DOCSLIB.ORG

Pascal Soriot Executive Director, Chief Executive Officer

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Pascal Soriot Executive Director, Chief Executive Officer Pascal Soriot Executive Director, Chief Executive Officer Pascal joined AstraZeneca as an Executive Director and Chief Executive Officer on 1 October 2012. A French national, Pascal joined AstraZeneca from Roche AG where he served as Chief Operating Officer of the company’s pharmaceuticals division since 2010. Prior to that Pascal was Chief Executive Officer of Genentech, where he was credited with leading the successful merger between the San Francisco- based biologics business and Roche. Pascal joined the pharmaceutical industry in 1986 and has worked in senior management roles in the US, Asia and Europe. Luke Miels Executive Vice President Global Portfolio & Product Strategy (GPPS) Luke started his career in 1995 with AZ in Australia where he was successively a Sales Representative and Product Manager for Plendil and Diprivan. He joined Aventis in late 2000 as Marketing and Strategic Planning Manager in Australia before being appointed Country Manager for New Zealand in 2002 and subsequently Thailand the following year. He then transferred to the USA to lead the Analytics and Commercial Effectiveness function of Aventis US. Following the Sanofi-Aventis merger he led the integration office in the US and was appointed Vice President of Sales for Metabolism at the conclusion of the merger. In 2006 he moved to Basel to join Roche as Head of Metabolism for Global Marketing. Three years later he was appointed to the role of Regional VP Asia Pacific for the Pharmaceuticals Division and joined the Leadership Team of the Pharmaceuticals Division, initially based in Shanghai and more recently in Singapore. Luke is married with three children and has an MBA from the Macquarie University, Sydney and a BSc Biology from Flinders University in Adelaide. Mark Mallon Executive Vice President, International Mark Mallon is responsible for the growth and performance of AstraZeneca’s International region, which predominantly includes AstraZeneca’s commercial businesses in Asia Pacific, Russia, Latin America, the Middle East and Africa. Most recently, Mark served as Regional Vice President for Asia Pacific where he was accountable for the growth and performance of the AstraZeneca business in 14 markets. While in this role Mark has also served as President of AstraZeneca China, responsible for the company’s overall operations in China and Hong Kong. Previously, Mark led the marketing, sales and commercial operations for AstraZeneca K. K. (Japan). Since joining AstraZeneca in 1994, Mark has held a number of additional leadership roles, Including Marketing Company President of the AstraZeneca Italian subsidiary company and Vice President of Marketing and Sales Operations of AstraZeneca’s US business. While in the US, Mark also was a Board Member for the Christiana Care Network, one of the the largest healthcare networks on the East Coast. Mark received a Bachelor of Science degree in Chemical Engineering from the University of Pennsylvania and an MBA in Marketing and Finance from the Wharton School of Business. He is based in Shanghai. Dr Zhengbin (Bing) Yao Head of MedImmune Respiratory, Inflammation & Autoimmune (RIA) iMed Dr. Zhengbin (Bing) Yao joined MedImmune in 2010 as Senior Vice President and head of the Respiratory, Inflammation, and Immunology (RIA) Innovative Medicines unit. In this role, he leads a cross-functional team dedicated to the development of therapeutic area strategy and advancement of the company’s RIA biologics portfolio. RIA’s focus is to develop biologics as potentially new and exciting treatments for asthma, COPD, idiopathic pulmonary fibrosis, systemic lupus erythematosus, rheumatoid arthritis, and other related diseases. Bing has 20 years of experience in the leading biotechnology and pharmaceutical companies. Bing previously led the project team leaders’ group for immunology, central nervous system, virology, and metabolism for Genentech research and early development. Prior to Genentech, he served as Vice President of Research, Acting Head of Clinical, and Corporate Officer for Tanox, and held roles of increasing responsibilities at Aventis, and