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Champion Brands to My Wife, Mercy the ‘Made in Germany’ Champion Brands Nation Branding, Innovation and World Export Leadership
The ‘Made in Germany’ Champion Brands To my wife, Mercy The ‘Made in Germany’ Champion Brands Nation Branding, Innovation and World Export Leadership UGESH A. JOSEPH First published 2013 by Gower Publishing Published 2016 by Routledge 2 Park Square, Milton Park, Abingdon, Oxon OX14 4RN 711 Third Avenue, New York, NY 10017, USA Routledge is an imprint of the Taylor & Francis Group, an informa business Copyright © Ugesh A. Joseph 2013 Ugesh A. Joseph has asserted his right under the Copyright, Designs and Patents Act, 1988, to be identified as the author of this work. Gower Applied Business Research Our programme provides leaders, practitioners, scholars and researchers with thought provoking, cutting edge books that combine conceptual insights, interdisciplinary rigour and practical relevance in key areas of business and management. All rights reserved. No part of this book may be reprinted or reproduced or utilised in any form or by any electronic, mechanical, or other means, now known or hereafter invented, including photocopying and recording, or in any information storage or retrieval system, without permission in writing from the publishers. Notice: Product or corporate names may be trademarks or registered trademarks, and are used only for identification and explanation without intent to infringe. British Library Cataloguing in Publication Data A catalogue record for this book is available from the British Library. The Library of Congress has cataloged the printed edition as follows: Joseph, Ugesh A. The ‘Made in Germany’ champion brands: nation branding, innovation and world export leadership / by Ugesh A. Joseph. pages cm Includes bibliographical references and index. ISBN 978-1-4094-6646-8 (hardback: alk. -
R&D Update Call 2020
R&D Update Call 2020 Luciano Rossetti, Global Head of Research & Development Rehan Verjee, Head of the Global Innovative Medicine Franchises & President of EMD Serono Joern-Peter Halle, Head of Research Klaus Edvardsen, Head of Oncology Development September 25, 2020 Disclaimer Publication of Merck KGaA, Darmstadt, Germany. In the United States and Canada the group of companies affiliated with Merck KGaA, Darmstadt, Germany operates under individual business names (EMD Serono, Millipore Sigma, EMD Performance Materials). To reflect such fact and to avoid any misconceptions of the reader of the publication certain logos, terms and business descriptions of the publication have been substituted or additional descriptions have been added. This version of the publication, therefore, slightly deviates from the otherwise identical version of the publication provided outside the United States and Canada. 2 Disclaimer Cautionary Note Regarding Forward-Looking Statements and financial indicators This communication may include “forward-looking statements.” Statements that include words such as “anticipate,” “expect,” “should,” “would,” “intend,” “plan,” “project,” “seek,” “believe,” “will,” and other words of similar meaning in connection with future events or future operating or financial performance are often used to identify forward-looking statements. All statements in this communication, other than those relating to historical information or current conditions, are forward-looking statements. We intend these forward-looking statements to be covered by the safe harbor provisions for forward-looking statements in the Private Securities Litigation Reform Act of 1995. These forward-looking statements are subject to a number of risks and uncertainties, many of which are beyond control of Merck KGaA, Darmstadt, Germany, which could cause actual results to differ materially from such statements. -
Low Discontinuation Rate and Side-Effect Burden After Switching to Cladribine Tablets: Canadian Experience from the Advevatm Patient Support Program
