business Combinations in the Cosmetic and Pharmaceutical Industries 1944
Robert J. DeSalvo Papers Business Combinations in the Cosmetic and Pharmaceutical Industries 1944 - 1990 Collection #107 Abstract Robert J. DeSalvo’s research focused on business combinations (acquisitions, mergers, and joint ventures in the cosmetic and pharmaceutical industries. This topic was the basis for his master’s thesis in pharmacy administration at the University of Pittsburgh and continued as a life-long interest. This collection consists of two series of notebooks that Dr. DeSalvo developed to record relevant business combinations. The first series records acquisitions, proposed acquisitions, mergers, and joint ventures for the period of 1944 –1990 in an alphabetical arrangement. The information on these entries is cumulative so that the history of an organization is collected in one place. The second series of notebooks is arranged in chronological blocks. The information is arranged alphabetically by the name of the acquirer. The name of the acquired (merged), type of combination (acquisition, proposed acquisition, joint venture) and the date is also provided. The information is cross-referenced between the two series so that the researcher can approach the information by the name of the parent company or chronologically. Dr. DeSalvo used this resource for many of his publications as well as his master’s thesis. A copy of these publications and his thesis make up the remainder of the collection. Donor Gift of Barbara DeSalvo, 2000 Biography Robert James DeSalvo was born on July 20, 1933 in Toledo, OH. He died on January 23, 1993 in Cincinnati, OH. DeSalvo graduated from high school in Toledo and attended pharmacy school at the University of Toledo where he received his B.S. -
Sanofi-Aventis
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 20-F (Mark One) ‘ REGISTRATION STATEMENT PURSUANT TO SECTION 12(b) OR (g) OF THE SECURITIES EXCHANGE ACT OF 1934 OR È ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2010 OR ‘ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 OR ‘ SHELL COMPANY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 Date of event requiring this shell company report ................... For the transition period from to Commission File Number: 001-31368 Sanofi-Aventis (Exact name of registrant as specified in its charter) N/A (Translation of registrant’s name into English) France (Jurisdiction of incorporation or organization) 174, avenue de France, 75013 Paris, France (Address of principal executive offices) Karen Linehan, Senior Vice President Legal Affairs and General Counsel 174, avenue de France, 75013 Paris, France. Fax: 011 + 33 1 53 77 43 03. Tel: 011 + 33 1 53 77 40 00 (Name, Telephone, E-mail and/or Facsimile number and Address of Company Contact Person) Securities registered or to be registered pursuant to Section 12(b) of the Act: Name of each exchange Title of each class: on which registered: American Depositary Shares, each New York Stock Exchange representing one half of one ordinary share, par value €2 per share Ordinary shares, par value €2 per share New York Stock Exchange (for listing purposes only) Securities registered pursuant to Section 12(g) of the Act: American Depositary Shares, each representing one quarter of a Participating Share Series A, par value €70.89 per share (removed from listing and registration on the New York Stock Exchange effective July 31, 1995). -
Annual Report on Form 20-F 2018
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 20-F (Mark One) ☐ REGISTRATION STATEMENT PURSUANT TO SECTION 12(b) OR (g) OF THE SECURITIES EXCHANGE ACT OF 1934 or ☒ ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2018 Or ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 Or ☐ SHELL COMPANY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 Date of event requiring this shell company report For the transition period from to Commission File Number: 001-31368 Sanofi (Exact name of registrant as specified in its charter) N/A (Translation of registrant’s name into English) France (Jurisdiction of incorporation or organization) 54, Rue La Boétie, 75008 Paris, France (Address of principal executive offices) Karen Linehan, Executive Vice President Legal Affairs and General Counsel 