Amgen. Bing received his doctorate in microbiology and immunology from the University of Iowa and did his post-doctoral research at Immunex. Bing has authored more than 50 peer reviewed publications and holds over 20 patents and patent applications. Elisabeth Björk M.D PhD Vice President, Head CVMD GMed & Mölndal Site Lead Elisabeth is the VP CVMD GMed – the Head of late phase Cardiovascular and Metabolic development unit within AZ. She is leading the development activities across the AZ late phase cardiovascular (mainly Brilinta, Crestor and Epanova), diabetes (mainly Onglyza, Forxiga, Byetta, Bydureon and combinations) and CKD (roxadustat and tenapenaror in development) portfolio. Prior to taking on this role in June 2012, Elisabeth was Global Product VP for dapagliflozin (approved as Forxiga in Europe and many other countries, including Australia, and as Farxiga in the US), and led the development of this first-in-class drug in partnership with Bristol Myers Squibb. She has also been involved in the delivery of key late phase CVMD and GI projects like Crestor, Nexium, Onglyza, Brilinta and others. She led the team that delivered several CV outcomes studies for Crestor (CORONA, JUPITER, AURORA). Elisabeth has a passion for patients and science, with a special focus on CV outcomes trials, as well as for developing people and teams and inspire them to achievements they did not think were possible. Elisabeth herself is on a constant learning curve and enjoys doing things she has never done before. Elisabeth is an endocrinologist by training and an associate professor of medicine at Uppsala University, and was Head of the Diabetes and Endocrinology Unit at the University Hospital, Uppsala, where she spent 15 years in clinical practice and diabetes research, before joining AZ in 2002. Susan Galbraith Head of Innovative Medicines Oncology iMed Susan Galbraith trained as a Clinical Oncologist in the United Kingdom. She studied Medicine at Manchester and Cambridge Universities. She was admitted to Membership of the Royal College of Physicians in 1992, and then trained in Clinical Oncology in London. She gained Fellowship of the Royal College of Radiologists in 1997. She then completed a PhD at the University of London involving translational work on a vascular-targeting agent. Susan joined the Clinical Discovery Oncology group at Bristol-Myers Squibb in 2001. Susan was closely involved in the in-licensing of ipilimumab from Medarex, elotuzumab from PDL, the acquisitions of Adnexus and Medarex and research collaborations with Exelixis. She held increasing levels of responsibility becoming VP for Oncology and Immunology Early Development, and then latterly taking on responsibility for the Clinical Biomarker team. Susan joined AZ in September 2010, as Head of the Oncology iMed responsible for Oncology Discovery and Early Development to Proof of Concept Mohammed M. Dar, M.D. Vice President, Oncology Clinical Development Dr. Dar is the Head of Clinical Development at MedImmune for the Oncology TA. In this role, he is accountable for overseeing the development and execution of all studies involving MedImmune’s clinical stage assets for oncology. Dr. Dar joined MedImmune in January of 2013 in his current role. Prior to joining MedImmune, Dr. Dar spent nearly 10 years at GlaxoSmithKline in roles of increasing responsibility focused on early clinical development in oncology. During this time, Dr. Dar led the early clinical development of numerous small molecule kinase inhibitors and large molecules. This included 10 First Time in Human studies, multiple Phase 2 Proof-of-Concepts studies and a variety of clinical pharmacology studies. He was also involved in the successful NDA submission and approval of Votrient for renal cell carcinoma. Dr. Dar received his Bachelors in Chemistry from the University of North Carolina at Chapel Hill and M.D. from Duke University School of Medicine. He completed his residency in Internal Medicine at Duke University and went on to complete a Fellowship in Hematology and Oncology at the National Institutes of Health. Rachel Humphrey, M.D. Head of Immuno-oncology GMed, AZ Rachel Humphrey, MD, currently heads the late stage Immuno-Oncology department at AZ and is the former Executive VP and Chief Medical Officer