Low discontinuation rate and side-effect burden after switching to cladribine tablets: Canadian experience from the advevaTM patient support program Jiwon Oh1, Paul Giacomini2, Virginia Devonshire3, Fraser Clift4, Caroline Lemieux5, Meritxell Sabidó6, Arthur Allignol6, Mark S. Freedman7 1Division of Neurology, Department of Medicine, St Michael's Hospital, University of Toronto, Toronto, ON, Canada. 2Department of Neurology, Montreal Neurological Institute, McGill University, Montreal, QC, Canada. 3Division of Neurology, Department of Medicine, University of British Columbia MS/NMO Center, Vancouver, BC, Canada. 4Department of Neurology, Memorial University of Newfoundland, St. John's, Newfoundland and Labrador, Canada. 5EMD Inc., Mississauga, Canada; a business of Merck KGaA, Darmstadt, Germany. 6Global Epidemiology Department, Merck KGaA, Darmstadt, Germany. 7Department of Medicine, Division of Neurology, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada. ACTRIMS-ECTRIMS 2020 Virtual Congress | 11-13 September DISCLOSURES This study was sponsored by EMD Inc., Canada (a business of Merck KGaA, Darmstadt, Germany), who reviewed and provided feedback on the poster. The authors had full control of the poster, and provided their final approval of all content Jiwon Oh has received research support from Biogen-Idec, Roche, and EMD Serono and has received personal compensation for consulting from EMD Serono, Sanofi-Genzyme, Biogen-Idec, Roche, Celgene, and Novartis Paul Giacomini has received research or educational -
Adding Cetuximab to Paclitaxel and Carboplatin for First-Line
www.nature.com/bjc ARTICLE Clinical Study Adding cetuximab to paclitaxel and carboplatin for first-line treatment of carcinoma of unknown primary (CUP): results of the Phase 2 AIO trial PACET-CUP Gunnar Folprecht1, Karolin Trautmann1, Alexander Stein2, Gerdt Huebner3, Michael Stahl4, Stefan Kasper5, Albrecht Kretzschmar6, Claus-Henning Köhne7, Viktor Grünwald 8,9, Ralf-Dieter Hofheinz10, Katharina Schütte1, Harald Löffler11, Carsten Bokemeyer2, Alwin Krämer12 and Arbeitsgemeinschaft Internistische Onkologie (AIO) - CUP Group BACKGROUND: Patients with carcinoma of unknown primary (CUP) have a dismal prognosis, even when treated with multi-agent chemotherapy. We hypothesised that adding the epidermal growth-factor receptor (EGFR) inhibitor cetuximab to standard first-line chemotherapy with paclitaxel and carboplatin would improve PFS and RR in unfavourable CUP. METHODS: This open-labelled, multicentre Phase 2 study included patients with unfavourable, untreated adeno- or undifferentiated CUP. Patients were randomised to receive either paclitaxel/carboplatin (group A) or paclitaxel/carboplatin plus cetuximab (group B) every 3 weeks for a maximum of 6 cycles followed by cetuximab maintenance in group B. The primary endpoint was PFS in the two groups. Secondary endpoints were RR, toxicity and overall survival (OS). RESULTS: One-hundred-and-fifty patients were randomised (group A = 72, group B = 78). The median PFS and OS for all patients were 3.8 and 8.1 months (95% confidence interval (CI): 2.9–4.8 and 6.8–9.5). There was no significant difference in PFS (3.7 vs 4.6 months, HR 0.98) or OS (8.1 vs 7.4, HR 1.1) between the two treatment groups. -
Merck Exits Insulin Glargine Market, Remains Committed to Biosimilars
19 October 2018 No. 3927 Scripscrip.pharmaintelligence.informa.com Pharma intelligence | informa The follow-on product, developed with partner Samsung Bioepis Co. Ltd., would have been the third Lantus version on the market in the US behind Sanofi’s original product and Eli Lilly & Co.’s Basaglar, which launched in December 2015 after Lilly reached a patent settlement agreement with Sanofi. Both copies are technically approved under the 505(b)(2) regulatory pathway for NDAs, rather than through the biosimilar pathway, based on the way insulin is cate- gorized at the FDA, but the agency is recat- egorizing insulins as biologics in a transition that will go into effect in 2020. ANOTHER SETBACK FOR BIOSIMILARS? Merck’s decision could be another sign that the US biosimilar market isn’t living up to the early hype. A handful of initial lackluster Merck Exits Insulin Glargine Market, launches have raised questions about the commercial potential for biosimilars in the US in the near-term. Even FDA Commis- Remains Committed To Biosimilars sioner Scott Gottlieb has expressed concern JESSICA MERRILL [email protected] that slow launches could lead drug manu- facturers to curtail biosimilar R&D. (Also see erck & Co. Inc. has decided that The decision is surprising since the prod- “FDA’s Gottlieb: ‘Pricing And Reimbursement it will not commercialize its own uct was tentatively approved by the FDA in Mischief’ Holding Back Biosimilar Market” - Mversion of Sanofi’s Lantus (insulin July 2017, though it had not launched. Ten- Scrip, 7 Mar, 2018.) glargine) in the US, even though the prod- tative approval is used by the FDA when a Momenta announced Oct. -