54, Rue La Boétie, 75008 Paris, France. Fax: 011 + 33 1 53 77 43 03. Tel: 011 + 33 1 53 77 40 00 (Name, Telephone, E-mail and/or Facsimile number and Address of Company Contact Person) Securities registered or to be registered pursuant to Section 12(b) of the Act: Title of each class: Name of each exchange on which registered: American Depositary Shares, each representing one half of one ordinary share, par value€2 per share NASDAQ Global Select Market Ordinary shares, par value€2 per share NASDAQ Global Select Market* Contingent Value Rights NASDAQ Global Market Securities registered pursuant to Section 12(g) of the Act: None The number of outstanding shares of each of the issuer’s classes of capital or common stock as of December 31, 2018 was: Ordinary shares: 1,245,454,385 Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. -
FORM 20-F 2015 UNITED STATES SECURITIES and EXCHANGE COMMISSION Washington, D.C
FORM 20-F 2015 UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 20-F (Mark One) ‘ REGISTRATION STATEMENT PURSUANT TO SECTION 12(b) OR (g) OF THE SECURITIES EXCHANGE ACT OF 1934 or È ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2015 Or ‘ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 Or ‘ SHELL COMPANY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 Date of event requiring this shell company report For the transition period from to Commission File Number: 001-31368 Sanofi (Exact name of registrant as specified in its charter) N/A (Translation of registrant’s name into English) France (Jurisdiction of incorporation or organization) 54, Rue La Boétie, 75008 Paris, France (Address of principal executive offices) Karen Linehan, Executive Vice President Legal Affairs and General Counsel 54, Rue La Boétie, 75008 Paris, France. Fax: 011 + 33 1 53 77 43 03. Tel: 011 + 33 1 53 77 40 00 (Name, Telephone, E-mail and/or Facsimile number and Address of Company Contact Person) Securities registered or to be registered pursuant to Section 12(b) of the Act: Title of each class: Name of each exchange on which registered: American Depositary Shares, each representing one half of one ordinary share, par value €2 per share New York Stock Exchange Ordinary shares, par value €2 per share New York Stock Exchange (for listing purposes only) Contingent Value Rights NASDAQ Global Market Securities registered pursuant to Section 12(g) of the Act: None The number of outstanding shares of each of the issuer’s classes of capital or common stock as of December 31, 2015 was: Ordinary shares: 1,305,696,759 Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. -
Reckitt Benckiser Set to Acquire SSL for £2.54Bn
OTC30-07-10p1.qxd 28/7/10 05:55 Page 1 30 July 2010 COMPANY NEWS 2 Reckitt Benckiser set to Novartis makes OTC gains 2 thanks to pain Sigma wants better offer from Aspen 3 J&J loses US$187mn 4 acquire SSL for £2.54bn off US OTC sales GSK’s Alli suffers European decline 6 eckitt Benckiser has agreed to buy SSL Reckitt Benckiser said it would assess the GlaxoSmithKline snaps up 7 Futura’s pain relief product RInternational for £2.54 billion (C3.03 “growth potential and strategic fit” of SSL’s billion) in a deal that will add the Durex and smaller brands. A spokesperson for Reckitt Swedish pharmacists to 8 open Boots pharmacies Scholl brands to its global health and per- Benckiser told OTC bulletin that it was too Celesio takes DocMorris to Italy 9 sonal care portfolio. early to say whether the company would make Bart Becht, chief executive officer of Reck- any divestments. Domestic growth lifts Omega 10 itt Benckiser,said the two brands would bring SSL’s OTC portfolio includes Earex ear GENERAL NEWS 12 the company’s total ‘Powerbrands’ to 19. drops, Full Marks head-lice treatments, Meltus He pointed out the deal would be a “step cough medicines, Mister Baby baby products, Heads of agencies consult 12 change” for Reckitt Benckiser’s global Health and Syndol and Cuprofen pain relievers. on their five-year strategy & Personal Care division. Health & Personal The deal – which has been agreed by the Member states decline to give 13 Care’s annual sales would increase by more boards of both companies – will see Reckitt okay to general health claims than a third to approximately £2.8 billion, he Benckiser pay £11.63 in cash per SSL share ASA has concerns about Diabetone 15 said, adding that the enlarged division would with a further entitlement to a dividend of £0.08 German associations slam 16 represent a third of the group’s total turnover. -