for Mirati Therapeutics in San Diego. She may be best known for her work at BMS where she led the clinical development of the CTLA-4 antagonist monoclonal antibody Yervoy, the first immunotherapy to demonstrate survival in patients with metastatic melanoma, including 10-year survival in a subset of patients. As well as supervising a range of alliance and in- licensing projects and new drug filings at BMS, she has also worked in a range of senior clinical development and strategy roles at Bayer Pharmaceuticals, supervising the development of Nexavar, among other anti-cancer agents. Previously, Rachel was a Staff Physician Scientist at the National Cancer Institute where she completed her Clinical Oncology Fellowship. Board Certified in Internal Medicine with a residency at John Hopkins Hospital, she was educated at Harvard and the Case Western Reserve University (CWRU) Medical School in Cleveland. She has authored more than 20 publications, and an extensive number of abstracts. Outside of work, Rachel has produced, directed and performed in community theatre productions and is the lead singer of The Checkpoints, a blues band made up of leaders in
Load more

Recommended publications
  • Medical Research Council
    OFFICIAL MEDICAL RESEARCH COUNCIL 03 Should not be viewed by CEO due to Author: Sam Bartholomew Conflict of interest Should not be viewed by deputy CEO due to Conflict of interest Trade Union Side access: In part Minutes of the Council meeting held at the Chelsea Harbour Hotel on 7 March 2018 Present: Council Head Office staff Mr Donald Brydon (Chair) Ms Sam Bartholomew Sir John Savill (CEO) Professor David Lomas Professor Jonathan Bisson Dr Rob Buckle Dr John Brown Mr Hugh Dunlop Professor Doreen Cantrell Dr Declan Mulkeen Professor Chris Day Dr Tony Peatfield Professor Dame Janet Finch Mrs Helen Page Professor John Iredale Dr Rachel Quinn Mr Richard Murley Dr Frances Rawle Baroness Onora O’Neill Ms Pauline Mullin (item 9a&b only) Dr Mene Pangalos Professor Irene Tracey Guests – item 8 Dr Pauline Williams Nick Lemoine, Chair MRF Trust Angela Hind, CEO MRF Observers Ms Jenny Dibden (BEIS) Professor Fiona Watt, MRC Executive Chair Designate 1. Announcements Mr Brydon welcomed members to the last meeting of the MRC Council as currently constituted, prior to the transition to UK Research and Innovation. He introduced Professor Fiona Watt, MRC Executive Chair Designate, and Professor Jonathan Bisson who was attending his first meeting since being appointed as a Council member in the summer. He offered congratulations to those MRC-associated people whose achievements had been recognised in the New Year’s Honours: • Sir Keith Peters Sir Keith, lately Regius Professor of Physic at the University of Cambridge, was appointed Knight Grand Cross of the Order of the British Empire (GBE) for services to 1 OFFICIAL the advancement of medical science.
    [Show full text]
  • Analyst Report
    ASTRAZENECA PLC AZN LN Sector: Healthcare Industry: EUROPEAN EQUITY Pharmaceuticals RESEARCH I SHORT POSITION MEMO Market Unattractive position with a limited scope REDUCE Capitalization: €58,920.65 m With negative sales growth of 6 %, a loss of 23% in earnings per share (01/28/2014) compared to 2012 and a last quarter negative operating and net income, AstraZeneca is facing a challenge to recover a decent sales and profitability level in the Pharmaceutical industry. Country: GB FY 2013 ISIN: GB0009895292 In Millions Est FY 2012 FY 2011 FY 2010 FY 2009 Index: STOXX 600 12/31/2013 12/31/2012 12/31/2011 12/31/2010 12/31/2009 Market: London Stock Shares issued 1,257.00 1,261.00 1,361.00 1,438.00 1,448.00 Dividend yield (%) Exchange 2.26 1.99 1.77 1.48 Price 43.07 36.94 36.25 34.73 32.78 Revenue 20,462.28 21,768.38 24,151.51 25,129.22 23,588.60 oji Growth %, YoY -6.00 -9.87 -3.89 6.53 Source : Bloomberg # of employees: 53,500 CEO: Pascal Soriot AZN AVG P/E 17.38 21.32 P/S 3.05 3.56 P/EBITDA 8.04 11.11 P/B 3.45 5.72 2Y RV GR -2% OPE CF -5% ANALYST: Valentin ROUSSEL [email protected] The stock is outperforming the Legal & General Global Health and Pharmaceuticals Index since December (+24.6% in one year,Source +17.8% : Bloomberg in 5 years). The price should reflect a reaction to pipeline new introductions and investors looking beyond the patent cliff.
