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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Amgen</span></h1>
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<div id="mw-content-text" class="mw-body-content mw-content-ltr" lang="de" dir="ltr"><div class="mw-content-ltr mw-parser-output" lang="de" dir="ltr"><table class="toccolours infobox float-right toptextcells vorlage-infobox-unternehmen" style="font-size:90%; max-width:25em; margin-top:0;" summary="Infobox Unternehmen">

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<th colspan="2" class="hintergrundfarbe5" style="font-size:110%;">Amgen Inc.
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<td colspan="2" class="notheme" style="background:#f8f9fa; color:#202122; padding:1em 0;">
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<td style="font-weight:bold;"><a href="Rechtsform" title="Rechtsform">Rechtsform</a>
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<td><a href="Gesellschaftsrecht_der_Vereinigten_Staaten#Corporation" title="Gesellschaftsrecht der Vereinigten Staaten">Incorporated</a>
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<td style="font-weight:bold;"><a href="Internationale_Wertpapierkennnummer" title="Internationale Wertpapierkennnummer">ISIN</a>
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<td><a class="external text" href="https://iw.toolforge.org/isin?language=de&amp;isin=US0311621009">US0311621009</a>
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<td style="font-weight:bold;"><a href="Gr%C3%BCndung_(Recht)" title="Gründung (Recht)">Gründung</a>
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<td><a href="1980" title="1980">1980</a>
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<td style="font-weight:bold;"><a href="Sitz_(juristische_Person)" title="Sitz (juristische Person)">Sitz</a>
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<td><a href="Thousand_Oaks" title="Thousand Oaks">Thousand Oaks</a>, <span style="display:none">Vereinigte Staaten</span><span class="mw-image-border noviewer" typeof="mw:File"><a href="Vereinigte_Staaten" title="Vereinigte Staaten"></a></span>&nbsp;<a href="Vereinigte_Staaten" title="Vereinigte Staaten">Vereinigte Staaten</a>
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<td style="font-weight:bold;"><a href="Unternehmensf%C3%BChrung" title="Unternehmensführung">Leitung</a>
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<td>Robert Bradway (<a href="Chair_of_the_Board" title="Chair of the Board">Chairman</a>, <a href="Corporate_President" title="Corporate President">President</a> und <a href="Chief_Executive_Officer" title="Chief Executive Officer">CEO</a>)<sup id="cite_ref-factsheet_1-0" class="reference"><a href="#cite_note-factsheet-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-2012CEO_2-0" class="reference"><a href="#cite_note-2012CEO-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup>
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<td style="font-weight:bold;"><a href="Mitarbeiter" title="Mitarbeiter">Mitarbeiterzahl</a>
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<td>ca. 27.000 (2025)<sup id="cite_ref-factsheet_1-1" class="reference"><a href="#cite_note-factsheet-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>
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<td style="font-weight:bold;"><a href="Erl%C3%B6s" title="Erlös">Umsatz</a>
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<td>33,4 Mrd. US-Dollar (2024)<sup id="cite_ref-2024_financials_3-0" class="reference"><a href="#cite_note-2024_financials-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
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<td style="font-weight:bold;"><a href="Wirtschaftszweig" title="Wirtschaftszweig">Branche</a>
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<td><a href="Biotechnologie" title="Biotechnologie">Biotechnologie</a>
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<td style="font-weight:bold;">Website
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<td><a rel="nofollow" class="external text" href="http://www.amgen.com/">www.amgen.com</a><br> <a rel="nofollow" class="external text" href="http://www.amgen.de/">www.amgen.de</a>
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<p>Das Biotechnologieunternehmen <b>Amgen</b> wurde 1980 als <b>AMGen</b> (<b>Applied Molecular Genetics</b>) gegründet. Amgen ist mit ca. 20.000 Mitarbeitern eines der weltweit größten <a href="Biotechnologie" title="Biotechnologie">Biotechnologieunternehmen</a> mit einem Jahresumsatz 2024 von 33,4 Milliarden US-Dollar.<sup id="cite_ref-2024_financials_3-1" class="reference"><a href="#cite_note-2024_financials-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup> Seit 1983 ist Amgen unter dem Symbol AMGN an der US-amerikanischen Technologiebörse <a href="Nasdaq" title="Nasdaq">Nasdaq</a> gelistet. Neben dem Hauptsitz in <a href="Thousand_Oaks" title="Thousand Oaks">Thousand Oaks</a> (<a href="Kalifornien" title="Kalifornien">Kalifornien</a>) und diversen Niederlassungen in den USA (unter anderem in <a href="Seattle" title="Seattle">Seattle</a> (<a href="Washington_(Bundesstaat)" title="Washington (Bundesstaat)">Washington</a>), <a href="San_Francisco" title="San Francisco">San Francisco</a> (Kalifornien) und <a href="Cambridge_(Massachusetts)" title="Cambridge (Massachusetts)">Cambridge (Massachusetts)</a>) hat das Unternehmen Niederlassungen in Kanada, Europa (unter anderem Österreich, Frankreich, Deutschland, Belgien, Italien und England) sowie in Australien, Neuseeland und Japan. Die Europazentrale befindet sich im schweizerischen <a href="Rotkreuz_ZG" title="Rotkreuz ZG">Rotkreuz</a>. Für die osteuropäischen Länder ist die Zentrale in <a href="Wien" title="Wien">Wien</a> verantwortlich.
</p><p>Hauptwachstumspräparate sind: <i>Blincyto</i> (<a href="Blinatumomab" title="Blinatumomab">Blinatumomab</a>), <i>Evenity</i> (<a href="Romosozumab" title="Romosozumab">Romosozumab</a>), <i>Repatha</i> (<a href="Evolocumab" title="Evolocumab">Evolocumab</a>), <i>Tavneos</i> (<a href="Avacopan" title="Avacopan">Avacopan</a>) und <i>Tezspire</i> (<a href="Tezepelumab" title="Tezepelumab">Tezepelumab</a>).<sup id="cite_ref-2024_financials_3-2" class="reference"><a href="#cite_note-2024_financials-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup>
</p>

<div class="mw-heading mw-heading2"><h2 id="Biotechnologie">Biotechnologie</h2></div>
<p>Der Erfolg des Unternehmens gründet sich auf der Anwendung der <a href="Rekombinante_DNA" title="Rekombinante DNA">rekombinanten DNA</a>-Technologie oder auch <a href="Rote_Biotechnologie" title="Rote Biotechnologie">Biotechnologie</a> genannt. Diese ermöglicht es, humane <a href="Protein" title="Protein">Proteine</a>, z.&nbsp;B. <a href="Hormone" class="mw-redirect" title="Hormone">Hormone</a> oder <a href="Monoklonale_Antik%C3%B6rper" class="mw-redirect" title="Monoklonale Antikörper">Monoklonale Antikörper</a> mithilfe von <a href="Mikroorganismus" title="Mikroorganismus">Mikroorganismen</a> zu produzieren. Dieser Technologie bedienen sich auch andere große Biotechnologieunternehmen, wie zum Beispiel <a href="Abbvie" title="Abbvie">Abbvie</a>, <a href="Biogen_(Unternehmen)" title="Biogen (Unternehmen)">Biogen</a>, <a href="Genentech" title="Genentech">Genentech</a>, <a href="Genzyme" title="Genzyme">Genzyme</a>, <a href="MSD_Sharp_%26_Dohme" class="mw-redirect" title="MSD Sharp &amp; Dohme">MSD</a>, <a href="Hoffmann-La_Roche" class="mw-redirect" title="Hoffmann-La Roche">Roche</a> und <a href="Sanofi" title="Sanofi">Sanofi</a>.
</p>
<div class="mw-heading mw-heading2"><h2 id="Medikamente">Medikamente</h2></div>
<p>Das Unternehmen führte zwei der ersten in Mikroorganismen produzierten humanen <a href="Therapeutikum" class="mw-redirect" title="Therapeutikum">Therapeutika</a>, so genannte <a href="Biologicals" class="mw-redirect" title="Biologicals">Biologicals</a> zur Marktreife: 1989 wurde <i>Epogen</i> (Epoetin alfa) und 1991 <i>Neupogen</i> (Filgrastim) von der <a href="Food_and_Drug_Administration" title="Food and Drug Administration">amerikanischen Zulassungsbehörde</a> (englisch <i>Food and Drug Administration</i>, FDA) zugelassen. Diese beiden Medikamente entwickelten sich zu den ersten <a href="Blockbuster_(Pharmazie)" title="Blockbuster (Pharmazie)">Blockbustern</a> der Biotechnologieindustrie.
</p><p><i>Epogen</i> beinhaltet als Wirkstoff das <a href="Hormon" title="Hormon">Hormon</a> <a href="Erythropoetin" title="Erythropoetin">Erythropoetin</a> alpha, welches normalerweise in interstitiellen Zellen der Tubuli bei Abfall des <a href="Sauerstoffpartialdruck" class="mw-redirect" title="Sauerstoffpartialdruck">Sauerstoffpartialdrucks</a> in der <a href="Nierenrinde" class="mw-redirect" title="Nierenrinde">Nierenrinde</a> gebildet wird und die Produktion neuer <a href="Erythrozyt" title="Erythrozyt">Erythrozyten</a> im <a href="Knochenmark" title="Knochenmark">Knochenmark</a> fördert. Epogen wird deshalb zur Behandlung von Blutarmut (<a href="An%C3%A4mie" title="Anämie">Anämie</a>) in Zusammenhang mit chronischen Fehlfunktionen der Nieren bei <a href="Dialyse" title="Dialyse">Dialysepatienten</a> verschrieben. Weiterhin wird es – missbräuchlich – als <a href="Dopingmittel" class="mw-redirect" title="Dopingmittel">Dopingmittel</a> im Sport eingesetzt.
</p><p><i>Neupogen</i> (<a href="G-CSF" title="G-CSF">G-CSF</a> oder auch <a href="Filgrastim" class="mw-redirect" title="Filgrastim">Filgrastim</a>) und das im Jahr 2002 zugelassene <i>Neulasta</i> (<a href="Pegfilgrastim" title="Pegfilgrastim">Pegfilgrastim</a>, also <a href="PEGylierung" title="PEGylierung">pegyliertes</a> Filgrastim) werden unter anderem angewendet, um <a href="Infektion" title="Infektion">Infektionen</a> im Verlauf einer <a href="Chemotherapie" title="Chemotherapie">Chemotherapie</a>-induzierten <a href="Neutropenie" title="Neutropenie">Neutropenie</a> entgegenzuwirken.
</p><p>Bei dem 1998 zugelassenen <i>Enbrel</i> (<a href="Etanercept" title="Etanercept">Etanercept</a>) handelt es sich um einen TNF (<i><a href="Tumornekrosefaktor" title="Tumornekrosefaktor">Tumor Necrosis Factor</a></i>)-<a href="Antagonist_(Pharmakologie)" title="Antagonist (Pharmakologie)">Antagonisten</a>, der zur Behandlung von entzündlichen Prozessen eingesetzt wird, die z.&nbsp;B. im Zusammenhang mit <a href="Rheumatoide_Arthritis" title="Rheumatoide Arthritis">rheumatoider Arthritis</a> oder der Schuppenflechte (<a href="Psoriasis" class="mw-redirect" title="Psoriasis">Psoriasis</a>) auftreten. In Deutschland wird Enbrel von ehemals <a href="Wyeth" title="Wyeth">Wyeth</a> vertrieben, einem Unternehmen, das 2009 von <a href="Pfizer" title="Pfizer">Pfizer</a> gekauft wurde.<sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup>
</p><p>Im Jahr 2001 wurde <i>Aranesp</i> (<a href="Erythropoetin#Modifikationen_des_EPO-Moleküls" title="Erythropoetin">Darbepoetin alpha</a>) zur Behandlung der <a href="Blutarmut" class="mw-redirect" title="Blutarmut">Blutarmut</a> bei chronischem Nierenversagen und nach Chemotherapie zugelassen. Im gleichen Jahr kam mit <i>Kineret</i> (Anakinra), das erste Medikament aus Reihe der <a href="Rheumatoide_Arthritis" title="Rheumatoide Arthritis">antirheumatischen</a> Medikamente von Amgen auf den Markt. (<i>Enbrel</i> kam durch den Zukauf der Immunex Corporation ins Amgen Portfolio.)
</p><p>Ein weiteres von Amgen entwickeltes Medikament ist der humane Keratinozyten-<a href="Wachstumsfaktor_(Protein)" title="Wachstumsfaktor (Protein)">Wachstumsfaktor</a> (KGF) <i>Kepivance</i> (Palifermin), der zur Behandlung von Patienten mit oraler <a href="Mukositis" title="Mukositis">Mukositis</a>, also einer Entzündung der Mundschleimhaut, die als Nebenwirkung von Chemotherapien auftreten können, zur Anwendung kommt.
</p><p>2004 wurde <i>Sensipar</i> (<a href="Cinacalcet" title="Cinacalcet">Cinacalcet</a>) von der FDA zugelassen. In der <a href="EU" class="mw-redirect" title="EU">EU</a> unter dem Namen <i>Mimpara</i> ebenfalls seit 2004 zugelassen, verringert das Medikament die Freisetzung von <a href="Parathormon" title="Parathormon">Parathormon</a> aus den Nebenschilddrüsen und wird zur Behandlung des sekundären <a href="Hyperparathyreoidismus" title="Hyperparathyreoidismus">Hyperparathyreoidismus</a> bei Patienten mit chronischen Nierenkrankheiten und erhöhten <a href="Kalzium" class="mw-redirect" title="Kalzium">Kalziumwerten</a> im Blut (<a href="Hyperkalz%C3%A4mie" title="Hyperkalzämie">Hyperkalzämie</a>) bei Patienten mit <a href="Tumor" title="Tumor">Tumoren</a> der <a href="Nebenschilddr%C3%BCse" title="Nebenschilddrüse">Nebenschilddrüse</a> (Parathyroidea) eingesetzt.