Affectis-Merck Press Release 080611 English
News Release June 8, 2011 Affectis Pharmaceuticals and Merck Serono Announce an Agreement to Develop Oral Drugs for Neurodegenerative Diseases • Merck Serono to develop compounds from Affectis targeting P2X7 receptors Martinsried, Germany, June 8, 2011 – Affectis Pharmaceuticals AG, Munich, Germany, today announced that an exclusive licensing agreement was signed with Merck Serono, a division of Merck KGaA, Darmstadt, Germany, for the development and commercialization of oral compounds targeting P2X7 receptors. These receptors are believed to be involved in neuroinflammation observed in some neurodegenerative diseases. Under the terms of the agreement, Merck Serono will have worldwide exclusive rights to develop and commercialize selected compounds. The contract also includes a research collaboration focusing on P2X7 antagonist optimization. Affectis will receive EUR 2.4 million in upfront payment and research funding, and could receive up to EUR 277 million in milestones for the first three products to come out of the collaboration, as well as undisclosed royalties. “This agreement validates Affectis’ strategy to focus on small molecules that potentially target the neuroinflammatory aspect of some neurodegenerative diseases. We look forward to collaborating with Merck Serono, an industry leader in the field,” said Dr. Manfred Ruediger, Chief Executive Officer, Affectis Pharmaceuticals. Dr. Michael Boes, Chief Scientist Officer of Affectis, further commented, “Affectis’ chemistry expertise puts special emphasis on brain penetration, which supports our development of oral P2X7 antagonists for the potential treatment of central nervous system diseases”. 1 “We are pleased to announce this collaboration with Affectis Pharmaceuticals, a company with robust experience in drug discovery in the central nervous system area,” said Dr. -
News Release Phone +49 6151-72 7144
Your Contact Phyllis Carter News Release Phone +49 6151-72 7144 June 28, 2007 European Union CHMP Recommends Approval of New Formulation of Multiple Sclerosis Treatment Rebif® (interferon beta-1a) • New formulation of Rebif® designed to improve tolerability and immunogenicity profiles Darmstadt, June 28, 2007 – Merck KGaA announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMEA) has issued a positive opinion recommending marketing authorization of a new formulation of Rebif® (interferon beta-1a) for the treatment of relapsing multiple sclerosis (MS). The new formulation of Rebif® was developed by the Merck Serono division to increase treatment benefit by improving injection tolerability and reducing immunogenicity. “The CHMP recommendation for the new formulation of Rebif® is encouraging news for patients with multiple sclerosis in Europe,” said Anthony Coombs, Head of the Global Therapeutic Area Neurology at Merck Serono. “While Rebif® is well established in the treatment of multiple sclerosis, this new formulation demonstrates our commitment to the further development of products that enhance the convenience and tolerability of treatments for patients with multiple sclerosis.” The CHMP reviews drug applications for all 27 countries in the European Union1 as well as Iceland and Norway. The CHMP recommendation will now be considered by 1 Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, -
Annual Report 2017 DISCLAIMER