    [Show full text]
  • Pfizer Inr 235 East 42Nd Street New York
    Pfizer Inr 235 East 42nd Street New York. !W 10007-5755 March 25,2008 Steven Reynolds Director U.S. Nuclear Regulatory Commission Division of Nuclear Materials Safety 2443 Warrenville Road, STE 210 Lisle, IL 60532-4352 -Re: Parent Company Guarantee for Pharmacia Corporation (Chesterfield, MO and St. Louis, MO) Dear Mr. Reynolds: I am the Chief Executive Officer of Pfizer Inc. located at 235 East 42"d Street in New York, NY 10017. This letter is in support of this firm's use of the financial test to demonstrate financial assurance, as specified in 10 CFR Part 30. I hereby certify that Pfizer Inc. is currently a going concern, and that it possesses positive tangible net worth in the amount of $23,129,000,000. This firm is required to file a Form 10K with the U.S. Securities and Exchange Commission for the latest fiscal year. The fiscal year of this firm ends on December 3 1. I hereby certify that the content of this letter is true and correct to the best of my knowledge. panof the Board C ief Executive Officer Pfizer lnr 235 East 42nd Street New York, NY 10007-5755 March 25. 2008 Steven Reynolds Director U.S. Nuclear Regulatory Coinmission Division of Nuclear Material Safet) 2443 Warrenville Road STE 2 IO Lisle. IL 60532-4352 -Re: Financial Assurance Demonstration for Pharmacia Corporation (Chesterfield, MO and St. Louis, MO) Dear Mr. Reynolds: I am the chief financial officer of Pfizer Inc., 235 East 42'ld Street, New York. New York 10017, a corporation. This letter is in support of this firm's use of the parent company guarantee financial test to demonstrate financial assurance, as specified in IO CFR Part 30.
    [Show full text]
  • Research and Development at the University of Maryland Baltimore
    RESEARCH AND DEVELOPMENT AT THE UNIVERSITY OF MARYLAND BALTIMORE FISCAL YEAR 2002 ANNUAL REPORT ANNUAL REPORT TABLE OF CONTENTS Overview 1 Extramural Funding at UMB 1 Office of Research and Development Outcomes 2 Success by School 6 Areas of Strength 13 Technology Commercialization 14 New Initiatives 19 Appendixes 20 David J. Ramsay, DM, DPhil President James L. Hughes Vice President, Research & Development www.ord.umaryland.edu RESEARCH AND DEVELOPMENT AT THE UNIVERSITY OF MARYLAND BALTIMORE ANNUAL REPORT FY 02 RESEARCH AND DEVELOPMENT AT THE UNIVERSITY OF MARYLAND BALTIMORE FISCAL YEAR 2002 ANNUAL REPORT OVERVIEW The University of Maryland Baltimore reached a milestone number in extramural funding in FY 02: $305.3 million. The research conducted on campus and the hundreds of projects funded from federal, state and local governments and the private sector demonstrate UMB’s ever-increasing contribution to the life sciences and health care research fields. As an economic engine for Maryland, UMB provides access to millions of dollars of research to the business community. The commercial potential for much of this work is being actively patented and licensed. Summary of Success Principal Investigators with Awards: 617 Principal Investigators with $1 million Plus in Awards: 44 Funding Applications: 2,274 Funding Awards: 1,673 Total Dollar Amount of Extramural Funding: $305.3 Million Total Dollar Amount of Extramural Funding through ORD: $250 Million % of Total Extramural Funding: 82% Volume of Federal Awards: $142.7 Million NIH Funding Amount: $127.2 Million % of Indirect Costs: 22.8% EXTRAMURAL FUNDING AT UMB Support for extramural funding at the UMB campus has tripled in the last eight years.