</p><p>2009 wurden <i>Nplate</i> (<a href="Romiplostim" title="Romiplostim">Romiplostim</a>) zur Behandlung der <a href="Idiopathische_thrombozytopenische_Purpura" title="Idiopathische thrombozytopenische Purpura">idiopathischen thrombozytopenischen Purpura</a> (ITP), auch Morbus Werlhof genannt, und <i>Vectibix</i> (<a href="Panitumumab" title="Panitumumab">Panitumumab</a>) zur Behandlung von <a href="Darmkrebs" class="mw-redirect" title="Darmkrebs">Darmkrebs</a> zugelassen.
</p><p><i>Prolia</i> (<a href="Denosumab" title="Denosumab">Denosumab</a>) wurde im Mai 2010 in der EU zur Behandlung der <a href="Osteoporose" title="Osteoporose">Osteoporose</a> zugelassen.<sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup> Kurz darauf hat die US-amerikanische Zulassungsbehörde <a href="Food_and_Drug_Administration" title="Food and Drug Administration">Food and Drug Administration</a> (FDA) Denosumab für die USA in dieser Indikation zugelassen.<sup id="cite_ref-6" class="reference"><a href="#cite_note-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup>
</p><p>Die <a href="Food_and_Drug_Administration" title="Food and Drug Administration">FDA</a> hatte im November 2010 Denosumab (Handelsname: <i>XGEVA</i>) für die USA zur Prävention skelettbezogener Komplikationen bei Patienten mit <a href="Knochenmetastase" title="Knochenmetastase">Knochenmetastasen</a> durch solide Tumoren zugelassen,<sup id="cite_ref-7" class="reference"><a href="#cite_note-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup> im Juli 2011 folgte die Zulassung durch die Europäische Kommission für den EU-Markt.<sup id="cite_ref-8" class="reference"><a href="#cite_note-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup> Im Juni 2013 erhielt Amgen von der FDA für <i>XGEVA</i> die Zulassung für die USA zur Behandlung von <a href="Riesenzelltumor" title="Riesenzelltumor">Riesenzelltumoren</a> des Knochens. Denosumab ist das erste FDA zugelassene Medikament für diese <a href="Seltene_Krankheit" title="Seltene Krankheit">seltene Erkrankung</a>.<sup id="cite_ref-9" class="reference"><a href="#cite_note-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup>
</p><p><i>Repatha</i> (<a href="Evolocumab" title="Evolocumab">Evolocumab</a>) wurde in der EU im Juli 2015 zur Behandlung der <a href="Homozygote_famili%C3%A4re_Hypercholesterin%C3%A4mie" title="Homozygote familiäre Hypercholesterinämie">familiären Hypercholesterinämie</a> (<a href="Cholesterin" title="Cholesterin">erhöhter Cholesterinspiegel</a>) zugelassen. Der <a href="Monoklonaler_Antik%C3%B6rper" title="Monoklonaler Antikörper">monoklonale Antikörper</a> (ein <a href="PCSK9" title="PCSK9">PCSK9</a>-Antikörper) greift in den <a href="Cholesterin" title="Cholesterin">Cholesterinstoffwechsel</a> ein und übt Einfluss auf das <a href="LDL-Cholesterin" class="mw-redirect" title="LDL-Cholesterin">LDL-Cholesterin</a> aus.<sup id="cite_ref-10" class="reference"><a href="#cite_note-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-11" class="reference"><a href="#cite_note-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup> <i>Repatha</i> ist ebenfalls zugelassen, wenn <a href="Statin" title="Statin">Statine</a> nicht vertragen werden oder diese nicht ausreichen. Er kann auch mit Statinen oder anderen <a href="Lipidsenker" title="Lipidsenker">Lipidsenkern</a> kombiniert werden.<sup id="cite_ref-12" class="reference"><a href="#cite_note-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup>
</p><p><i>Kyprolis</i> (<a href="Carfilzomib" title="Carfilzomib">Carfilzomib</a>) wurde in der EU im November 2015 zur Behandlung des <a href="Multiples_Myelom" title="Multiples Myelom">Multiplen Myeloms</a> in Kombination mit <a href="Lenalidomid" title="Lenalidomid">Lenalidomid</a> und <a href="Dexamethason" title="Dexamethason">Dexamethason</a> zugelassen.<sup id="cite_ref-13" class="reference"><a href="#cite_note-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-PMAMG25092015-ENG_14-0" class="reference"><a href="#cite_note-PMAMG25092015-ENG-14"><span class="cite-bracket">[</span>14<span class="cite-bracket">]</span></a></sup> Die Zulassung in den USA war bereits im Juli 2015 erfolgt.<sup id="cite_ref-15" class="reference"><a href="#cite_note-15"><span class="cite-bracket">[</span>15<span class="cite-bracket">]</span></a></sup>
</p><p><i>Blincyto</i> (<a href="Blinatumomab" title="Blinatumomab">Blinatumomab</a>) wurde im November 2015 in der EU zur Behandlung spezieller Formen der <a href="Akute_lymphatische_Leuk%C3%A4mie" title="Akute lymphatische Leukämie">akuten lymphatischen Leukämie (ALL)</a> zugelassen.<sup id="cite_ref-PM-Amgen-2116999_16-0" class="reference"><a href="#cite_note-PM-Amgen-2116999-16"><span class="cite-bracket">[</span>16<span class="cite-bracket">]</span></a></sup> Die Zulassung in den USA war bereits im Dezember 2014 erfolgt.<sup id="cite_ref-PM-FDA-425597_17-0" class="reference"><a href="#cite_note-PM-FDA-425597-17"><span class="cite-bracket">[</span>17<span class="cite-bracket">]</span></a></sup> Von der US-amerikanischen Zulassungsbehörde FDA erhielt Blinatumomab die <a href="FDA_Expedited_Program#Breakthrough_Therapy" title="FDA Expedited Program">Breakthrough Therapy Designation</a> (englisch für „Durchbruch in der Therapie“) und wurde sowohl in den USA als auch in der EU als <i><a href="Orphan_Drug" class="mw-redirect" title="Orphan Drug">Orphan Drug</a></i> (Arzneimittel für seltene Leiden) ausgewiesen.<sup id="cite_ref-PM-Amgen-2116999_16-1" class="reference"><a href="#cite_note-PM-Amgen-2116999-16"><span class="cite-bracket">[</span>16<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-PM-FDA-425597_17-1" class="reference"><a href="#cite_note-PM-FDA-425597-17"><span class="cite-bracket">[</span>17<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-18" class="reference"><a href="#cite_note-18"><span class="cite-bracket">[</span>18<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-19" class="reference"><a href="#cite_note-19"><span class="cite-bracket">[</span>19<span class="cite-bracket">]</span></a></sup>
</p><p><i>Imlygic</i> (<a href="Talimogen_laherparepvec" title="Talimogen laherparepvec">Talimogen laherparepvec</a> / T-VEC / früher Onco<sup>VEX GM-CSF</sup>) wurde im Dezember 2015 von der Europäischen Kommission für die Länder der EU zur Behandlung des <a href="Malignes_Melanom" title="Malignes Melanom">Malignen Melanoms</a> (Hautkrebs) zugelassen.<sup id="cite_ref-EU-Zulassung_T-Vec_20-0" class="reference"><a href="#cite_note-EU-Zulassung_T-Vec-20"><span class="cite-bracket">[</span>20<span class="cite-bracket">]</span></a></sup> Es handelt sich dabei um das erste zugelassene <a href="Onkolytische_Viren" title="Onkolytische Viren">onkolytisch wirkende Immuntherapeutikum</a>.<sup id="cite_ref-CHMP_T-Vec_21-0" class="reference"><a href="#cite_note-CHMP_T-Vec-21"><span class="cite-bracket">[</span>21<span class="cite-bracket">]</span></a></sup> Die Zulassung in den USA war bereits im Oktober 2015 erfolgt.<sup id="cite_ref-22" class="reference"><a href="#cite_note-22"><span class="cite-bracket">[</span>22<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-melanoma_23-0" class="reference"><a href="#cite_note-melanoma-23"><span class="cite-bracket">[</span>23<span class="cite-bracket">]</span></a></sup>
</p><p><i>Parsabiv</i> (<a href="Etelcalcetid" title="Etelcalcetid">Etelcalcetid</a>) wurde im November 2016 von der Europäischen Kommission für die Länder der EU zur Senkung der <a href="Parathormon" title="Parathormon">Parathormon</a>-Spiegel bei Erwachsenen mit hohen Spiegeln dieses Hormons aufgrund einer langfristigen Nierenerkrankung (<a href="Hyperparathyreoidismus" title="Hyperparathyreoidismus">sekundärer Hyperparathyreoidismus</a>) zugelassen.<sup id="cite_ref-24" class="reference"><a href="#cite_note-24"><span class="cite-bracket">[</span>24<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-25" class="reference"><a href="#cite_note-25"><span class="cite-bracket">[</span>25<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-26" class="reference"><a href="#cite_note-26"><span class="cite-bracket">[</span>26<span class="cite-bracket">]</span></a></sup>
</p><p><i>Amgevita</i> (<a href="Biosimilar" title="Biosimilar">Biosimilar</a> <a href="Adalimumab" title="Adalimumab">Adalimumab</a>) wurde im März 2017 von der Europäischen Kommission für die Länder der EU zur Behandlung von verschiedenen entzündlichen Erkrankungen (<a href="Rheumatoide_Arthritis" title="Rheumatoide Arthritis">Rheumatoide Arthritis</a>, <a href="Psoriasis-Arthritis" class="mw-redirect" title="Psoriasis-Arthritis">Psoriasis-Arthritis</a>, <a href="Spondylitis_ankylosans" title="Spondylitis ankylosans">Spondylitis ankylosans</a>, Chronisch-entzündliche Darmerkrankungen (<a href="Morbus_Crohn" title="Morbus Crohn">Morbus Crohn</a>) und <a href="Colitis_ulcerosa" title="Colitis ulcerosa">Colitis ulcerosa</a>) zugelassen.<sup id="cite_ref-amgevita_27-0" class="reference"><a href="#cite_note-amgevita-27"><span class="cite-bracket">[</span>27<span class="cite-bracket">]</span></a></sup>
</p><p><i>Aimovig</i> (<a href="Erenumab" title="Erenumab">Erenumab-aooe</a>), ist ein von Amgen und <a href="Novartis" title="Novartis">Novartis</a> gemeinsam entwickelter humaner monoklonaler Antikörper, der im Mai 2018 in den USA zur <a href="Pr%C3%A4vention" title="Prävention">Prävention</a> von <a href="Migr%C3%A4ne" title="Migräne">Migräne</a> zugelassen wurde.<sup id="cite_ref-28" class="reference"><a href="#cite_note-28"><span class="cite-bracket">[</span>28<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-29" class="reference"><a href="#cite_note-29"><span class="cite-bracket">[</span>29<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-30" class="reference"><a href="#cite_note-30"><span class="cite-bracket">[</span>30<span class="cite-bracket">]</span></a></sup> Die europäische Zulassung erfolgte im August 2018.<sup id="cite_ref-31" class="reference"><a href="#cite_note-31"><span class="cite-bracket">[</span>31<span class="cite-bracket">]</span></a></sup> In Europa wird <i>Aimovig</i> von Novartis vertrieben.<sup id="cite_ref-32" class="reference"><a href="#cite_note-32"><span class="cite-bracket">[</span>32<span class="cite-bracket">]</span></a></sup>
</p><p><i>Evenity</i> (<a href="Romosozumab" title="Romosozumab">Romosozumab</a>) ist ein monoklonaler Antikörper, der im April 2019 in den USA zur Prävention von <a href="Osteoporose" title="Osteoporose">Osteoporose</a> zugelassen wurde.<sup id="cite_ref-FDA_Romosozumab_33-0" class="reference"><a href="#cite_note-FDA_Romosozumab-33"><span class="cite-bracket">[</span>33<span class="cite-bracket">]</span></a></sup> Das CHMP der EMA sprach sich im Oktober 2019 für eine Zulassung in der EU aus.<sup id="cite_ref-pipeline_34-0" class="reference"><a href="#cite_note-pipeline-34"><span class="cite-bracket">[</span>34<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-35" class="reference"><a href="#cite_note-35"><span class="cite-bracket">[</span>35<span class="cite-bracket">]</span></a></sup> Im Dezember 2019 erteilte die EMA dem Wirkstoff die Zulassung für die Anwendung bei Frauen nach der <a href="Menopause" title="Menopause">Menopause</a> zur Behandlung der manifesten Osteoporose, wenn ein deutlich erhöhtes Risiko für Knochenbrüche besteht.<sup id="cite_ref-iqwig.de_36-0" class="reference"><a href="#cite_note-iqwig.de-36"><span class="cite-bracket">[</span>36<span class="cite-bracket">]</span></a></sup> (s.&nbsp;a. Kooperationen)
</p><p><i>Otezla</i> (<a href="Apremilast" title="Apremilast">Apremilast</a>) wurde in den Jahren 2019 / 2020 von <a href="Celgene" title="Celgene">Celgene</a> übernommen. Der orale niedermolekulare Phosphodiesterase 4 (PDE4)-Inhibitor wird zur Behandlung von <a href="Psoriasis" class="mw-redirect" title="Psoriasis">Psoriasis</a> eingesetzt. Celgene selbst wurde in den Jahren 2019–2021 an <a href="Bristol-Myers_Squibb" title="Bristol-Myers Squibb">BMS</a> verkauft.<sup id="cite_ref-37" class="reference"><a href="#cite_note-37"><span class="cite-bracket">[</span>37<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-38" class="reference"><a href="#cite_note-38"><span class="cite-bracket">[</span>38<span class="cite-bracket">]</span></a></sup>