Financial Services
Half-year edition DEAL DRIVERS North amerIca The comprehensive review of mergers and acquisitions in the North America region. 2010 Published by: In association with: When we’re sharing highly confidential information, how can we be sure our documents are secure?” We thought of that. Protect your company and your partners by using a secure, online virtual data room. Nothing in due diligence is more imperative than protecting the security of critical information and keeping buyers anonymous. That’s why so many companies entrust their most valuable information to Merrill DataSite ®. Merrill DataSite is the first virtual data room provider to respond to customers’ and the industry’s need to provide the highest level of security by obtaining ISO/IEC 27001:2005 security certification. Our track record speaks for itself. To date, we have empowered more than 1.6 million unique visitors to perform electronic due diligence on thousands of transactions totaling trillions of dollars in asset value. In every instance, we’ve protected our clients’ data. At Merril DataSite, we believe in sharing ideas and best practices that assist companies in expanding and capturing new opportunities. To download our FREE industry survey reports please visit the Merrill DataSite Knowledge Center at www.datasite.com. MERRILL DATASITE® datasite.com 3 Contents Foreword 04 Technology, Media & Telecom (TMT) 30 New England 58 Heat Chart 05 Life Sciences & Healthcare 34 Latin America 62 All Sectors 06 Canada 38 About Merrill Corporation 66 Financial Services 14 West 42 Merrill Corporation Contacts 68 Industrials, Manufacturing Midwest 46 Notes 69 & Engineering 18 South 50 About Remark 70 Energy, Mining, Oil & Gas 22 Mid-Atlantic 54 Consumer 26 About mergermArket mergermarket is an independent mergers and acquisitions (m&a) intelligence service with an unrivalled network of dedicated m&a journalists based in 62 locations across the americas, europe, asia- Pacific, them iddle-east and africa. -
Late-Breaking 2020 VMX Program FINAL.Pdf
LATE BREAKING RESEARCH New systematic therapies and trends in cutaneous melanoma deaths among US Caucasians, 1986 – 2016 Until recently, metastatic cutaneous melanoma was a nearly incurable cancer. However, the development of new, highly effective therapies and trends toward the diagnoses of earlier stage tumors described in recent publications suggest that population-level improvements in mortality have occurred. We reviewed melanoma incidence and mortality among Caucasians (the group most affected by melanoma) using the National Cancer Institute’s Surveillance, Epidemiology and End Results (SEER) dataset. From 1986 to 2016, incidence rates increased by 108% with an (Annual Percent Change (APC) = 2.7% (95% CI: 2.5 – 2.9). Between 1986 and 2013, overall mortality rates increased by 7.5%. Beginning in 2011, ten new treatments for metastatic melanoma were approved by the FDA. From 2013 to 2016, overall mortality for the general population decreased by 17.9% with an APC = -6.24% (95% CI: -8.7 – -3.7). The sharpest declines were among men ≥50 (APC -8.25%; 95% CI: -12.2 – -4.1) starting in 2014, and women ≥50 (APC -5.8%; 95% CI: -8.9 – -2.5) starting in 2013. This recent, multi-year decline is the largest and most sustained improvement in melanoma mortality ever observed, and is unprecedented in cancer medicine. We conclude that the introduction of new therapies for metastatic melanoma is associated with a significant reduction in population-level mortality. Author(s): David Polsky, MD, PhD, The Ronald O. Perelman Department of Dermatology; Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, NY; Juliana Berk-Krauss, MD, The State University of New York Downstate Medical Center, Brooklyn, NY; The Ronald O. -
Overview of Ftc Actions in Pharmaceutical Products and Distribution*