    [Show full text]
  • 2014.10.22-110Cv00528-Pfizer-Etal
    IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF DELAWARE PFIZER INC., PHARMACIA & UPJOHN ) COMPANY, PHARMACIA & UP JOHN ) COMPANY LLC, SUGEN, INC., C.P .. ) PHARMACEUTICALS INTERNATIONAL ) C.V., PFIZER PHARMACEUTICALS LLC, ) C.A. No. 10-528-GMS and PF PRISM C.V., ) ) Plaintiffs, ) ) v. ) ) MYLAN PHARMACEUTICALS INC., ) ) Defendant. ) _______________________________ ) MEMORANDUM I. INTRODUCTION In this patent infringement action, plaintiffs Pfizer Inc., Pharmacia & Upjohn Company, Pharmacia & Upjohn Company LLC, Sugen, Inc., C.P. Pharmaceuticals International C.V., Pfizer Pharmaceuticals LLC, and PF Prism C.V. (collectively, "Pfizer") allege that pharmaceutical products proposed by defendant Mylan Pharmaceuticals Inc. ("Mylan") infringe the asserted claims of the patents-in-suit. (D.I. 1.) The court held a four-day bench trial in this matter on November 26 through November 29, 2012. (D.I. 148-151.) Presently before the court are the parties' post-trial proposed findings of fact and conclusions of law concerning the validity of the patents-in-suit, specifically whether the asserted claims are invalid as obvious under 35 U.S.C. § 103. (D.I. 152, 153.) Pursuant to Federal Rule of Civil Procedure 52( a), and after having considered the entire record in this case and the applicable law, the court concludes that: (1) all asserted claims ofthe patents-in-suit are not invalid due to obviousness; and (2) Pfizer's Rule 52(c) motion is granted, and Mylan's Rule 52( c) motion is denied. These findings of fact and conclusions oflaw are set forth in further detail below. II. FINDINGS OF FACT 1 A. The Parties 1. Plaintiff Pfizer Inc.
    [Show full text]
  • Optimizing Binding Kinetics in Medicinal Chemistry: Facts Or Fantasy?
    Optimizing Binding Kinetics in Medicinal Chemistry: facts or fantasy? ‡ -Gon /RT kon e -G‡ /RT ‡ off ΔG on koff e -ΔGd/RT Kd e koff /kon P + L ‡ ΔG off ΔGd PL Gerhard Müller Ex-Head of Med Chem Mercachem, Nijmegen, NL Binding coordinate 11 The topic is hot, complex, and I am just an end-user & controversial “You can’t optimize koff, and you don’t need to optimize koff, you simply need to optimize Kd ! ” Head Med Chem, (top-5 Pharma), West Coast, US, Jan 2016 Optimizing Binding Kinetics in Medicinal Chemistry: facts or fantasy? ‡ -Gon /RT kon e -G‡ /RT ‡ off ΔG on koff e -ΔGd/RT Kd e koff /kon P + L ‡ ΔG off ΔGd PL Gerhard Müller Chief Scientific Officer Gotham Therapeutics, New YorkBinding coordinate 2 confidential Streetlight effect in medicinal chemistry Top-heavy distributions, rich-get-richer mechanisms 5% / 75% J. Med. Chem., 54 ,6405–6416 (2011) Vertex Pharmaceuticals, US J. Org. Chem. 73, 4443-4451 (2008) MW clogP shape clogP flatness Fsp3 flatland J. Med. Chem., 58, 2390−2405 (2015) para meta ortho J. Med. Chem., 59, 4443–4458 (2016) 3 Cheminformatics Analysis – Kinase Family Ligand and target promiscuity (ChEMBL21) Hu, Kunimoto, Bajorath Chemical Biology & Drug Design, 89, 834-845 (2017) quantitative kinome coverage 270 kinases with high-confidence data Top-10 kinases (45% of human kinome still unexplored) VEGFR2 TK 2239 erbB1 TK 1814 22.537 distinct IC50 values p38a CMGC 1509 9191 distinct scaffolds HGFR TK 1411 31.873 kinase-inhibitor combinations PI3a lipid 844 erbB-2 TK 768 GSK3b CMGC 743 SRC TK 709 Chk1 CAMK 693
    [Show full text]
  • SU14813: a Novel Multiple Receptor Tyrosine Kinase Inhibitor with Potent Antiangiogenic and Antitumor Activity