</p><p><i>Lumykras</i> (<a href="Sotorasib" title="Sotorasib">Sotorasib</a>) ist ein Arzneistoff der KRAS-Inhibitoren, der gegen <a href="Tumor" title="Tumor">Tumoren</a> mit Mutationen im K<a href="G-Protein_Ras#Krebsforschung" title="G-Protein Ras">Ras</a>-Gen eingesetzt wird. In den USA ist er seit Mai 2021 zugelassen zur Behandlung des <a href="Bronchialkarzinom#Nichtkleinzelliges_Bronchialkarzinom_(NSCLC)_–_Therapie" title="Bronchialkarzinom">nicht-kleinzelligen Lungenkrebses</a> (NSCLC).<sup id="cite_ref-FDA-20210528_39-0" class="reference"><a href="#cite_note-FDA-20210528-39"><span class="cite-bracket">[</span>39<span class="cite-bracket">]</span></a></sup> In der EU wurde Sotorasib im Januar 2022 zugelassen.<sup id="cite_ref-40" class="reference"><a href="#cite_note-40"><span class="cite-bracket">[</span>40<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Forschung_und_Entwicklung">Forschung und Entwicklung</h2></div>
<p>Als weltweit größtes Biotechnologieunternehmen hat das Unternehmen zahlreiche <a href="Monoklonaler_Antik%C3%B6rper" title="Monoklonaler Antikörper">monoklonale Antikörper</a> in der klinischen Entwicklung (Phase I-III).<sup id="cite_ref-pipeline_34-1" class="reference"><a href="#cite_note-pipeline-34"><span class="cite-bracket">[</span>34<span class="cite-bracket">]</span></a></sup> In Phase III befindliche Arzneistoffe sind z.&nbsp;B. Rilotumumab (<a href="Magenkrebs" class="mw-redirect" title="Magenkrebs">Magenkrebs</a>),<sup id="cite_ref-pipeline_34-2" class="reference"><a href="#cite_note-pipeline-34"><span class="cite-bracket">[</span>34<span class="cite-bracket">]</span></a></sup> <a href="Tezepelumab" title="Tezepelumab">Tezepelumab</a> (Asthma)<sup id="cite_ref-pipeline_34-3" class="reference"><a href="#cite_note-pipeline-34"><span class="cite-bracket">[</span>34<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-41" class="reference"><a href="#cite_note-41"><span class="cite-bracket">[</span>41<span class="cite-bracket">]</span></a></sup> und Trebananib (<a href="Ovarialkarzinom" title="Ovarialkarzinom">Eierstockkrebs</a>).<sup id="cite_ref-pipeline_34-4" class="reference"><a href="#cite_note-pipeline-34"><span class="cite-bracket">[</span>34<span class="cite-bracket">]</span></a></sup>
</p><p>Amgen widmet sich auch dem Bereich der <a href="Biosimilars" class="mw-redirect" title="Biosimilars">Biosimilars</a>. Eines der ersten Biosimilars, das Amgen in der Pipeline hat, ist ABP 501, ein Biosimilar zu <a href="Adalimumab" title="Adalimumab">Adalimumab</a> (<i>Humira</i>).<sup id="cite_ref-42" class="reference"><a href="#cite_note-42"><span class="cite-bracket">[</span>42<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-43" class="reference"><a href="#cite_note-43"><span class="cite-bracket">[</span>43<span class="cite-bracket">]</span></a></sup> In den USA ist es unter dem Handelsnamen <i>Amjevita</i> zugelassen.<sup id="cite_ref-44" class="reference"><a href="#cite_note-44"><span class="cite-bracket">[</span>44<span class="cite-bracket">]</span></a></sup> Für die EU erfolgte die Zulassungsempfehlung des <a href="Ausschuss_f%C3%BCr_Humanarzneimittel" title="Ausschuss für Humanarzneimittel">CHMP</a> für <i>Amgevita</i> im Januar 2017,<sup id="cite_ref-45" class="reference"><a href="#cite_note-45"><span class="cite-bracket">[</span>45<span class="cite-bracket">]</span></a></sup> und die Zulassung selbst im März 2017.<sup id="cite_ref-amgevita_27-1" class="reference"><a href="#cite_note-amgevita-27"><span class="cite-bracket">[</span>27<span class="cite-bracket">]</span></a></sup> Weitere Biosimilars, z.&nbsp;B. zu <a href="Bevacizumab" title="Bevacizumab">Bevacizumab</a> (<i>Avastin</i>), <a href="Cetuximab" title="Cetuximab">Cetuximab</a> (<i>Erbitux</i>), <a href="Infliximab" title="Infliximab">Infliximab</a> (<i>Remicade</i>), <a href="Trastuzumab" title="Trastuzumab">Trastuzumab</a> (<i>Herceptin</i>) und <a href="Rituximab" title="Rituximab">Rituximab</a> (<i>MabThera</i> resp. <i>Rituxan</i>) sind in der Pipeline.<sup id="cite_ref-46" class="reference"><a href="#cite_note-46"><span class="cite-bracket">[</span>46<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Akquisitionen_und_Kooperationen">Akquisitionen und Kooperationen</h2></div>
<ul><li>In 2007 gaben Amgen und Cytokinetics bekannt, dass sie gemeinsam in der Indikation „<a href="Herzinsuffizienz" title="Herzinsuffizienz">Herzinsuffizienz</a>“ forschen werden. Amgen hält die weltweiten Vermarktungsrechte eines experimentellen Wirkstoffes von Cytokinetics Omecamtiv Mecarbil (CK-1827452).<sup id="cite_ref-47" class="reference"><a href="#cite_note-47"><span class="cite-bracket">[</span>47<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-48" class="reference"><a href="#cite_note-48"><span class="cite-bracket">[</span>48<span class="cite-bracket">]</span></a></sup></li>
<li>Gemeinsam mit <a href="UCB_(Unternehmen)" title="UCB (Unternehmen)">UCB</a> startete Amgen 2011 eine Kooperation mit der NASA, um den Sclerostin-Antikörper <a href="Romosozumab" title="Romosozumab">Romosozumab</a> im Weltall in Bezug auf den Knochenschwund zu untersuchen.<sup id="cite_ref-UCB_49-0" class="reference"><a href="#cite_note-UCB-49"><span class="cite-bracket">[</span>49<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-50" class="reference"><a href="#cite_note-50"><span class="cite-bracket">[</span>50<span class="cite-bracket">]</span></a></sup> Die Kooperation mit UCB besteht bereits seit 2004. Romosozumab wurde im Januar 2019 in Japan – als erstes Land in der Welt – in der Indikation "<a href="Osteoporose" title="Osteoporose">postmenopausale Osteoporose</a>" zugelassen. Zur Vermarktung von <i>Evenity</i> besteht ein "<a href="Joint_venture" class="mw-redirect" title="Joint venture">Joint venture</a>" zwischen Amgen und <a href="Astellas_Pharma" title="Astellas Pharma">Astellas Pharma</a>: Amgen Astellas BioPharma K.K. (AABK).<sup id="cite_ref-51" class="reference"><a href="#cite_note-51"><span class="cite-bracket">[</span>51<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-52" class="reference"><a href="#cite_note-52"><span class="cite-bracket">[</span>52<span class="cite-bracket">]</span></a></sup> Im Januar 2019 erfolgte ein positives Votum für eine Zulassung in den USA durch die FDA.<sup id="cite_ref-53" class="reference"><a href="#cite_note-53"><span class="cite-bracket">[</span>53<span class="cite-bracket">]</span></a></sup> Die FDA Zulassung erfolgte im April 2019.<sup id="cite_ref-FDA_Romosozumab_33-1" class="reference"><a href="#cite_note-FDA_Romosozumab-33"><span class="cite-bracket">[</span>33<span class="cite-bracket">]</span></a></sup></li>
<li>Amgen übernahm 2012 das Biotechnologieunternehmen Micromet, welches auf die Entdeckung, Entwicklung und die Kommerzialisierung innovativer Krebstherapien auf der Basis von Antikörpern (<a href="BiTE-Antik%C3%B6rper" title="BiTE-Antikörper">BiTE-Antikörpern</a>) spezialisiert ist. Das führende Produkt von (ehemals) Micromet, <a href="Blinatumomab" title="Blinatumomab">Blinatumomab</a>, ist zwischenzeitlich sowohl in den USA als auch in der EU zugelassen.<sup id="cite_ref-PM-Amgen-2116999_16-2" class="reference"><a href="#cite_note-PM-Amgen-2116999-16"><span class="cite-bracket">[</span>16<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-PM-FDA-425597_17-2" class="reference"><a href="#cite_note-PM-FDA-425597-17"><span class="cite-bracket">[</span>17<span class="cite-bracket">]</span></a></sup></li>
<li>Amgen und <a href="AstraZeneca" title="AstraZeneca">AstraZeneca Plc</a> entwickeln und vermarkten seit 2012 gemeinsam fünf monoklonale Antikörper aus Amgens Inflammationsportfolio (AMG 139, AMG 157, AMG 181, AMG 557 und Brodalumab (AMG 827)).<sup id="cite_ref-54" class="reference"><a href="#cite_note-54"><span class="cite-bracket">[</span>54<span class="cite-bracket">]</span></a></sup> Im Mai 2015 gab Amgen bekannt, dass es die Zusammenarbeit mit AstraZeneca in Bezug auf Brodalumab beendet hat.<sup id="cite_ref-55" class="reference"><a href="#cite_note-55"><span class="cite-bracket">[</span>55<span class="cite-bracket">]</span></a></sup></li>
<li>Das Unternehmen kündigte im April 2012 an <a href="Mustafa_Nevzat_Pharmaceuticals" title="Mustafa Nevzat Pharmaceuticals">Mustafa Nevzat Pharmaceuticals</a> zu erwerben<sup id="cite_ref-56" class="reference"><a href="#cite_note-56"><span class="cite-bracket">[</span>56<span class="cite-bracket">]</span></a></sup> und kaufte Ende 2012 deCODE Genetics, ein führendes Unternehmen in der Genetik-Forschung.<sup id="cite_ref-57" class="reference"><a href="#cite_note-57"><span class="cite-bracket">[</span>57<span class="cite-bracket">]</span></a></sup></li>
<li>Ende August 2013 wurde bekannt gegeben, dass das Unternehmen <a href="Onyx_Pharmaceuticals" class="mw-redirect" title="Onyx Pharmaceuticals">Onyx Pharmaceuticals</a> für 10,4 Milliarden US-Dollar übernommen wird. Onyx besitzt die Vermarktungsrechte für <i>Kyprolis</i> (<a href="Carfilzomib" title="Carfilzomib">Carfilzomib</a> / <a href="Multiples_Myelom" title="Multiples Myelom">Multiples Myelom</a>).<sup id="cite_ref-58" class="reference"><a href="#cite_note-58"><span class="cite-bracket">[</span>58<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-59" class="reference"><a href="#cite_note-59"><span class="cite-bracket">[</span>59<span class="cite-bracket">]</span></a></sup></li>
<li>Im Februar 2014 gaben Amgen und <a href="Merck_%26_Co.%2C_Inc." class="mw-redirect" title="Merck &amp; Co., Inc.">Merck &amp; Co., Inc. (in Deutschland: MSD)</a> bekannt, dass sie gemeinsam in der Indikation „<a href="Melanom" class="mw-redirect" title="Melanom">Melanom</a>“ forschen werden. Amgen hat mit <a href="Talimogen_laherparepvec" title="Talimogen laherparepvec">Talimogen laherparepvec</a> (<i>Imlygic</i>)<sup id="cite_ref-melanoma_23-1" class="reference"><a href="#cite_note-melanoma-23"><span class="cite-bracket">[</span>23<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-EU-Zulassung_T-Vec_20-1" class="reference"><a href="#cite_note-EU-Zulassung_T-Vec-20"><span class="cite-bracket">[</span>20<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-60" class="reference"><a href="#cite_note-60"><span class="cite-bracket">[</span>60<span class="cite-bracket">]</span></a></sup> und MSD mit <a href="Pembrolizumab" title="Pembrolizumab">Pembrolizumab</a> (<i>Keytruda</i>) jeweils ein innovatives Medikament zur Melanom-Behandlung im therapeutischen Angebot.</li>
<li>Im September 2016 haben Amgen und <a href="Servier" title="Servier">Servier</a> eine Kooperations-Erweiterung im Bereich Kardio-Vaskulärer-Erkrankungen bekannt gegeben.<sup id="cite_ref-61" class="reference"><a href="#cite_note-61"><span class="cite-bracket">[</span>61<span class="cite-bracket">]</span></a></sup></li>
<li>Amgen und <a href="Novartis" title="Novartis">Novartis</a> gaben im April 2017 bekannt, dass sie gemeinsam die Produkteinführung ("Launch") des ersten ("first-in-class") Monoklonalen Antikörpers <a href="Erenumab" title="Erenumab">Erenumab</a> zur Behandlung von <a href="Migr%C3%A4ne" title="Migräne">Migräne</a> in den USA und Kanada anstreben.<sup id="cite_ref-62" class="reference"><a href="#cite_note-62"><span class="cite-bracket">[</span>62<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-63" class="reference"><a href="#cite_note-63"><span class="cite-bracket">[</span>63<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-64" class="reference"><a href="#cite_note-64"><span class="cite-bracket">[</span>64<span class="cite-bracket">]</span></a></sup></li>
<li>Bereits 2011 formierten Amgen und <a href="Allergan" title="Allergan">Allergan</a> eine Kooperation zur gemeinsamen Entwicklung von <a href="Biosimilars" class="mw-redirect" title="Biosimilars">Biosimilars</a>. Erster gemeinsamer Wirkstoff: Biosimilar zu <a href="Bevacizumab" title="Bevacizumab">Bevacizumab</a> (<i>Avastin</i>).<sup id="cite_ref-65" class="reference"><a href="#cite_note-65"><span class="cite-bracket">[</span>65<span class="cite-bracket">]</span></a></sup></li>