350 Annual Report 2017 DISCLAIMER Publication of Merck KGaA, Darmstadt, Germany. In the United States and Canada the subsidiaries of Merck KGaA, Darmstadt, Germany, operate as EMD Serono in Healthcare, MilliporeSigma in Life Science and EMD Performance Materials. To reflect such fact and to avoid any misconception of the reader of the publication certain logos, terms and names of businesses of the publication have been substituted or additional descriptions have been added. This version of the publication, therefore, slightly deviates from the otherwise identical version of the publication provided outside the United States and Canada. 1668 Excerpt from the “Pharmacy Privilege” issued by the ruling court to the company founder FRIEDRICH JACOB MERCK: “ [He shall run the pharmacy] ensuring that it is properly stocked with good, freshly prepared medicinal products at all times so as to cure ailments and prevent ill health.” 2018 STEFAN OSCHMANN Chairman of the Executive Board and CEO of Merck KGaA, Darmstadt, Germany “ Scientific curiosity has been a major driver of our success for 350 years. It has enabled us to pioneer new technologies. And now we are helping to shape the digital revolution.” THOUGHTS ON THE FUTURE SIMON CLARK Six young researchers is a PhD student in climate physics at the University of Exeter. His YouTube videos also mainly address topics in physics. “ Things only improve if there are people who have crazy ideas and try out something new.” Do we drive fresh ideas? Find the answer on page 10. SAMUEL CUNHA is a Brazilian parasitologist who shares his passion for biology with numerous followers on YouTube. -
Geschäftsbericht 2017
350 Geschäftsbericht 2017 1668 Auszug aus dem „Apotheken-Privileg“ des Landesherren für den Unternehmensgründer FRIEDRICH JACOB MERCK: „ [Er soll die Apotheke] der ordnung gemeess mit guten frischen, zu ein= und anderen Curen dienlichen heil- samen Medicamentis und wahren also genugsamlich versehen, und damit fort und fort würklich continuiren, daß kein Mangel erscheine.“ 2018 STEFAN OSCHMANN Vorsitzender der Geschäftsleitung und CEO von Merck „ Wissenschaftliche Neu- gierde treibt uns seit 350 Jahren an. Durch sie wurden wir Techno logie- Pioniere. Und jetzt gestalten wir die digi tale Revolution mit.“ DIE ZUKUNFT SPRICHT SIMON CLARK sechs Jungforscherinnen und -forscher promoviert im Bereich Atmosphä- rische Physik an der University of Exeter. Auch in seinen YouTube- Videos geht es vor allem um physi- kalische Themen. „ Die Dinge verbessern sich nur, wenn es Leute gibt, die ver- rückte Ideen haben und etwas Neues ausprobieren.“ Treibt Merck frische Ideen voran? Die Antwort finden Sie auf Seite 10. SAMUEL CUNHA ist ein brasilianischer Parasitologe, der seine Leidenschaft für Biologie mit vielen Fans auf YouTube teilt. „ Um leidenschaftlich zu bleiben, muss man immer an die Zukunft denken, an das mögliche Ergebnis seiner Arbeit.“ Wie hält es Merck mit diesem Grundsatz? Die Antwort lesen Sie auf Seite 11. EVA AMSEN ist promovierte Biochemikerin, Autorin und Wissenschaftsvermittlerin in London. „ Für Wissen- schaftler ist es wichtig, dass sie sich nicht nur mit ihren Kollegen austauschen, sondern auch mit Menschen aus völlig anderen Bereichen – zum Bei- spiel mit Künstlern.“ Wird interdisziplinärer Austausch bei Merck gelebt? Die Antwort lesen Sie auf Seite 13. INÉS DAWSON ist promovierte Biologin in Oxford und beliebte YouTuberin. „ Forschung und Kreativität sollten Hand in Hand gehen, da nicht alle Probleme eine eindeutige Lösung haben.“ Fördert Merck Kreativität? Die Antwort finden Sie auf Seite 14. -
Serono and Amgen Sign License Agreement for Multiple Sclerosis Product
Serono And Amgen Sign License Agreement For Multiple Sclerosis Product November 13, 2002 FOR IMMEDIATE RELEASE THOUSAND OAKS, California, USA and GENEVA, SWITZERLAND - November 13, 2002 - Amgen Inc. (NASDAQ:AMGN) and Serono S.A. (virt-x: SEO and NYSE: SRA). Amgen and Serono announced today that they have signed a license and commercialization agreement by which Serono will sell the marketed drug Novantrone® (mitoxantrone for injection concentrate) in the United States. Novantrone is approved by the FDA in the United States for secondary progressive, progressive relapsing and worsening relapsing-remitting multiple sclerosis, as well as for certain forms of cancer in the United States. The terms were undisclosed. Novantrone was acquired by Amgen in connection with Amgen's acquisition of Immunex Corporation in July 2002. The drug was approved by the FDA for MS indications in October, 2000, and had U.S. sales of $71 million last year. It has also been approved for certain oncology indications since 1987. Full prescribing information for Novantrone can be obtained by visiting www.novantrone.com. Closing of the transaction is subject to review and clearance by U.S. regulatory authorities. Amgen is a global biotechnology company that discovers, develops, manufactures and markets important human