    1774 SU14813: a novel multiple receptor tyrosine kinase inhibitor with potent antiangiogenic and antitumor activity Shem Patyna,1 A.Douglas Laird, 3 Dirk B.Mendel, 5 KIT, and FLT3. In cellular assays, SU14813inhibited ligand- Anne-Marie O’Farrell,2 Chris Liang,6 dependent and ligand-independent proliferation, migration, Huiping Guan,8 Tomas Vojkovsky,6 Stefan Vasile,7 and survival of endothelial cells and/or tumor cells express- B Xueyan Wang,9 Jeffrey Chen,1 Maren Grazzini,1 ing these targets. SU14813inhibited VEGFR-2, PDGFR- , Cheng Y.Yang, 10 Joshua O˝.Haznedar, 5 and FLT3phosphorylation in xenograft tumors in a dose- 4 1 and time-dependent fashion. The plasma concentration Juthamas Sukbuntherng, Wei-Zhu Zhong, in vivo 2 1 required for target inhibition was estimated to be Julie M.Cherrington, and Dana Hu-Lowe 100 to 200 ng/mL. Used as monotherapy, SU14813 1Pfizer Global Research and Development; 2Phenomix Corp., exhibited broad and potent antitumor activity resulting in San Diego, California; 3Exelixis, Inc.; 4Celera Genomics, Inc., regression, growth arrest, or substantially reduced South San Francisco, California; 5Chiron Corp., Emeryville, growth of various established xenografts derived from 6 7 California; The Scripps Research Institute; The Burnham human or rat tumor cell lines. Treatment in combination Institute, La Jolla, California; 8AstraZeneca PLC, Waltham, Massachusetts; 9Metabolex, Inc., Hayward, California; and with docetaxel significantly enhanced both the inhibition 10Gilead Sciences, Inc., Foster City, California of primary tumor growth and the survival of the tumor- bearing mice compared with administration of either agent alone. In summary, SU14813inhibited target RTK Abstract activity in vivo in association with reduction in angio- Receptor tyrosine kinases (RTK), such as vascular endo- genesis, target RTK-mediated proliferation, and survival thelial growth factor receptor (VEGFR), platelet-derived of tumor cells, leading to broad and potent antitumor growth factor receptor (PDGFR), stem cell factor receptor efficacy.
    [Show full text]
  • Documenting the Biotechnology Industry in the San Francisco Bay Area
    Documenting the Biotechnology Industry In the San Francisco Bay Area Robin L. Chandler Head, Archives and Special Collections UCSF Library and Center for Knowledge Management 1997 1 Table of Contents Project Goals……………………………………………………………………….p. 3 Participants Interviewed………………………………………………………….p. 4 I. Documenting Biotechnology in the San Francisco Bay Area……………..p. 5 The Emergence of An Industry Developments at the University of California since the mid-1970s Developments in Biotech Companies since mid-1970s Collaborations between Universities and Biotech Companies University Training Programs Preparing Students for Careers in the Biotechnology Industry II. Appraisal Guidelines for Records Generated by Scientists in the University and the Biotechnology Industry………………………. p. 33 Why Preserve the Records of Biotechnology? Research Records to Preserve Records Management at the University of California Records Keeping at Biotech Companies III. Collecting and Preserving Records in Biotechnology…………………….p. 48 Potential Users of Biotechnology Archives Approaches to Documenting the Field of Biotechnology Project Recommendations 2 Project Goals The University of California, San Francisco (UCSF) Library & Center for Knowledge Management and the Bancroft Library at the University of California, Berkeley (UCB) are collaborating in a year-long project beginning in December 1996 to document the impact of biotechnology in the Bay Area. The collaborative effort is focused upon the development of an archival collecting model for the field of biotechnology to acquire original papers, manuscripts and records from selected individuals, organizations and corporations as well as coordinating with the effort to capture oral history interviews with many biotechnology pioneers. This project combines the strengths of the existing UCSF Biotechnology Archives and the UCB Program in the History of the Biological Sciences and Biotechnology and will contribute to an overall picture of the growth and impact of biotechnology in the Bay Area.