<li>Im Oktober 2017 gaben Amgen und CytomX Therapeutics eine strategische Kooperation in der <a href="Krebsimmuntherapie" title="Krebsimmuntherapie">Immun-Onkologie</a> bekannt.<sup id="cite_ref-66" class="reference"><a href="#cite_note-66"><span class="cite-bracket">[</span>66<span class="cite-bracket">]</span></a></sup></li>
<li>Im März 2021 erwarb Amgen das US-amerikanische, an der Nasdaq gehandelte Pharmaunternehmen Five Prime Therapeutics für 1,9 Milliarden Dollar in bar. Die Akquisition umfasst den (noch) experimentellen <a href="Monoklonaler_Antik%C3%B6rper" title="Monoklonaler Antikörper">monoklonalen Antikörper</a> Bemarituzumab, ein in <a href="Klinische_Studie" title="Klinische Studie">Phase-3</a> befindliches "<a href="First-in-class" title="First-in-class">first-in-class</a>"-Medikament zur Behandlung von <a href="Magenkrebs" class="mw-redirect" title="Magenkrebs">Magenkrebs</a>, der dritthäufigsten Todesursache bei Krebserkrankungen weltweit.<sup id="cite_ref-67" class="reference"><a href="#cite_note-67"><span class="cite-bracket">[</span>67<span class="cite-bracket">]</span></a></sup></li>
<li>Im März 2021 gaben Amgen und Rodeo Therapeutics bekannt, das Amgen Rodeo übernimmt. Rodeo ist ein privates biopharmazeutisches Unternehmen mit Sitz in <a href="Seattle" title="Seattle">Seattle</a>, das "<a href="Small_molecules" class="mw-redirect" title="Small molecules">small molecules</a>" zur Förderung der Regeneration und Reparatur von verschiedenen Geweben entwickelt. Das 15-PGDH-Programm von Rodeo sieht ebenfalls "first-in-class"-Therapeutika vor.<sup id="cite_ref-68" class="reference"><a href="#cite_note-68"><span class="cite-bracket">[</span>68<span class="cite-bracket">]</span></a></sup></li>
<li>Im Dezember 2022 wurde bekannt gegeben, dass Amgen den irisch-amerikanischen Arzneimittelhersteller <a href="Horizon_Therapeutics" class="mw-redirect" title="Horizon Therapeutics">Horizon Therapeutics</a> für 28,3 Milliarden Dollar übernehmen will: eine der größten Übernahmen in der Pharmabranche.<sup id="cite_ref-69" class="reference"><a href="#cite_note-69"><span class="cite-bracket">[</span>69<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-70" class="reference"><a href="#cite_note-70"><span class="cite-bracket">[</span>70<span class="cite-bracket">]</span></a></sup> Die <a href="Federal_Trade_Commission" title="Federal Trade Commission">Federal Trade Commission</a> (FTC) versuchte zunächst, den Zusammenschluss aus Wettbewerbsgründen zu verbieten. Im September 2023 gaben Amgen und Horizon jedoch bekannt, dass die Klage der FTC beigelegt wurde. Die Übernahme erfolgte im Oktober 2023.<sup id="cite_ref-71" class="reference"><a href="#cite_note-71"><span class="cite-bracket">[</span>71<span class="cite-bracket">]</span></a></sup> Das 23%ige Wachstum von 2024 gegenüber 2023 ist primär auf diese Akquisition zurückzuführen (ohne Horizon beträgt das Wachstum 7 Prozent gegenüber Vorjahr).<sup id="cite_ref-2024_financials_3-3" class="reference"><a href="#cite_note-2024_financials-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup></li></ul>
<div class="mw-heading mw-heading2"><h2 id="Amgen_Research_(Munich)_GmbH"><span id="Amgen_Research_.28Munich.29_GmbH"></span>Amgen Research (Munich) GmbH</h2></div>
<p>Amgen Research (Munich) GmbH, ehemals Micromet GmbH, wurde im März 2012 gegründet. Über 200 Mitarbeiter arbeiten hier in der Forschung &amp; Entwicklung, vor allem im Bereich Onkologie. Amgen Research (Munich) GmbH ist spezialisiert auf die Entwicklung von „<a href="Bispezifischer_Antik%C3%B6rper" title="Bispezifischer Antikörper">bispezifischen T-Zell Engagern</a>“ (BiTEs) für die Behandlung von Krebs. BiTE-Antikörper stimulieren die Immunzellen des Patienten zur Krebsbekämpfung.<sup id="cite_ref-72" class="reference"><a href="#cite_note-72"><span class="cite-bracket">[</span>72<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-73" class="reference"><a href="#cite_note-73"><span class="cite-bracket">[</span>73<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Galenus_von_Pergamon-Preis_(Prix_Galien)_und_Kritik"><span id="Galenus_von_Pergamon-Preis_.28Prix_Galien.29_und_Kritik"></span>Galenus von Pergamon-Preis (Prix Galien) und Kritik</h2></div>
<p>2011 erhielt das Unternehmen für zwei Medikamente den <a href="Galenus-von-Pergamon-Preis" title="Galenus-von-Pergamon-Preis">Galenus-von-Pergamon-Preis</a> (<i>Prix Galien</i>): Der monoklonale Antikörper <a href="Denosumab" title="Denosumab">Denosumab</a> (<i>Prolia</i>) ist Preisträger in der Kategorie „Primary Care“; Preisträger in der Kategorie „Specialist Care“ ist das Protein <a href="Romiplostim" title="Romiplostim">Romiplostim</a> (<i>Nplate</i>).<sup id="cite_ref-74" class="reference"><a href="#cite_note-74"><span class="cite-bracket">[</span>74<span class="cite-bracket">]</span></a></sup>
</p><p>Das Medikament <i>Prolia</i> erwies sich als wirksam gegen Knochenschwund. Allerdings steigt mit Absetzen der Medikation das Risiko von multiplen Wirbelbrüchen aufgrund eines <a href="Rebound_(Medizin)" title="Rebound (Medizin)">Reboundeffekts</a>. Die <a href="Arzneimittelkommission_der_deutschen_%C3%84rzteschaft" class="mw-redirect" title="Arzneimittelkommission der deutschen Ärzteschaft">Arzneimittelkommission der deutschen Ärzteschaft</a> empfahl daher 2018 regelmäßige <a href="Knochendichtemessung" title="Knochendichtemessung">Knochendichtemessungen</a> nach Behandlungsende.<sup id="cite_ref-75" class="reference"><a href="#cite_note-75"><span class="cite-bracket">[</span>75<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-76" class="reference"><a href="#cite_note-76"><span class="cite-bracket">[</span>76<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-77" class="reference"><a href="#cite_note-77"><span class="cite-bracket">[</span>77<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-78" class="reference"><a href="#cite_note-78"><span class="cite-bracket">[</span>78<span class="cite-bracket">]</span></a></sup>
</p>
<div class="mw-heading mw-heading2"><h2 id="Literatur">Literatur</h2></div>
<ul><li>Gordon Binder (mit Philip Bashe): <i>Science Lessons: What the Business of Biotech Taught Me About Management</i>. Harvard Business Review Press 2008<sup id="cite_ref-79" class="reference"><a href="#cite_note-79"><span class="cite-bracket">[</span>79<span class="cite-bracket">]</span></a></sup></li></ul>
<div class="mw-heading mw-heading2"><h2 id="Weblinks">Weblinks</h2></div>
<ul><li><a rel="nofollow" class="external text" href="http://www.amgen.com/">www.amgen.com</a></li>
<li><a rel="nofollow" class="external text" href="https://www.amgenbiosimilars.com/">www.amgenbiosimilars.com</a></li>
<li><a rel="nofollow" class="external text" href="http://www.amgen.de/">www.amgen.de</a></li>
<li><a rel="nofollow" class="external text" href="https://fachkreise.amgen.de/">fachkreise.amgen.de</a></li></ul>
<div class="mw-heading mw-heading2"><h2 id="Einzelnachweise">Einzelnachweise</h2></div>
<div class="mw-references-wrap mw-references-columns"><ol class="references">
<li id="cite_note-factsheet-1"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-factsheet_1-0">a</a></sup> <sup><a href="#cite_ref-factsheet_1-1">b</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/pdfs/misc/Fact_Sheet_Amgen.pdf">Amgen Fact Sheet 2022</a> Corporate Website, abgerufen am 18. Januar 2023</span>
</li>
<li id="cite_note-2012CEO-2"><span class="mw-cite-backlink"><a href="#cite_ref-2012CEO_2-0">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.amgen.com/media/media_pr_detail.jsp?year=2011&amp;releaseID=1640319">Amgen Press Release Kevin W. Sharer / Robert Bradway</a>, PM Amgen vom 15. Dezember 2011, abgerufen am 18. Januar 2023</span>
</li>
<li id="cite_note-2024_financials-3"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-2024_financials_3-0">a</a></sup> <sup><a href="#cite_ref-2024_financials_3-1">b</a></sup> <sup><a href="#cite_ref-2024_financials_3-2">c</a></sup> <sup><a href="#cite_ref-2024_financials_3-3">d</a></sup></span> <span class="reference-text"><span class="cite">Amgen: <a rel="nofollow" class="external text" href="https://www.amgen.com/stories/2025/02/highlights-from-amgens-2024-fourth-quarter-and-full-year-earnings-report"><i>Amgen Reports Fourth Quarter And Full Year 2023 Financial Results.</i></a> 4.&nbsp;Februar 2025,<span class="Abrufdatum"> abgerufen am 5.&nbsp;Februar 2025</span> (englisch).</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&amp;rfr_id=info%3Asid%2Fde.wikipedia.org%3AAmgen&amp;rft.title=Amgen+Reports+Fourth+Quarter+And+Full+Year+2023+Financial+Results&amp;rft.description=Amgen+Reports+Fourth+Quarter+And+Full+Year+2023+Financial+Results&amp;rft.identifier=&amp;rft.creator=Amgen&amp;rft.date=2025-02-04&amp;rft.language=en">&nbsp;</span></span>
</li>
<li id="cite_note-4"><span class="mw-cite-backlink"><a href="#cite_ref-4">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20111219190339/http://mediaroom.pfizer.com/portal/site/pfizer/index.jsp?ndmViewId=news_view&amp;ndmConfigId=1016273&amp;newsId=20090126005624&amp;newsLang=en">Pfizer to Acquire Wyeth, Creating the World’s Premier Biopharmaceutical Company</a>, PM Pfizer vom 26. Januar 2009, abgerufen am 18. Januar 2023</span>
</li>
<li id="cite_note-5"><span class="mw-cite-backlink"><a href="#cite_ref-5">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/media_pr_detail.jsp?releaseID=1432232"><i>Prolia(R) (Denosumab) Granted Marketing Authorization in the European Union</i>.</a> Pressemitteilung vom 28. Mai 2010</span>
</li>
<li id="cite_note-6"><span class="mw-cite-backlink"><a href="#cite_ref-6">↑</a></span> <span class="reference-text"><i><a rel="nofollow" class="external text" href="https://www.amgen.com/media/media_pr_detail.jsp?releaseID=1433162">FDA Approves Amgen’s Prolia(TM) (Denosumab) for Treatment of Postmenopausal Women With Osteoporosis at High Risk for Fracture</a></i>, Pressemitteilung vom 1. Juni 2010</span>
</li>
<li id="cite_note-7"><span class="mw-cite-backlink"><a href="#cite_ref-7">↑</a></span> <span class="reference-text"><i><a rel="nofollow" class="external text" href="http://www.amgen.com/media/media_pr_detail.jsp?year=2010&amp;releaseID=1498709">FDA Approves Amgen’s XGEVA (Denosumab) for the Prevention of Skeletal-Related Events in Patients with Bone Metastases from Solid Tumors</a></i>, Pressemitteilung vom 18. November 2010</span>
</li>
<li id="cite_note-8"><span class="mw-cite-backlink"><a href="#cite_ref-8">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/media_pr_detail.jsp?releaseID=1585714"><i>XGEVA (Denosumab) Granted Marketing Authorization in the European Union</i>.</a> Pressemitteilung vom 15. Juli 2011</span>
</li>
<li id="cite_note-9"><span class="mw-cite-backlink"><a href="#cite_ref-9">↑</a></span> <span class="reference-text"><i><a rel="nofollow" class="external text" href="https://www.amgen.com/media/media_pr_detail.jsp?releaseID=1829715">FDA Approves Amgen’s XGEVA (denosumab) For The Treatment Of Giant Cell Tumor Of Bone</a></i>, Pressemitteilung vom 13. Juni 2013</span>
</li>
<li id="cite_note-10"><span class="mw-cite-backlink"><a href="#cite_ref-10">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/media_pr_detail.jsp?releaseID=1753617"><i>Amgen To Present Data From Four Phase 2 Studies At Upcoming American Heart Association Scientific Sessions 2012</i>.</a> Pressemitteilung vom 2. November 2012</span>
</li>
<li id="cite_note-11"><span class="mw-cite-backlink"><a href="#cite_ref-11">↑</a></span> <span class="reference-text"><style data-mw-deduplicate="TemplateStyles:r261891140">
/* start https://de.wikipedia.org/ */


