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Do you want to link to this Amgen Site outside the UK and leave Amgen.co.uk? Our research drives us to understand the disease in the context of the patient's life – not just their cancer journey – so they can take control of their lives. About IMLYGIC® (talimogene laherparepvec) IMLYGIC is a genetically modified herpes simplex type 1 virus that is injected directly into tumors. Please note, this page is intended for UK healthcare professionals. An outbreak of disease or similar public health threat, such as COVID-19, and the public and governmental effort to mitigate against the spread of such disease, could have a significant adverse effect on the supply of materials for our manufacturing activities, the distribution of our products, the commercialization of our product candidates, and our clinical trial operations, and any such events may have a material adverse effect on our product development, product sales, business and results of operations.
Authorized Products, Next: Also, we or others could identify safety, side effects or manufacturing problems with our products, including our devices, after they are on the market. Pre-medicate with dexamethasone to reduce the incidence and severity of infusion reactions. Fatal or serious cases of hemorrhage have been reported. The discovery of significant problems with a product similar to one of our products that implicate an entire class of products could have a material adverse effect on sales of the affected products and on our business and results of operations. Updated results from a Phase 1 dose escalation study of AMG 330, a BiTE® (bispecific T cell engager) molecule, in acute myeloid leukemia will be featured in an oral presentation. We are consolidating our U.S.-based Research presence primarily in Thousand Oaks and San Francisco. Please see www.Imlygic.com for full Prescribing Information, including Medication Guide. Even when clinical trials are successful, regulatory authorities may question the sufficiency for approval of the trial endpoints we have selected.

Do you want to link to this External Site and leave Amgen.co.uk? Our business may be impacted by government investigations, litigation and product liability claims. Further, some raw materials, medical devices and component parts for our products are supplied by sole third-party suppliers. Reduce or withhold dose as appropriate. Monitor platelet counts frequently during treatment. The safety of reinitiating KYPROLIS is not known. Inform patients of the risk and of symptoms and seek immediate medical attention if they occur. CONTACT: Amgen, Thousand Oaks Trish Rowland, 805-447-5631 (media) Arvind Sood, 805-447-1060 (investors), View original content to download multimedia:http://www.prnewswire.com/news-releases/amgen-showcases-oncology-pipeline-at-asco-2020-301058857.html. KYPROLIS can cause increased serum transaminases. If this drug is used during pregnancy, or if pregnancy occurs while taking this drug, the patient should be apprised of the potential hazard to the fetus. Biotechnology has brought about the discovery and development of a new generation of human therapeutics. }); Clinical Trial Transparency, Data Sharing and Disclosure Practices, Adverse Event and Product Complaint Reporting, Corporate Responsibility Strategy & Governance, Our Approach to Pricing, Access and Affordability, Reimbursement Support Services and Financial Assistance Programs. Such product candidates are not approved by the U.S. Food and Drug Administration, and no conclusions can or should be drawn regarding the safety or effectiveness of the product candidates. Amgen Pipeline Amgen has developed a robust and differentiated pipeline, leveraging state-of-the-art science to create medicines for serious illnesses. In addition, sales of our products are affected by pricing pressure, political and public scrutiny and reimbursement policies imposed by third-party payers, including governments, private insurance plans and managed care providers and may be affected by regulatory, clinical and guideline developments and domestic and international trends toward managed care and healthcare cost containment. Discontinue if diagnosis is suspected. IMLYGIC is the first and only oncolytic viral therapy approved by the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA), and other regulatory authorities, based on therapeutic benefit demonstrated in a pivotal Phase 3 study. Thromboprophylaxis is recommended for patients being treated with the combination of KYPROLIS with dexamethasone or with lenalidomide plus dexamethasone. Amgen has developed a collection of online resources available to help you learn more about areas of interest. KYPROLIS is approved in the U.S. for the following: KYPROLIS is also approved in Algeria, Argentina, Australia, Bahrain, Belarus, Brazil, Canada, Chile, Colombia, Ecuador, Egypt, European Union, Hong Kong, India, Israel, Japan, Jordan, Kuwait, Lebanon, Macao, Malaysia, Mexico, Morocco, New Zealand, Oman, Peru, Philippines, Qatar, Russia, Saudi Arabia, Singapore, S. Korea, Switzerland, Taiwan, Thailand, Turkey and United Arab Emirates. Cases of thrombotic microangiopathy, including thrombotic thrombocytopenic purpura/hemolytic uremic syndrome (TTP/HUS), including fatal outcome have occurred. The products are not approved for the investigational use(s) discussed in this news release, and no conclusions can or should be drawn regarding the safety or effectiveness of the products for these uses. KYPROLIS causes thrombocytopenia with recovery to baseline platelet count usually by the start of the next cycle. Discovery or identification of new product candidates or development of new indications for existing products cannot be guaranteed and movement from concept to product is uncertain; consequently, there can be no guarantee that any particular product candidate or development of a new indication for an existing product will be successful and become a commercial product. Withhold KYPROLIS for Grade 3 or 4 cardiac adverse events until recovery, and consider whether to restart at 1 dose level reduction based on a benefit/risk assessment. New onset or worsening of pre-existing cardiac failure (e.g., congestive heart failure, pulmonary edema, decreased ejection fraction), restrictive cardiomyopathy, myocardial ischemia, and myocardial infarction including fatalities have occurred following administration of KYPROLIS.

About Amgen Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. Information regarding presentation times, webcast availability and webcast links are noted on Amgen's Investor Relations Events Calendar.

Forward-Looking Statements This news release contains forward-looking statements that are based on the current expectations and beliefs of Amgen. No forward-looking statement can be guaranteed and actual results may differ materially from those we project. Learn More . To learn more about Amgen's innovative pipeline with diverse modalities and genetically validated targets, please visit www.AmgenOncology.com. Amgen is a values-based company, deeply rooted in science and innovation to transform new ideas and discoveries into medicines for patients with serious illnesses.

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