    [Show full text]
  • Scientific Insights in a Pandemic COVID-19 National Core Studies Symposium 24 June 2021
    Scientific Insights in a Pandemic COVID-19 National Core Studies Symposium 24 June 2021 Agenda Session title and speaker 09:00 Opening keynote: A year of accelerated science and impacts Jeremy Farrar, Wellcome Trust 09.10 UK COVID Science, the public and the media • Fiona Fox, Science Media Centre • Chris Monk, public representative 09.20 Scientific impact on the NHS and patients Mark Toshner, Cambridge University Hospitals NHS Foundation Trust 09.30 Plenary keynote: What we have learned from COVID? Patrick Vallance, Chief Scientific Advisor UK Government 09.50 National Core Studies – impact and future potential • Transmission and environment – Andrew Curran • Longitudinal health and wellbeing – Nish Chaturvedi and Jonathan Sterne • Immunity – Paul Moss • Epidemiology and Surveillance – Ian Diamond • Vaccines Trials Infrastructure – Divya Chadha Manek • Therapeutics Trials Infrastructure – Patrick Chinnery • Data and Connectivity – Andrew Morris Chaired by Anne Johnson Q&A 11.10 Break 11.20 Lightning talks - Scientific Impact of UK COVID science 11.20 Group 1 Group 2 • Anne-Marie Docherty, University of • Dinesh Aggarwal, University of Edinburgh Cambridge • Marion Mafham, Nuffield Department of • Helen Parry, NIHR Population Health, University of Oxford • Joshua Elliott, Imperial College London • Muzz Hanifa, Newcastle University • William Hulme, Oxford DataLab • Cameron Razieh, University of Leicester Q&A Q&A 12.10 Preparing for the next pandemic • Mene Pangalos, AstraZeneca • Gabriel Leung, University of Hong Kong • Lynda Stuart, Bill & Melinda Gates Foundation • Further speakers TBC 12:35 International Guest lecture - Opportunities for global collaborative open science Keynote speaker TBC Fireside chat with Ottoline Leyser, Chief Executive, UK Research and Innovation 12:55 Closing remarks Patrick Vallance, Government Chief Scientific Adviser 13:00 End .
    [Show full text]
  • Pfizer, Inc., Letter of Support for Parent
    Ptizer Inc 235 East 42nd Street New York, NY 1OOl7-5755 March 25,2008 Steven Reynolds Director U.S.Nuclear Regulatory Commission Division of Nuclear Material Safety 2443 Warrenville Road, STE 2 10 Lisle, IL 60532-4352 -Re: Parent Company Guarantee for Pharmacia & Upjohn Co. (Kalamazoo, MI) Dear Mr. Reynolds: I am the Chief Executive Officer of Pfizer Inc. located at 235 East 42ndStreet in New York, NY 10017. This letter is in support of this firm's use of the financial test to demonstrate financial assurance, as specified in 10 CFR Part 30. I hereby certify that Pfizer Inc. is currently a going concern, and that it possesses positive tangible net worth in the amount of $23,129,000,000. This firm is required to file a Form 10K with the U.S. Securities and Exchange Commission for the latest fiscal year. The fiscal year of this firm ends on December 3 1. I hereby certify that the content of this letter is true and correct to the best of my knowledge. ofthe ~oard Chief Executive Officer RECEIVED MAR 2 8 2008 .' . Pfizer Inr 235 East 42nd Street New lork. NY 10007-5755 March 25, 2008 Steven Reynolds Director U .S . N uc I ear Reg u la t ory C om m i ss i on Division of Nuclear Material Safet) 2443 Warrenville Road, STE 2 IO Lisle, IL 60532-4352 -Re: Financial Assurance for Pharmacia & Upjohn Company LLC (Kalainazoo, MI) Dear Mr. Reynolds: 1 am the chief financial officer of Pfizer Inc.. 235 East 42'IdStreet, New York.