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</style><a rel="nofollow" class="external text" href="https://web.archive.org/web/20121213143353/http://www.amgen.com/media/amgen_aha_2012.html"><i>Amgen at AHA Scientific Sessions 2012</i>.</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 13. Dezember 2012 im <i><a href="Internet_Archive" title="Internet Archive">Internet Archive</a></i>) Übersicht anlässlich der AHA Tagung</span>
</li>
<li id="cite_note-12"><span class="mw-cite-backlink"><a href="#cite_ref-12">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://archive.today/20150722065627/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2069405">European Commission Approves Amgen’s New Cholesterol-Lowering Medication Repatha™ (evolocumab), The First PCSK9 Inhibitor To Be Approved In The World, For Treatment Of High Cholesterol</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 22. Juli 2015 im Webarchiv <i><a href="Archive.today" title="Archive.today">archive.today</a></i>), Amgen-Pressemitteilung vom 21. Juli 2015</span>
</li>
<li id="cite_note-13"><span class="mw-cite-backlink"><a href="#cite_ref-13">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20151123110119/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2114179">European Commission Approves Kyprolis® (carfilzomib) For Combination Use In The Treatment Of Patients With Relapsed Multiple Myeloma</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 23. November 2015 im <i><a href="Internet_Archive" title="Internet Archive">Internet Archive</a></i>), PM AMGEN vom 19. November 2015, abgerufen am 20. November 2015</span>
</li>
<li id="cite_note-PMAMG25092015-ENG-14"><span class="mw-cite-backlink"><a href="#cite_ref-PMAMG25092015-ENG_14-0">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/news-releases/2015/09/amgen-receives-chmp-positive-opinions-for-two-new-treatment-options-for-patients-with-blood-cancer-in-europe/">Amgen Receives CHMP Positive Opinions For Two New Treatment Options For Patients With Blood Cancer In Europe</a>, PM AMGEN vom 25. September 2015, abgerufen am 9. November 2015</span>
</li>
<li id="cite_note-15"><span class="mw-cite-backlink"><a href="#cite_ref-15">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm455873.htm">FDA approved carfilzomib (Kyprolis, Onyx Pharmaceuticals, Inc., an Amgen subsidiary)</a>, Meldung der FDA vom 24. Juli 2015, abgerufen am 9. November 2015</span>
</li>
<li id="cite_note-PM-Amgen-2116999-16"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-PM-Amgen-2116999_16-0">a</a></sup> <sup><a href="#cite_ref-PM-Amgen-2116999_16-1">b</a></sup> <sup><a href="#cite_ref-PM-Amgen-2116999_16-2">c</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20151124104203/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2116999">European Commission Approves Amgen’s BLINCYTO® (blinatumomab) for the Treatment of Adults with Philadelphia Chromosome-Negative Relapsed or Refractory B-precursor Acute Lymphoblastic Leukemia</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 24. November 2015 im <i><a href="Internet_Archive" title="Internet Archive">Internet Archive</a></i>), PM Amgen vom 24. November 2015, abgerufen am 24. November 2015</span>
</li>
<li id="cite_note-PM-FDA-425597-17"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-PM-FDA-425597_17-0">a</a></sup> <sup><a href="#cite_ref-PM-FDA-425597_17-1">b</a></sup> <sup><a href="#cite_ref-PM-FDA-425597_17-2">c</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm425597.htm">Blinatumomab</a>, Meldung der FDA vom 3. Dezember 2014, abgerufen am 24. November 2015</span>
</li>
<li id="cite_note-18"><span class="mw-cite-backlink"><a href="#cite_ref-18">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=1994704">FDA Approves BLINCYTO™ (Blinatumomab) Immunotherapy for the Treatment of Relapsed or Refractory B-Cell Precursor Acute Lymphoblastic Leukemia, PM Amgen vom 3. Dezember 2015, abgerufen am 24. November 2015</a></span>
</li>
<li id="cite_note-19"><span class="mw-cite-backlink"><a href="#cite_ref-19">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://www.amgen.com/newsroom/press-releases/2017/07/fda-grants-full-approval-for-blincyto-blinatumomab-to-treat-relapsed-or-refractory-bcell-precursor-acute-lymphoblastic-leukemia-in-adults-and-children"><i>FDA Grants Full Approval for BLINCYTO® (blinatumomab) to Treat Relapsed or Refractory B-cell Precursor Acute Lymphoblastic Leukemia in Adults and Children.</i></a> In: <i>PM Amgen.</i> 11.&nbsp;Juli 2017,<span class="Abrufdatum"> abgerufen am 21.&nbsp;März 2023</span> (englisch).</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&amp;rfr_id=info%3Asid%2Fde.wikipedia.org%3AAmgen&amp;rft.title=FDA+Grants+Full+Approval+for+BLINCYTO%C2%AE+%28blinatumomab%29+to+Treat+Relapsed+or+Refractory+B-cell+Precursor+Acute+Lymphoblastic+Leukemia+in+Adults+and+Children&amp;rft.description=FDA+Grants+Full+Approval+for+BLINCYTO%C2%AE+%28blinatumomab%29+to+Treat+Relapsed+or+Refractory+B-cell+Precursor+Acute+Lymphoblastic+Leukemia+in+Adults+and+Children&amp;rft.identifier=https%3A%2F%2Fwww.amgen.com%2Fnewsroom%2Fpress-releases%2F2017%2F07%2Ffda-grants-full-approval-for-blincyto-blinatumomab-to-treat-relapsed-or-refractory-bcell-precursor-acute-lymphoblastic-leukemia-in-adults-and-children&amp;rft.date=2017-07-11&amp;rft.language=en">&nbsp;</span></span>
</li>
<li id="cite_note-EU-Zulassung_T-Vec-20"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-EU-Zulassung_T-Vec_20-0">a</a></sup> <sup><a href="#cite_ref-EU-Zulassung_T-Vec_20-1">b</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20151223212953/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2123914">European Commission Approves Amgen’s IMLYGIC™ (talimogene laherparepvec) As First Oncolytic Immunotherapy In Europe</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 23. Dezember 2015 im <i><a href="Internet_Archive" title="Internet Archive">Internet Archive</a></i>), PM Amgen vom 17. Dezember 2015, abgerufen am 21. Dezember 2015</span>
</li>
<li id="cite_note-CHMP_T-Vec-21"><span class="mw-cite-backlink"><a href="#cite_ref-CHMP_T-Vec_21-0">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.ema.europa.eu/ema/index.jsp?curl=pages/news_and_events/news/2015/10/news_detail_002421.jsp&amp;mid=WC0b01ac058004d5c1">First oncolytic immunotherapy medicine recommended for approval</a>, Meldung der EMA vom 21. Oktober 2015, abgerufen am 8. November 2015</span>
</li>
<li id="cite_note-22"><span class="mw-cite-backlink"><a href="#cite_ref-22">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/news-releases/2015/10/fda-approves-imlygic-talimogene-laherparepvec-as-first-oncolytic-viral-therapy-in-the-us/">FDA Approves IMLYGIC™ (Talimogene Laherparepvec) As First Oncolytic Viral Therapy In The US</a>, PM Amgen vom 27. Oktober 2015, abgerufen am 8. November 2015</span>
</li>
<li id="cite_note-melanoma-23"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-melanoma_23-0">a</a></sup> <sup><a href="#cite_ref-melanoma_23-1">b</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/media_pr_detail.jsp?releaseID=1896999"><i>Amgen And Merck Announce Collaboration To Evaluate Investigational Combination Treatment For Advanced Melanoma</i>.</a> Pressemeldung Amgen vom 5. Februar 2014</span>
</li>
<li id="cite_note-24"><span class="mw-cite-backlink"><a href="#cite_ref-24">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/news-releases/2016/11/european-commission-approves-parsabiv-etelcalcetide-for-the-treatment-of-secondary-hyperparathyroidism-in-adults-on-hemodialysis/">European Commission Approves Parsabiv™ (etelcalcetide) For The Treatment Of Secondary Hyperparathyroidism In Adults On Hemodialysis</a>, PM Amgen vom 11. November 2016, abgerufen am 9. Juni 2017</span>
</li>
<li id="cite_note-25"><span class="mw-cite-backlink"><a href="#cite_ref-25">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/003995/human_med_002037.jsp&amp;mid=WC0b01ac058001d124">European public assessment report (EPAR)</a>, EMA, abgerufen am 9. Juni 2017</span>
</li>
<li id="cite_note-26"><span class="mw-cite-backlink"><a href="#cite_ref-26">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.ema.europa.eu/docs/de_DE/document_library/EPAR_-_Summary_for_the_public/human/003995/WC500217050.pdf">Zusammenfassung des EPAR für die Öffentlichkeit</a> (PDF) EMA, abgerufen am 9. Juni 2017</span>
</li>
<li id="cite_note-amgevita-27"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-amgevita_27-0">a</a></sup> <sup><a href="#cite_ref-amgevita_27-1">b</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2256174">European Commission Approves AMGEVITA™ (Biosimilar Adalimumab) For The Treatment Of Certain Inflammatory Diseases</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2256174">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2256174">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2256174">Suche in Webarchiven</a>)</small>, PM Amgen vom 23. März 2017, abgerufen am 12. April 2017</span>
</li>
<li id="cite_note-28"><span class="mw-cite-backlink"><a href="#cite_ref-28">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2349784">FDA Approves Aimovig™ (erenumab-aooe), A Novel Treatment Developed Specifically For Migraine Prevention</a>,PM Amgen vom 17. Mai 2018, abgerufen am 19. Mai 2018</span>
</li>
<li id="cite_note-29"><span class="mw-cite-backlink"><a href="#cite_ref-29">↑</a></span> <span class="reference-text">Multimedia News Release: <a rel="nofollow" class="external text" href="https://web.archive.org/web/20180518072102/https://www.multivu.com/players/English/8004556-amgen-aimovig-fda-approval/">FDA Approves Aimovig</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 18. Mai 2018 im <i><a href="Internet_Archive" title="Internet Archive">Internet Archive</a></i>)</span>
</li>
<li id="cite_note-30"><span class="mw-cite-backlink"><a href="#cite_ref-30">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.novartis.com/news/media-releases/novartis-and-amgen-announce-fda-approval-aimovigtm-erenumab-novel-treatment-developed-specifically-migraine-prevention">Novartis and Amgen announce FDA approval of Aimovig(TM) (erenumab), a novel treatment developed specifically for migraine prevention</a>, PM Novartis vom 18. Mai 2018, abgerufen am 19. Mai 2018</span>
</li>
<li id="cite_note-31"><span class="mw-cite-backlink"><a href="#cite_ref-31">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.ema.europa.eu/docs/de_DE/document_library/EPAR_-_Summary_for_the_public/human/004447/WC500253557.pdf">Übersicht über Aimovig und Begründung für die Zulassung in der EU</a> (PDF) EMA, abgerufen am 10. September 2018</span>
</li>
<li id="cite_note-32"><span class="mw-cite-backlink"><a href="#cite_ref-32">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.novartis.com/news/media-releases/novartis-marks-new-era-migraine-patients-eu-approval-aimovigr-first-its-kind-treatment-specifically-designed-migraine-prevention">Novartis marks a new era for migraine patients with the EU approval of Aimovig®, a first-of-its-kind treatment specifically designed for migraine prevention</a>, PM Novartis vom 30. Juli 2018</span>
</li>
<li id="cite_note-FDA_Romosozumab-33"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-FDA_Romosozumab_33-0">a</a></sup> <sup><a href="#cite_ref-FDA_Romosozumab_33-1">b</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=2394009">FDA Approves EVENITY™ (romosozumab-aqqg) For The Treatment Of Osteoporosis In Postmenopausal Women At High Risk For Fracture</a>, PM Amgen vom 9. April 2019, abgerufen am 14. April 2019</span>
</li>
<li id="cite_note-pipeline-34"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-pipeline_34-0">a</a></sup> <sup><a href="#cite_ref-pipeline_34-1">b</a></sup> <sup><a href="#cite_ref-pipeline_34-2">c</a></sup> <sup><a href="#cite_ref-pipeline_34-3">d</a></sup> <sup><a href="#cite_ref-pipeline_34-4">e</a></sup></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.amgenpipeline.com/pipeline/">Amgen Pipeline</a> Übersicht der in der <a href="Produktpipeline" title="Produktpipeline">Pipeline</a> befindlichen Medikamente</span>
</li>