OVERVIEW OF FTC ACTIONS IN PHARMACEUTICAL PRODUCTS AND DISTRIBUTION* Health Care Division Bureau of Competition Federal Trade Commission Washington D.C. 20580 Markus H. Meier Assistant Director Bradley S. Albert Deputy Assistant Director Kara Monahan Deputy Assistant Director June 2019 * Actions involving health care services and products are contained in a separate document, Overview of FTC Actions in Health Care Services and Products. Information about advisory opinions in the health care and pharmaceutical sectors is contained in the document Topic and Yearly Indices of Health Care Antitrust Advisory Opinions by Commission and by Staff. TABLE OF CONTENTS I. INTRODUCTION ...............................................................................................................1 II. CONDUCT INVOLVING PHARMACEUTICAL PRODUCTS .......................................3 A. Monopolization ........................................................................................................3 B. Agreements Not to Compete ..................................................................................14 III. CONDUCT INVOLVING PHARMACEUTICAL DISTRIBUTION ..............................19 A. Monopolization ......................................................................................................19 B. Agreements on Price and Price-Related Terms .....................................................20 C. Agreements to Obstruct Innovative Forms of Health Care Delivery or Financing................................................................................................................26 -
Trade Marks Journal No: 1862 , 13/08/2018 CORRIGENDA
Trade Marks Journal No: 1862 , 13/08/2018 CORRIGENDA APPL CORRIGENDA DESCRIPTION NO 1467308 1467308 - (1387-0) 2109500 2109500 - (1853-0) TYPOGRAPHICAL ERROR IN THE SPECIFICATION OF GOODS IS CORRECTED TO READ AS "Pharmaceutical and veterinary preparations; sanitary preparations for medical purposes; dietetic substances adapted for medical use, food for babies; plasters, materials for dressings; material for stopping teeth, dental wax; disinfectants; preparations for destroying vermin; fungicide; herbicides." IN CLASS 05. -
Technology Sourcing Through Acquisitions: Evidence from the US Drug Industry
Journal of International Business Studies (2005) 36, 89–103 & 2005 Palgrave Macmillan Ltd. All rights reserved 0047-2506 $30.00 www.jibs.net Technology sourcing through acquisitions: evidence from the US drug industry 1 Karen Ruckman Abstract There were a large number of US drug company takeovers in the 1990s by 1Simon Fraser University, Burnaby, British both foreign and domestic acquirers. Observation of the absolute difference Columbia, Canada between target and acquirer R&D intensity suggests there is no difference between foreign and domestic technology-sourcing patterns. However, a firm- Correspondence: level estimation of the acquirers’ choice of targets reveals that foreign and Dr Karen Ruckman, Simon Fraser University, domestic acquirers differ with respect to the relationship between target and 8888 University Drive, Burnaby, British Columbia, Canada V5A 1S6. acquirer R&D intensity. Foreign acquirers with low R&D intensity choose Tel: þ 1 604 291 3708; targets with high R&D intensities, which suggests technology sourcing as a Fax: þ 1 604 291 4920; motivation. Domestic acquirers prefer targets with high R&D intensities the E-mail: [email protected] higher their own R&D intensity, which suggests a synergy story. Journal of International Business Studies (2005) 36, 89–103. doi:10.1057/palgrave.jibs.8400110 Keywords: acquisitions; technology transfer; research and development Introduction Acquisitions of companies in high-technology industries are a common and important method of gaining access to technology. Between 1993 and 1999, there were 93 acquisitions in the US drug industry (biotechnology1 and pharmaceutical industries com- bined), which had an average of 330 firms each year during the time period. -
MEET SANOFI Management Forward Looking Statements
MEET SANOFI Management Forward Looking Statements This presentation contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking statements are generally identified by the words "expects", "anticipates", "believes", "intends", "estimates", "plans" and similar expressions. Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing, decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological application that may be filed for any