    [Show full text]
  • Astrazeneca 17Th January 2013 Attractive Risk-Reward As New CEO Comes in Healthcare Fair Value 3440P Vs
    INDEPENDENT RESEARCH AstraZeneca 17th January 2013 Attractive risk-reward as new CEO comes in Healthcare Fair Value 3440p vs. 2860p (price 3,042p) BUY vs. NEUTRAL Bloomberg AZN LN Among the big names in the pharmaceutical industry, AstraZeneca is Reuters AZN.L obviously one of the few which carries in principle one of the most 12-month High / Low (p) 3,112 / 2,591 significant upsides considering its current valuation, provided the new Market capitalisation (GBPm) 37,921 Enterprise Value (BG estimates GBPm) 39,062 CEO, Pascal Soriot, is able not only to present a comprehensive and Avg. 6m daily volume ('000 shares) 2,247 clear strategy but also to package his speech in an attractive manner Free Float 100% for the investment community to jump in as early as the beginning of 3y EPS CAGR [2012-2015] -1.2% Gearing (12/11) 8% 2013. Dividend yields (12/12e) 5.72% On 31 January 2013, Pascal Soriot is expected to present his initial YE December 12/11 12/12e 12/13e 12/14e thoughts about how to drive AstraZeneca forward and which strategy to Revenue (USDm) 33,591 28,081 27,524 27,251 EBIT(USDm) 12,795 7,921 7,818 8,334 implement. Since he took over as CEO on 1 October 2012, he has spent Basic EPS (USD) 7.33 4.81 4.58 5.04 much time meeting people within the group and also key shareholders to Core EPS (USD) 7.72 6.71 6.13 6.33 EV/Sales 1.9x 2.2x 2.2x 2.0x make the best possible assessment of the situation and to hear their EV/EBITDA 4.1x 6.0x 5.6x 5.0x expectations and hopes before presenting a roadmap.
    [Show full text]
  • Astrazeneca Plc
    6/15/2020 AstraZeneca - Wikipedia AstraZeneca AstraZeneca plc[3] is a British-Swedish multinational pharmaceutical and biopharmaceutical company with its global AstraZeneca plc headquarters in Cambridge, England.[4] Its R&D is concentrated in Cambridge, Gaithersburg, Maryland, and Mölndal in Sweden.[5] AstraZeneca has a portfolio of products for major disease areas including cancer, cardiovascular, gastrointestinal, infection, Type Public limited neuroscience, respiratory and inflammation.[6] company Traded as LSE: AZN (https:// The company was founded in 1999 through the merger of the www.londonstocke [7][8] Swedish Astra AB and the British Zeneca Group (itself formed xchange.com/exch by the demerger of the pharmaceutical operations of Imperial ange/searchengin Chemical Industries in 1993). Since the merger it has been among e/search.html?lang the world's largest pharmaceutical companies and has made =en&x=0&y=0&q= numerous corporate acquisitions, including Cambridge Antibody AZN) Technology (in 2006), MedImmune (in 2007), Spirogen (in 2013) NYSE: AZN (http and Definiens (by MedImmune in 2014). s://www.nyse.com/ quote/XNYS:AZN) AstraZeneca has a primary listing on the London Stock Exchange Nasdaq and is a constituent of the FTSE 100 Index. It has secondary listings Stockholm: AZN (ht on the New York Stock Exchange and the OMX exchange. tp://www.nasdaqom xnordic.com/aktier/ microsite?language Contents Id=1&Instrument=S SE3524) History FTSE 100 2000–06 Component 2007–12: The patent cliff and subsequent acquisitions ISIN GB0009895292 2013
    [Show full text]