<li id="cite_note-35"><span class="mw-cite-backlink"><a href="#cite_ref-35">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.ema.europa.eu/en/news/meeting-highlights-committee-medicinal-products-human-use-chmp-14-17-october-2019">Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 14-17 October 2019</a>, PM EMA vom 18. Oktober 2019, abgerufen am 29. Oktober 2019</span>
</li>
<li id="cite_note-iqwig.de-36"><span class="mw-cite-backlink"><a href="#cite_ref-iqwig.de_36-0">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://www.iqwig.de/de/presse/pressemitteilungen/2020/romosozumab-bei-osteoporose-betraechtlicher-zusatznutzen-fuer-frauen-nach-der-menopause.13079.html"><i>Romosozumab bei Osteoporose: Beträchtlicher Zusatznutzen für Frauen nach der Menopause.</i></a> IQWiG, 15.&nbsp;Juni 2020,<span class="Abrufdatum"> abgerufen am 2.&nbsp;Juli 2020</span>.</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&amp;rfr_id=info%3Asid%2Fde.wikipedia.org%3AAmgen&amp;rft.title=Romosozumab+bei+Osteoporose%3A+Betr%C3%A4chtlicher+Zusatznutzen+f%C3%BCr+Frauen+nach+der+Menopause&amp;rft.description=Romosozumab+bei+Osteoporose%3A+Betr%C3%A4chtlicher+Zusatznutzen+f%C3%BCr+Frauen+nach+der+Menopause&amp;rft.identifier=https%3A%2F%2Fwww.iqwig.de%2Fde%2Fpresse%2Fpressemitteilungen%2F2020%2Fromosozumab-bei-osteoporose-betraechtlicher-zusatznutzen-fuer-frauen-nach-der-menopause.13079.html&amp;rft.publisher=IQWiG&amp;rft.date=2020-06-15">&nbsp;</span></span>
</li>
<li id="cite_note-37"><span class="mw-cite-backlink"><a href="#cite_ref-37">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.deutsche-apotheker-zeitung.de/news/artikel/2019/08/26/fuer-13-4-milliarden-amgen-will-otezla-rechte-uebernehmen">Für 13,4 Milliarden Dollar: Amgen will Otezla-Rechte übernehmen</a>, DAZ vom 26. August 2019, abgerufen am 18. Mai 2021</span>
</li>
<li id="cite_note-38"><span class="mw-cite-backlink"><a href="#cite_ref-38">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.ema.europa.eu/en/medicines/human/EPAR/otezla#authorisation-details-section">Authorisation details</a>, EPAR der EMA, abgerufen am 18. Mai 2021 </span>
</li>
<li id="cite_note-FDA-20210528-39"><span class="mw-cite-backlink"><a href="#cite_ref-FDA-20210528_39-0">↑</a></span> <span class="reference-text"><i><a rel="nofollow" class="external text" href="https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-sotorasib-kras-g12c-mutated-nsclc">FDA grants accelerated approval to sotorasib for KRAS G12C mutated NSCLC</a></i>, FDA, 28. Mai 2021, abgerufen am 13. September 2021.</span>
</li>
<li id="cite_note-40"><span class="mw-cite-backlink"><a href="#cite_ref-40">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/newsroom/press-releases/2022/01/european-commission-approves-lumykras-sotorasib-for-patients-with-kras-g12cmutated-advanced-nonsmall-cell-lung-cancer">EUROPEAN COMMISSION APPROVES LUMYKRAS® (SOTORASIB) FOR PATIENTS WITH KRAS G12C-MUTATED ADVANCED NON-SMALL CELL LUNG CANCER</a>, PM Amgen vom 9. Januar 2022, abgerufen am 16. Juni 2023</span>
</li>
<li id="cite_note-41"><span class="mw-cite-backlink"><a href="#cite_ref-41">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2366515">Tezepelumab Granted Breakthrough Therapy Designation By US FDA For The Treatment Of Patients With Severe Asthma Without An Eosinophilic Phenotype</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2366515">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2366515">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2366515">Suche in Webarchiven</a>)</small>, PM Amgen vom 6. September 2018, abgerufen am 10. September 2018</span>
</li>
<li id="cite_note-42"><span class="mw-cite-backlink"><a href="#cite_ref-42">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=1975377">Amgen Announces Positive Top-Line Results From Phase 3 Study Evaluating The Efficacy And Safety Of Biosimilar Candidate ABP 501 Compared With Adalimumab In Patients With Moderate-To-Severe Plaque Psoriasis</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=1975377">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=1975377">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=1975377">Suche in Webarchiven</a>)</small>, PM von Amgen vom 8. Oktober 2014, abgerufen am 9. Oktober 2014</span>
</li>
<li id="cite_note-43"><span class="mw-cite-backlink"><a href="#cite_ref-43">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110781">Amgen Presents Detailed Results From Phase 3 Study Demonstrating Clinical Equivalence Of Biosimilar Candidate ABP 501 With Adalimumab</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110781">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110781">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110781">Suche in Webarchiven</a>)</small>, PM AMGEN vom 9. November 2015, abgerufen am 10. November 2015</span>
</li>
<li id="cite_note-44"><span class="mw-cite-backlink"><a href="#cite_ref-44">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgenbiosimilars.com/our-products/approved-products/">Approved Products.</a> WebSite Amgen Biosimilars (englisch) abgerufen am 7. Juni 2017</span>
</li>
<li id="cite_note-45"><span class="mw-cite-backlink"><a href="#cite_ref-45">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.deutsche-apotheker-zeitung.de/news/artikel/2017/01/27/zulassungsempfehlung-des-chmp">Adalimumab-Biosimilars zur Zulassung empfohlen.</a> In: <i>DAZ</i>, 27. Januar 2017; abgerufen am 7. Juni 2017</span>
</li>
<li id="cite_note-46"><span class="mw-cite-backlink"><a href="#cite_ref-46">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgenbiosimilars.com/our-products/our-pipeline/">Our Pipeline.</a> WebSite Amgen Biosimilars (englisch) abgerufen am 7. Juni 2017</span>
</li>
<li id="cite_note-47"><span class="mw-cite-backlink"><a href="#cite_ref-47">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/news-releases/2007/01/cytokinetics-and-amgen-announce-strategic-alliance-in-heart-failure/">Cytokinetics and Amgen Announce Strategic Alliance in Heart Failure</a>, PM Amgen vom 3. Januar 2007, abgerufen am 10. November 2015</span>
</li>
<li id="cite_note-48"><span class="mw-cite-backlink"><a href="#cite_ref-48">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110197">Amgen And Cytokinetics Announce Late-Breaking Presentation Of COSMIC-HF Trial At AHA Scientific Sessions 2015</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110197">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110197">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2110197">Suche in Webarchiven</a>)</small>, PM Amgen vom 8. November 2015, abgerufen am 10. November 2015</span>
</li>
<li id="cite_note-UCB-49"><span class="mw-cite-backlink"><a href="#cite_ref-UCB_49-0">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://wwwext.amgen.com/media/media_pr_detail.jsp?year=2011&amp;releaseID=1582277"><i>Amgen and UCB Team Up With NASA on Final Space Shuttle Mission to Conduct Preclinical Test of Sclerostin Antibody on Bone Loss</i>.</a> Pressemeldung Amgen vom 5. Juli 2011</span>
</li>
<li id="cite_note-50"><span class="mw-cite-backlink"><a href="#cite_ref-50">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299800">EVENITY™ (romosozumab) ARCH Study Results Published In The New England Journal Of Medicine</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299800">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299800">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299800">Suche in Webarchiven</a>)</small>, PM Amgen vom 11. September 2017, abgerufen am 13. September 2017</span>
</li>
<li id="cite_note-51"><span class="mw-cite-backlink"><a href="#cite_ref-51">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=2382691">EVENITY™ (romosozumab) Receives Approval In Japan For The Treatment Of Osteoporosis In Patients At High Risk Of Fracture</a>, PM Amgen vom 8. Januar 2019, abgerufen am 15. Januar 2019</span>
</li>
<li id="cite_note-52"><span class="mw-cite-backlink"><a href="#cite_ref-52">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.astellas.com/jp/en/news/20091">EVENITY® SUBCUTANEOUS INJECTION 105mg SYRINGE RECEIVES THE-FIRST-IN-THE-WORLD APPROVAL IN JAPAN FOR THE TREATMENT OF OSTEOPOROSIS AT HIGH RISK OF FRACTURE</a>, PM Astellas vom 9. Januar 2019, abgerufen am 17. Januar 2019</span>
</li>
<li id="cite_note-53"><span class="mw-cite-backlink"><a href="#cite_ref-53">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=2383654">Amgen And UCB Receive Positive Vote From FDA Advisory Committee In Favor Of Approval For EVENITY™ (romosozumab)</a>, PM Amgen vom 16. Januar 2019, abgerufen am 17. Januar 2019</span>
</li>
<li id="cite_note-54"><span class="mw-cite-backlink"><a href="#cite_ref-54">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.amgen.com/media/media_pr_detail.jsp?year=2012&amp;releaseID=1679295"><i>Amgen and AstraZeneca Announce Collaboration to Jointly Develop and Commercialize Clinical-Stage Inflammation Portfolio</i>.</a> Pressemeldung Amgen vom 2. April 2012</span>
</li>
<li id="cite_note-55"><span class="mw-cite-backlink"><a href="#cite_ref-55">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/news-releases/2015/05/amgen-to-terminate-participation-in-co-development-and-commercialization-of-brodalumab/">Amgen to Terminate Participation in Co-development and Commercialization of Brodalumab</a>, PM Amgen vom 22. Mai 2015, abgerufen am 8. November 2015</span>
</li>
<li id="cite_note-56"><span class="mw-cite-backlink"><a href="#cite_ref-56">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.bloomberg.com/news/2012-04-25/amgen-to-acquire-mustafa-nevzat-to-tap-growth-in-turkey-3-.html">Amgen to Acquire Mustafa Nevzat</a></span>
</li>
<li id="cite_note-57"><span class="mw-cite-backlink"><a href="#cite_ref-57">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/media_pr_detail.jsp?releaseID=1765710"><i>Amgen to Acquire deCODE Genetics, a Global Leader in Human Genetics</i>.</a> Pressemeldung Amgen vom 10. Dezember 2012</span>
</li>
<li id="cite_note-58"><span class="mw-cite-backlink"><a href="#cite_ref-58">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=1849611&amp;highlight="><i>Amgen To Acquire Onyx Pharmaceuticals For $125 Per Share In Cash</i>.</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=1849611&amp;highlight=">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=1849611&amp;highlight=">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=1849611&amp;highlight=">Suche in Webarchiven</a>)</small> Pressemeldung Amgen vom 25. August 2013</span>
</li>
<li id="cite_note-59"><span class="mw-cite-backlink"><a href="#cite_ref-59">↑</a></span> <span class="reference-text">Pressemeldung Onyx vom 25. August 2013: <a rel="nofollow" class="external text" href="https://web.archive.org/web/20130829024800/http://www.onyx.com/view.cfm/686/amgen-to-acquire-onyx-pharmaceuticals-for-125-per-share-in-cash">Amgen To Acquire Onyx Pharmaceuticals For $125 Per Share In Cash</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 29. August 2013 im <i><a href="Internet_Archive" title="Internet Archive">Internet Archive</a></i>)</span>
</li>
<li id="cite_note-60"><span class="mw-cite-backlink"><a href="#cite_ref-60">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.pharmazeutische-zeitung.de/index.php?id=64101">T-Vec: Onkolytische Immuntherapie auf dem Markt</a> Pharmazeutische Zeitung vom 1. Juli 2016, abgerufen am 3. Februar 2017</span>
</li>
<li id="cite_note-61"><span class="mw-cite-backlink"><a href="#cite_ref-61">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.com/media/news-releases/2016/09/amgen-and-servier-extend-omecamtiv-mecarbil-collaboration-in-chronic-heart-failure/">Amgen And Servier Extend Omecamtiv Mecarbil Collaboration In Chronic Heart Failure</a>, PM Amgen vom 1. September 2016, abgerufen am 8. Juni 2017</span>
</li>
<li id="cite_note-62"><span class="mw-cite-backlink"><a href="#cite_ref-62">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=2264168">Amgen Announces Expanded Commercial Collaboration With Novartis For Erenumab In Migraine</a>, PM Amgen vom 24. April 2017, abgerufen am 11. Mai 2017</span>
</li>