therapeutics based on advances in cellular and molecular biology. Serono is a global biotechnology leader with six recombinant products on the market, Gonal-F®, Luveris®, Ovidrel®/Ovitrelle®, Rebif®, Serostim® and Saizen® (somatropin). (Luveris® is not approved in the USA). This news release contains forward-looking statements that involve significant risks and uncertainties, including the possibility that the license transaction will not close or that the companies may be required to modify aspects of the transaction to achieve regulatory approval, and other risks and uncertainties including those discussed below and more fully described in the Securities and Exchange Commission reports filed by Amgen, including its most recent Form 10-Q. -
Merck Annual Report 2009
More information inside the cover: Business development 2000 – 2009 Merck CONTENTS Annual Report 2009 Publication contributors Published on February 23, 2010 by Merck KGaA, Corporate Communications Frankfurter Strasse 250, 64293 Darmstadt, Germany Tel.: +49 (0) 6151-72 0, fax: +49 (0) 6151-72 5577 E-mail: [email protected] Website: www.merck.de Concept, design and typesetting: XEO GmbH, Düsseldorf, Germany Annual Report 2009 Photographs: Pages 6, 10 and 11: Catrin Moritz, Essen; Pages 1, 2, 4, 35, 51, 57, and 63: Reinhard Koslowski, Düsseldorf Printing: Franz Kuthal GmbH & Co. KG, Mainaschaff, Germany Paper: FSC-certified “heaven 42” by Scheufelen W 840 539 350210 www.merck.de Contents Contents COMPANY BUSINESS DEVELOPMENT 2000 – 2009 2 The history of Merck This overview may include historically adjusted values in order to ensure comparability with 2009. 3 Becoming a global, publicly listed company 4 Merck today 4 The future Change vs. 2008 € million 2000 2001 2002 2003 2004 2005 20061 20071 2008 2009 in % Total revenues 2 6,910 7,721 7,521 7,364 6,017 5,887 4,485 7,081 7,590 7,747 2.1 TO OUR SHAREHOLDERS Pharmaceuticals 3,047 3,484 3,265 3,458 3,601 3,905 2,338 4,900 5,456 5,812 6.5 6 Letter from Karl-Ludwig Kley Merck Serono 1,941 2,228 1,850 1,546 1,619 1,817 1,938 4,480 5,014 5,345 6.6 10 Executive Board Generics 3 790 936 1,096 1,585 1,625 1,712 – – – – – Consumer Health Care 299 320 319 327 357 376 400 420 442 467 5.7 3 MANAGEMENT REPORT Imaging 17 – – – – – – – – – – Chemicals 1,679 1,729 1,791 1,707 1,696 1,906 2,113 2,152 2,127 -
Rationale and Design of Classic-MS Study
Rationale and Design of Classic-MS METHODS Study Evaluating Long-Term Efficacy for • Following pre-baseline screening and assessment for eligibility, long-term Table 2. CLASSIC-MS Schedule of Data Collection Patients with Multiple Sclerosis Treated retrospective data will be obtained from medical records at Study Visit 1; prospective data will be collected at Study Visits 1 and 2. Assessments & Procedures Screening Study Visit 1* Study Visit 2† with Cladribine Tablets • Patients will be enrolled during 17 months between Q3 2019–Q4 2020. Informed consent X • The last Patient Last Visit is expected in Q1 2021. 1 2 3 4 5 6,7 8 9 A. Boyko , J. Correale , G. Edan , M.S. Freedman , G. Giovannoni , X. Montalban , K. Rammohan , T. Leist , Inclusion and exclusion 10 11 12 13 12 GET POSTER PDF X D. Stefoski ,B. Yamout , B. Garcia-Alonso , A. Aydemir , E. Verdun Di Cantogno , on behalf of the CLASSIC-MS Copies of this poster obtained criteria Study Group through QR (Quick Response) code Figure 1. CLASSIC-MS Study Visit and Data Collection Sociodemographic and are for personal use only and may X clinical characteristics 1Pirogov Russian National Research Medical University, Moscow, Russia; 2FLENI Institute, Buenos Aires, Argentina; 3Department of not be reproduced without written 4 permission of the authors Neurology, University Hospital of Rennes, France; University of Ottawa and the Ottawa Hospital Research Institute, Ottawa, ON, Key: Prospective Data Collection Canada; 5Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK; 6Division of Neurology, St Michael’s Hospital, University of Toronto, Toronto, ON, Canada; 7Department of Neurology-Neuroimmunology, Prospective data collected atas StudyStudy VisiVisitt Physical examination X 8 Centre d’Esclerosi Múltiple de Catalunya (Cemcat), Hospital Universitario Vall d’Hebron, Barcelona, Spain; University of Miami School Retrospective data obtained from medical chart review and/or in-house study databases.