<li id="cite_note-63"><span class="mw-cite-backlink"><a href="#cite_ref-63">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.novartis.com/news/media-releases/novartis-expands-global-collaboration-amgen-commercialize-first-class-amg-334">Novartis expands global collaboration with Amgen to commercialize first-in-class AMG 334 (erenumab) program in migraine prevention in the US and Canada</a>, PM Novartis vom 24. April 2017, abgerufen am 11. Mai 2017</span>
</li>
<li id="cite_note-64"><span class="mw-cite-backlink"><a href="#cite_ref-64">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299326">New Data Demonstrate Aimovig™ (erenumab) Reduced Monthly Migraine Days In Patients Who Failed Previous Preventive Therapies</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299326">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299326">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2299326">Suche in Webarchiven</a>)</small>, PM Amgen vom 7. September 2017, abgerufen am 10. September 2017</span>
</li>
<li id="cite_note-65"><span class="mw-cite-backlink"><a href="#cite_ref-65">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2279526">Amgen And Allergan Announce FDA Advisory Committee Meeting To Review ABP 215, A Biosimilar Candidate To Bevacizumab.</a><span style="display:none"><a rel="nofollow" class="external text" href="http://deadurl.invalid/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2279526">@1</a></span><span style="display:none"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2279526">@2</a></span><span style="display:none">Vorlage:Toter Link/investors.amgen.com</span> <small>(Seite dauerhaft nicht mehr abrufbar, festgestellt im Juni 2023. <a rel="nofollow" class="external text" href="http://timetravel.mementoweb.org/list/2010/http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=RssLanding&amp;cat=news&amp;id=2279526">Suche in Webarchiven</a>)</small> PM Amgen, 7. Juni 2017 (englisch) abgerufen am 7. Juni 2017</span>
</li>
<li id="cite_note-66"><span class="mw-cite-backlink"><a href="#cite_ref-66">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://investors.amgen.com/phoenix.zhtml?c=61656&amp;p=irol-newsArticle&amp;ID=2304434">Amgen And CytomX Therapeutics Announce Strategic Collaboration In Immuno-Oncology</a>, PM Amgen vom 3. Oktober 2017, abgerufen am 6. Oktober 2017</span>
</li>
<li id="cite_note-67"><span class="mw-cite-backlink"><a href="#cite_ref-67">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.prnewswire.com/news-releases/amgen-to-acquire-five-prime-therapeutics-for-1-9-billion-in-cash-301240358.html">Amgen To Acquire Five Prime Therapeutics For $1.9 Billion in Cash</a>, PM Amgen vom 3. März 2021, abgerufen am 28. März 2021</span>
</li>
<li id="cite_note-68"><span class="mw-cite-backlink"><a href="#cite_ref-68">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://wwwext.amgen.com/newsroom/press-releases/2021/03/amgen-to-acquire-rodeo-therapeutics-corporation">Amgen to Acquire Rodeo Therapeutics Corporation</a>, PM Amgen vom 30. März 2021, abgerufen am 31. März 2021</span>
</li>
<li id="cite_note-69"><span class="mw-cite-backlink"><a href="#cite_ref-69">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://wwwext.amgen.com/newsroom/press-releases/2022/12/rule-2-7-announcement-amgen-inc-to-acquire-horizon-therapeutics-plc">Amgen Inc to Acquire Horizon Therapeutics plc</a>, PM Amgen vom 12. Dezember 2022, abgerufen am 18. Januar 2023</span>
</li>
<li id="cite_note-70"><span class="mw-cite-backlink"><a href="#cite_ref-70">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.handelsblatt.com/unternehmen/industrie/arzneimittelbranche-groesste-pharma-uebernahme-des-jahres-amgen-will-horizon-fuer-28-milliarden-dollar-uebernehmen/28862458.html">Größte Pharma-Übernahme des Jahres</a>, Handelsblatt vom 12. Dezember 2022, abgerufen am 18. Januar 2023</span>
</li>
<li id="cite_note-71"><span class="mw-cite-backlink"><a href="#cite_ref-71">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.amgen.de/medien/news/617/amgen-schliesst-uebernahme-von-horizon-therapeutics-ab/">Amgen schließt die Übernahme von Horizon Therapeutics ab</a>, PM Amgen vom 6. Oktober 2023, abgerufen am 26. Februar 2024</span>
</li>
<li id="cite_note-72"><span class="mw-cite-backlink"><a href="#cite_ref-72">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20130524080650/http://www.amgen.de/Amgen/Factsheets/index.html">Amgen Facts: Mitarbeiter, Umsatz, Forschung &amp; Entwicklung</a> (<span class="webarchiv-memento"><a href="Webarchivierung#Begrifflichkeiten" title="Webarchivierung">Memento</a></span> vom 24. Mai 2013 im <i><a href="Internet_Archive" title="Internet Archive">Internet Archive</a></i>), abgerufen am 27. November 2012</span>
</li>
<li id="cite_note-73"><span class="mw-cite-backlink"><a href="#cite_ref-73">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20170319195950/https://www.amgen.de/Presse/Uebersicht/Amgen-in-D-Factsheet-dt-20150505.pdf"><i>Amgen in Deutschland.</i></a> (PDF; 5,4&nbsp;MB) In: <i>amgen.de.</i> Mai 2015, archiviert vom <style data-mw-deduplicate="TemplateStyles:r250917974">
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</style><span class="dewiki-iconexternal"><a class="external text" href="https://redirecter.toolforge.org/?url=https%3A%2F%2Fwww.amgen.de%2FPresse%2FUebersicht%2FAmgen-in-D-Factsheet-dt-20150505.pdf">Original</a></span> (nicht mehr online verfügbar) am <span style="white-space:nowrap;">19.&nbsp;März 2017</span><span>;</span><span class="Abrufdatum"> abgerufen am 18.&nbsp;Januar 2021</span>.</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&amp;rfr_id=info%3Asid%2Fde.wikipedia.org%3AAmgen&amp;rft.title=Amgen+in+Deutschland&amp;rft.description=Amgen+in+Deutschland&amp;rft.identifier=https%3A%2F%2Fweb.archive.org%2Fweb%2F20170319195950%2Fhttps%3A%2F%2Fwww.amgen.de%2FPresse%2FUebersicht%2FAmgen-in-D-Factsheet-dt-20150505.pdf&amp;rft.date=2015-05&amp;rft.source=https://www.amgen.de/Presse/Uebersicht/Amgen-in-D-Factsheet-dt-20150505.pdf">&nbsp;</span></span>
</li>
<li id="cite_note-74"><span class="mw-cite-backlink"><a href="#cite_ref-74">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.springerfachmedien-medizin.de/galenus-preise-2011-vergeben/882912.html"><i>Galenus-von-Pergamon-Preis 2011 für drei Spitzenleistungen in der Pharmakologie vergeben</i>.</a> Pressemeldung von Springer Medizin</span>
</li>
<li id="cite_note-75"><span class="mw-cite-backlink"><a href="#cite_ref-75">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.pharmazeutische-zeitung.de/2017-12/knochendichte-reboundeffekt-nach-absetzen-von-denosumab/"><i>Knochendichte: Reboundeffekt nach Absetzen von Denosumab.</i></a> In: <a href="Pharmazeutische_Zeitung" title="Pharmazeutische Zeitung">Pharmazeutische Zeitung</a> vom 1. Dezember 2017.</span>
</li>
<li id="cite_note-76"><span class="mw-cite-backlink"><a href="#cite_ref-76">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://www.aerzteblatt.de/archiv/195014/Arznei%C2%ADmittel%C2%ADkommission-der-Deutschen-Aerzteschaft-Aus-der-UAW-Datenbank-Multiple-Wirbelkoerperfrakturen-nach-Absetzen-von-Denosumab-(Prolia-)"><i>Arzneimittelkommission der Deutschen Ärzteschaft: „Aus der UAW-Datenbank“ – Multiple Wirbelkörperfrakturen nach Absetzen von Denosumab (Prolia ® )</i>.</a> In: <i><a href="Deutsches_%C3%84rzteblatt" title="Deutsches Ärzteblatt">Deutsches Ärzteblatt</a></i>, 2017, 114(48), S. A-2309 / B-1933 / C-1887.</span>
</li>
<li id="cite_note-77"><span class="mw-cite-backlink"><a href="#cite_ref-77">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://www.rheumaliga.ch/blog/2018/prolia-osteoporose"><i>Prolia® – Osteoporose-Medikament mit Risiken?</i></a> Rheumaliga Schweiz,<span class="Abrufdatum"> abgerufen am 14.&nbsp;Juni 2022</span>.</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&amp;rfr_id=info%3Asid%2Fde.wikipedia.org%3AAmgen&amp;rft.title=Prolia%C2%AE+%E2%80%93+Osteoporose-Medikament+mit+Risiken%3F&amp;rft.description=Prolia%C2%AE+%E2%80%93+Osteoporose-Medikament+mit+Risiken%3F&amp;rft.identifier=https%3A%2F%2Fwww.rheumaliga.ch%2Fblog%2F2018%2Fprolia-osteoporose&amp;rft.publisher=Rheumaliga+Schweiz">&nbsp;</span></span>
</li>
<li id="cite_note-78"><span class="mw-cite-backlink"><a href="#cite_ref-78">↑</a></span> <span class="reference-text"><span class="cite"><a rel="nofollow" class="external text" href="https://compendium.ch/mpro/mnr/21793/html/de"><i>Prolia®.</i></a> Fachinformation des Arzneimittel-Kompendium der Schweiz®. Amgen Switzerland AG, 15.&nbsp;April 2019,<span class="Abrufdatum"> abgerufen am 14.&nbsp;Juni 2022</span>.</span><span style="display: none;" class="Z3988" title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&amp;rfr_id=info%3Asid%2Fde.wikipedia.org%3AAmgen&amp;rft.title=Prolia%C2%AE&amp;rft.description=Prolia%C2%AE&amp;rft.identifier=https%3A%2F%2Fcompendium.ch%2Fmpro%2Fmnr%2F21793%2Fhtml%2Fde&amp;rft.publisher=Amgen+Switzerland+AG&amp;rft.date=2019-04-15">&nbsp;</span></span>
</li>
<li id="cite_note-79"><span class="mw-cite-backlink"><a href="#cite_ref-79">↑</a></span> <span class="reference-text">Gordon Binder (* 1935) war ab 1982 Chief Financial Officer und 1988 bis 2000 CEO und Chairman von Amgen</span>
</li>
</ol></div>
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<a href="MercadoLibre" title="MercadoLibre">MercadoLibre</a>&nbsp;|
<a href="Meta_Platforms" title="Meta Platforms">Meta Platforms</a>&nbsp;|
<a href="Microchip_Technology" title="Microchip Technology">Microchip Technology</a>&nbsp;|
<a href="Micron_Technology" title="Micron Technology">Micron Technology</a>&nbsp;|
<a href="Microsoft" title="Microsoft">Microsoft</a>&nbsp;|
<a href="Mondelez_International" title="Mondelez International">Mondelez International</a>&nbsp;|
<a href="Monolithic_Power_Systems" title="Monolithic Power Systems">Monolithic Power Systems</a>&nbsp;|
<a href="Monster_Beverage" title="Monster Beverage">Monster Beverage</a>&nbsp;|
<a href="Netflix" title="Netflix">Netflix</a>&nbsp;|
<a href="Nvidia" title="Nvidia">Nvidia</a>&nbsp;|
<a href="NXP_Semiconductors" title="NXP Semiconductors">NXP Semiconductors</a>&nbsp;|
<a href="Old_Dominion_Freight_Line" title="Old Dominion Freight Line">Old Dominion Freight Line</a>&nbsp;|
<a href="O%E2%80%99Reilly_Auto_Parts" title="O’Reilly Auto Parts">O’Reilly Auto Parts</a>&nbsp;|
<a href="Paccar" title="Paccar">Paccar</a>&nbsp;|
<a href="Palantir_Technologies" title="Palantir Technologies">Palantir Technologies</a>&nbsp;|
<a href="Palo_Alto_Networks" title="Palo Alto Networks">Palo Alto Networks</a>&nbsp;|
<a href="Paychex" title="Paychex">Paychex</a>&nbsp;|
<a href="PayPal" title="PayPal">PayPal</a>&nbsp;|
<a href="PepsiCo" title="PepsiCo">PepsiCo</a>&nbsp;|
<a href="Pinduoduo" title="Pinduoduo">Pinduoduo</a>&nbsp;|
<a href="Qualcomm" title="Qualcomm">Qualcomm</a>&nbsp;|
<a href="Regeneron_Pharmaceuticals" title="Regeneron Pharmaceuticals">Regeneron Pharmaceuticals</a>&nbsp;|
<a href="Roper_Technologies" title="Roper Technologies">Roper Technologies</a>&nbsp;|
<a href="Ross_Stores" title="Ross Stores">Ross Stores</a>&nbsp;|
<a href="Seagate_Technology" title="Seagate Technology">Seagate Technology</a>&nbsp;|
<a href="Shopify" title="Shopify">Shopify</a>&nbsp;|
<a href="Solstice_Advanced_Materials" class="mw-redirect" title="Solstice Advanced Materials">Solstice Advanced Materials</a>&nbsp;|
<a href="Starbucks" title="Starbucks">Starbucks</a>&nbsp;|
<a href="Strategy_Inc" title="Strategy Inc">Strategy</a>&nbsp;|
<a href="Synopsys" title="Synopsys">Synopsys</a>&nbsp;|
<a href="Take_2_Interactive" title="Take 2 Interactive">Take 2 Interactive</a>&nbsp;|
<a href="Tesla%2C_Inc." title="Tesla, Inc.">Tesla</a>&nbsp;|
<a href="Texas_Instruments" title="Texas Instruments">Texas Instruments</a>&nbsp;|
<a href="Thomson_Reuters" title="Thomson Reuters">Thomson Reuters</a>&nbsp;|
<a href="T-Mobile_US" title="T-Mobile US">T-Mobile US</a>&nbsp;|
<a href="Verisk_Analytics" title="Verisk Analytics">Verisk Analytics</a>&nbsp;|
<a href="Vertex_Pharmaceuticals" title="Vertex Pharmaceuticals">Vertex Pharmaceuticals</a>&nbsp;|
<a href="Warner_Bros._Discovery" title="Warner Bros. Discovery">Warner Bros. Discovery</a>&nbsp;|
<a href="Western_Digital" title="Western Digital">Western Digital</a>&nbsp;|
<a href="Workday" title="Workday">Workday</a>&nbsp;|
<a href="Xcel_Energy" title="Xcel Energy">Xcel Energy</a>&nbsp;|
<a href="Zscaler" title="Zscaler">Zscaler</a>
</p>
</div>
</div></div>
<div class="klappleiste mw-collapsible navileiste navigation-not-searchable center" role="navigation">
<div class="klappleiste-bild nomobile noviewer" aria-hidden="true" role="presentation"><span typeof="mw:File"></span></div>
<div class="klappleiste-kopf">Unternehmen im <a href="S%26P_100" title="S&amp;P 100">S&amp;P 100</a> <small>(Stand: 19. September 2025)</small></div>
<div class="klappleiste-inhalt mw-collapsible-content">
<div class="centered" style="display: table">
<p><a href="3M" title="3M">3M</a>&nbsp;|
<a href="Abbott_Laboratories" title="Abbott Laboratories">Abbott Laboratories</a>&nbsp;|
<a href="Abbvie" title="Abbvie">Abbvie</a>&nbsp;|
<a href="Accenture" title="Accenture">Accenture</a>&nbsp;|
<a href="Adobe_Inc." title="Adobe Inc.">Adobe Inc.</a>&nbsp;|
<a href="Alphabet_Inc." title="Alphabet Inc.">Alphabet Inc.</a> (Class C)&nbsp;|
<a href="Altria_Group" title="Altria Group">Altria Group</a>&nbsp;|
<a href="Amazon" title="Amazon">Amazon</a>&nbsp;|
<a href="AMD" title="AMD">AMD</a>&nbsp;|
<a href="American_Express" title="American Express">American Express</a>&nbsp;|
<a href="American_International_Group" title="American International Group">American International Group</a>&nbsp;|
<a href="American_Tower" title="American Tower">American Tower</a>&nbsp;|
<a class="mw-selflink selflink">Amgen</a>&nbsp;|
<a href="Apple" title="Apple">Apple</a>&nbsp;|
<a href="AT%26T" title="AT&amp;T">AT&amp;T</a>&nbsp;|
<a href="Bank_of_America" title="Bank of America">Bank of America</a>&nbsp;|
<a href="Bank_of_New_York_Mellon" title="Bank of New York Mellon">Bank of New York Mellon</a>&nbsp;|
<a href="Berkshire_Hathaway" title="Berkshire Hathaway">Berkshire Hathaway</a> (Class B)&nbsp;|
<a href="BlackRock" title="BlackRock">BlackRock</a>&nbsp;|
<a href="Boeing" title="Boeing">Boeing</a>&nbsp;|
<a href="Booking_Holdings" title="Booking Holdings">Booking Holdings</a>&nbsp;|
<a href="Bristol-Myers_Squibb" title="Bristol-Myers Squibb">Bristol-Myers Squibb</a>&nbsp;|
<a href="Broadcom_Inc." title="Broadcom Inc.">Broadcom Inc.</a>&nbsp;|
<a href="Capital_One" title="Capital One">Capital One</a>&nbsp;|
<a href="Caterpillar" title="Caterpillar">Caterpillar</a>&nbsp;|
<a href="Charles_Schwab_Corporation" title="Charles Schwab Corporation">Charles Schwab Corporation</a>&nbsp;|
<a href="Charter_Communications" title="Charter Communications">Charter Communications</a>&nbsp;|
<a href="Chevron_Corporation" title="Chevron Corporation">Chevron Corporation</a>&nbsp;|
<a href="Cisco_Systems" title="Cisco Systems">Cisco Systems</a>&nbsp;|
<a href="Citigroup" title="Citigroup">Citigroup</a>&nbsp;|
<a href="Colgate-Palmolive" title="Colgate-Palmolive">Colgate-Palmolive</a>&nbsp;|
<a href="Comcast" title="Comcast">Comcast</a> (Class A)&nbsp;|
<a href="ConocoPhillips" title="ConocoPhillips">ConocoPhillips</a>&nbsp;|
<a href="Costco_Wholesale" title="Costco Wholesale">Costco Wholesale</a>&nbsp;|
<a href="CVS_Health" title="CVS Health">CVS Health</a>&nbsp;|
<a href="Danaher_Corporation" title="Danaher Corporation">Danaher Corporation</a>&nbsp;|
<a href="Duke_Energy" title="Duke Energy">Duke Energy</a>&nbsp;|
<a href="Eli_Lilly_and_Company" title="Eli Lilly and Company">Eli Lilly and Company</a>&nbsp;|
<a href="Emerson_Electric_Company" title="Emerson Electric Company">Emerson Electric Company</a>&nbsp;|
<a href="ExxonMobil" title="ExxonMobil">ExxonMobil</a>&nbsp;|
<a href="FedEx" title="FedEx">FedEx</a>&nbsp;|
<a href="Ford" title="Ford">Ford</a>&nbsp;|
<a href="GE_Aerospace" title="GE Aerospace">GE Aerospace</a>&nbsp;|
<a href="General_Dynamics" title="General Dynamics">General Dynamics</a>&nbsp;|
<a href="General_Motors" title="General Motors">General Motors</a>&nbsp;|
<a href="Gilead_Sciences" title="Gilead Sciences">Gilead Sciences</a>&nbsp;|
<a href="Goldman_Sachs" title="Goldman Sachs">Goldman Sachs</a>&nbsp;|
<a href="Honeywell_International" title="Honeywell International">Honeywell International</a>&nbsp;|
<a href="IBM" title="IBM">IBM</a>&nbsp;|
<a href="Intel" title="Intel">Intel</a>&nbsp;|
<a href="Intuit" title="Intuit">Intuit</a>&nbsp;|
<a href="Intuitive_Surgical" title="Intuitive Surgical">Intuitive Surgical</a>&nbsp;|
<a href="John_Deere" title="John Deere">John Deere</a>&nbsp;|
<a href="Johnson_%26_Johnson" title="Johnson &amp; Johnson">Johnson &amp; Johnson</a>&nbsp;|
<a href="JPMorgan_Chase" title="JPMorgan Chase">JPMorgan Chase</a>&nbsp;|
<a href="Linde_plc" title="Linde plc">Linde plc</a>&nbsp;|
<a href="Lockheed_Martin" title="Lockheed Martin">Lockheed Martin</a>&nbsp;|
<a href="Lowe%E2%80%99s" title="Lowe’s">Lowe’s</a>&nbsp;|
<a href="Mastercard" title="Mastercard">Mastercard</a> (Class A)&nbsp;|
<a href="McDonald%E2%80%99s" title="McDonald’s">McDonald’s</a>&nbsp;|
<a href="Medtronic" title="Medtronic">Medtronic</a>&nbsp;|
<a href="Merck_%26_Co." title="Merck &amp; Co.">Merck &amp; Co.</a>&nbsp;|
<a href="Meta_Platforms" title="Meta Platforms">Meta Platforms</a> (Class A)&nbsp;|
<a href="Metropolitan_Life_Insurance_Company" title="Metropolitan Life Insurance Company">MetLife Inc.</a>&nbsp;|
<a href="Microsoft" title="Microsoft">Microsoft</a>&nbsp;|
<a href="Mondelez_International" title="Mondelez International">Mondelez International</a>&nbsp;|
<a href="Morgan_Stanley" title="Morgan Stanley">Morgan Stanley</a>&nbsp;|
<a href="Netflix" title="Netflix">Netflix</a>&nbsp;|
<a href="NextEra_Energy" title="NextEra Energy">NextEra Energy</a>&nbsp;|
<a href="Nike_(Unternehmen)" title="Nike (Unternehmen)">Nike (Unternehmen)</a> (Class B)&nbsp;|
<a href="Nvidia" title="Nvidia">Nvidia</a>&nbsp;|
<a href="Oracle" title="Oracle">Oracle</a>&nbsp;|
<a href="Palantir_Technologies" title="Palantir Technologies">Palantir Technologies</a>&nbsp;|
<a href="PayPal" title="PayPal">PayPal</a>&nbsp;|
<a href="PepsiCo" title="PepsiCo">PepsiCo</a>&nbsp;|
<a href="Pfizer" title="Pfizer">Pfizer</a>&nbsp;|
<a href="Philip_Morris_International" title="Philip Morris International">Philip Morris International</a>&nbsp;|
<a href="Procter_%26_Gamble" title="Procter &amp; Gamble">Procter &amp; Gamble</a>&nbsp;|
<a href="Qualcomm" title="Qualcomm">Qualcomm</a>&nbsp;|
<a href="RTX_Corporation" title="RTX Corporation">RTX Corporation</a>&nbsp;|
<a href="Salesforce" title="Salesforce">Salesforce</a>&nbsp;|
<a href="ServiceNow" title="ServiceNow">ServiceNow</a>&nbsp;|
<a href="Simon_Property_Group" title="Simon Property Group">Simon Property Group</a>&nbsp;|
<a href="Southern_Company" title="Southern Company">Southern Company</a>&nbsp;|
<a href="Starbucks" title="Starbucks">Starbucks</a>&nbsp;|
<a href="T-Mobile_US" title="T-Mobile US">T-Mobile US</a>&nbsp;|
<a href="Target_Corporation" title="Target Corporation">Target Corporation</a>&nbsp;|
<a href="Tesla%2C_Inc." title="Tesla, Inc.">Tesla, Inc.</a>&nbsp;|
<a href="Texas_Instruments" title="Texas Instruments">Texas Instruments</a>&nbsp;|
<a href="The_Coca-Cola_Company" title="The Coca-Cola Company">The Coca-Cola Company</a>&nbsp;|
<a href="The_Home_Depot" title="The Home Depot">The Home Depot</a>&nbsp;|
<a href="The_Walt_Disney_Company" title="The Walt Disney Company">The Walt Disney Company</a>&nbsp;|
<a href="Thermo_Fisher_Scientific" title="Thermo Fisher Scientific">Thermo Fisher Scientific</a>&nbsp;|
<a href="Union_Pacific_Corporation" title="Union Pacific Corporation">Union Pacific Corporation</a>&nbsp;|
<a href="United_Parcel_Service" title="United Parcel Service">United Parcel Service</a> (Class B)&nbsp;|
<a href="UnitedHealth" title="UnitedHealth">UnitedHealth</a>&nbsp;|
<a href="U.S._Bancorp" title="U.S. Bancorp">U.S. Bancorp</a>&nbsp;|
<a href="Verizon_Communications" title="Verizon Communications">Verizon Communications</a>&nbsp;|
<a href="Visa_Inc." title="Visa Inc.">Visa Inc.</a> (Class A)&nbsp;|
<a href="Walmart" title="Walmart">Walmart</a>&nbsp;|
<a href="Wells_Fargo" title="Wells Fargo">Wells Fargo</a>
</p>
</div>
</div></div>
<div class="klappleiste mw-collapsible navileiste navigation-not-searchable center" role="navigation">
<div class="klappleiste-bild nomobile noviewer" aria-hidden="true" role="presentation"><span typeof="mw:File"></span></div>
<div class="klappleiste-kopf">Unternehmen im <i><a href="Dow_Jones_Global_Titans" title="Dow Jones Global Titans">Dow Jones Global Titans</a></i> 50 <small>(Stand: Juli 2019)</small></div>
<div class="klappleiste-inhalt mw-collapsible-content">
<div class="centered" style="display: table">
<p><a href="3M" title="3M">3M</a>&nbsp;|
<a href="Abbvie" title="Abbvie">AbbVie</a>&nbsp;|
<a href="Allianz_SE" title="Allianz SE">Allianz SE</a>&nbsp;|
<a href="Alphabet_Inc." title="Alphabet Inc.">Alphabet Inc.</a>&nbsp;|
<a href="Amazon" title="Amazon">Amazon</a>&nbsp;|
<a class="mw-selflink selflink">Amgen</a>&nbsp;|
<a href="Anheuser-Busch_InBev" title="Anheuser-Busch InBev">Anheuser-Busch InBev</a>&nbsp;|
<a href="Apple" title="Apple">Apple</a>&nbsp;|
<a href="BHP_Group" title="BHP Group">BHP</a>&nbsp;|
<a href="Boeing" title="Boeing">Boeing</a>&nbsp;|
<a href="BP" title="BP">BP</a>&nbsp;|
<a href="British_American_Tobacco" title="British American Tobacco">British American Tobacco</a>&nbsp;|
<a href="Chevron_Corporation" title="Chevron Corporation">Chevron</a>&nbsp;|
<a href="Cisco_Systems" title="Cisco Systems">Cisco</a>&nbsp;|
<a href="Citigroup" title="Citigroup">Citigroup</a>&nbsp;|
<a href="The_Coca-Cola_Company" title="The Coca-Cola Company">Coca-Cola</a>&nbsp;|
<a href="DuPont_de_Nemours" title="DuPont de Nemours">DuPont</a>&nbsp;|
<a href="ExxonMobil" title="ExxonMobil">ExxonMobil</a>&nbsp;|
<a href="Facebook" title="Facebook">Facebook</a>&nbsp;|
<a href="General_Electric" title="General Electric">General Electric</a>&nbsp;|
<a href="GlaxoSmithKline" class="mw-redirect" title="GlaxoSmithKline">GlaxoSmithKline</a>&nbsp;|
<a href="HSBC" title="HSBC">HSBC</a>&nbsp;|
<a href="IBM" title="IBM">IBM</a>&nbsp;|
<a href="Intel" title="Intel">Intel</a>&nbsp;|
<a href="Johnson_%26_Johnson" title="Johnson &amp; Johnson">Johnson &amp; Johnson</a>&nbsp;|
<a href="JPMorgan_Chase" title="JPMorgan Chase">JPMorgan Chase</a>&nbsp;|
<a href="Mastercard" title="Mastercard">Mastercard</a>&nbsp;|
<a href="McDonald%E2%80%99s" title="McDonald’s">McDonald’s</a>&nbsp;|
<a href="Merck_%26_Co." title="Merck &amp; Co.">Merck &amp; Co.</a>&nbsp;|
<a href="Microsoft" title="Microsoft">Microsoft</a>&nbsp;|
<a href="Nestl%C3%A9" title="Nestlé">Nestlé</a>&nbsp;|
<a href="Novartis" title="Novartis">Novartis</a>&nbsp;|
<a href="Nvidia" title="Nvidia">Nvidia</a>&nbsp;|
<a href="Oracle" title="Oracle">Oracle</a>&nbsp;|
<a href="PepsiCo" title="PepsiCo">PepsiCo</a>&nbsp;|
<a href="Pfizer" title="Pfizer">Pfizer</a>&nbsp;|
<a href="Philip_Morris_International" title="Philip Morris International">Philip Morris International</a>&nbsp;|
<a href="Procter_%26_Gamble" title="Procter &amp; Gamble">Procter &amp; Gamble</a>&nbsp;|
<a href="Roche_Holding" title="Roche Holding">Roche</a>&nbsp;|
<a href="Royal_Bank_of_Canada" title="Royal Bank of Canada">Royal Bank of Canada</a>&nbsp;|
<a href="Shell_plc" title="Shell plc">Royal Dutch Shell</a>&nbsp;|
<a href="Samsung_Electronics" title="Samsung Electronics">Samsung Electronics</a>&nbsp;|
<a href="Sanofi" title="Sanofi">Sanofi</a>&nbsp;|
<a href="Siemens" title="Siemens">Siemens</a>&nbsp;|
<a href="TSMC" title="TSMC">Taiwan Semiconductor</a>&nbsp;|
<a href="TotalEnergies" title="TotalEnergies">TotalEnergies</a>&nbsp;|
<a href="Toyota" title="Toyota">Toyota</a>&nbsp;|
<a href="Visa_Inc." title="Visa Inc.">Visa Inc.</a>&nbsp;|
<a href="Walmart" title="Walmart">Walmart</a>&nbsp;|
<a href="The_Walt_Disney_Company" title="The Walt Disney Company">The Walt Disney Company</a>
</p>
</div>
</div></div>
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