THOUSAND OAKS, Calif.?and?BRUSSELS,?Oct. 17, 2019?/PRNewswire/ --?Amgen?(NASDAQ:AMGN) and UCB (Euronext Brussels: UCB) today announced that following a re-examination procedure, the?Committee for Medicinal Products for Human Use?(CHMP) of the?European Medicines Agency?(EMA) has adopted a positive opinion recommending Marketing Authorization for EVENITY^??(romosozumab) for the treatment of severe osteoporosis in postmenopausal women at high risk of fracture and with no history of myocardial infarction or stroke. EVENITY is a novel bone-builder with a dual effect that increases bone formation and to a lesser extent reduces bone resorption (or bone loss). "After a fracture, postmenopausal women with osteoporosis are five times more likely to fracture in the subsequent year,¹?and these fractures can be life-changing," said?David M. Reese, M.D., executive vice president of Research and Development at?Amgen. "We are pleased by the Committee's opinion because we believe EVENITY is an important therapeutic development for osteoporosis, and we look forward to the?European Commission's?decision later this year." The CHMP's recommendation will now be reviewed by the?European Commission?(EC), which has the authority to approve medicines for use throughout the?European Union. A?European Commission?decision is expected by year-end 2019. "Post-menopausal osteoporosis and fragility fractures are significant women's health issues that are far too often overlooked, with evidence suggesting that an estimated 77 percent of women aged 67 or older remain undiagnosed and untreated in the first 6 months after a fracture.²?This is why new treatment options are so important," said Dr.?Pascale Richetta, head of bone and executive vice president, UCB. "We believe that the Committee's positive opinion is an important step forward to help improve the lives of postmenopausal women with severe osteoporosis who are at high risk of fragility fractures." EVENITY is approved in U.S. for the treatment of osteoporosis in postmenopausal women at high risk for fracture.³?EVENITY is also approved in?Japan?and?South Korea?for the treatment of osteoporosis for women and men at high risk for fracture, in?Canada?for the treatment of osteoporosis for postmenopausal women at high risk for fracture, and in?Australia?for the treatment of osteoporosis in postmenopausal women at high risk of fracture and as a treatment to increase bone mass in men with osteoporosis at high risk of fracture.?^4-7 About EVENITY^??(romosozumab) EVENITY is a bone-forming monoclonal antibody. It is designed to work by inhibiting the activity of sclerostin, which simultaneously results in increased bone formation and to a lesser extent decreased bone resorption. The EVENITY development program includes 19 clinical studies that enrolled approximately 14,000 patients. EVENITY has been studied for its potential to reduce the risk of fractures in an extensive global Phase 3 program that included two large fracture trials comparing EVENITY to either placebo or active comparator in nearly 11,000 postmenopausal women with osteoporosis.?Amgen?and UCB are co-developing EVENITY. About the Pivotal EVENITY Clinical Trials FRAME (Fracture study in postmenopausal women with osteoporosis) is a randomized, double-blind, placebo-controlled study that evaluated 7,180 postmenopausal women with osteoporosis at risk for fracture. The study evaluated the effectiveness of EVENITY treatment (210 mg, administered monthly), compared with placebo, in reducing the risk of new vertebral fractures through 12 months. The study also evaluated the effectiveness of treating with EVENITY for 12 months followed by denosumab for 12 months, compared with placebo followed by denosumab, in reducing the risk of new vertebral fractures through 24 months. ARCH (Active-controlled fracture study in postmenopausal women with osteoporosis at?high risk of fracture) is a randomized, double-blind, alendronate-controlled study of EVENITY in 4,093 postmenopausal women with osteoporosis and previous fracture history. This event-driven study evaluated 12 months of EVENITY treatment (210 mg, administered monthly), followed by at least 12 months of alendronate treatment (70 mg), compared with alendronate treatment alone, to assess its efficacy in reducing the risk of clinical fracture (non-vertebral fracture and symptomatic vertebral fracture) through the primary analysis period and the incidence of new vertebral fracture at 24 months. BRIDGE (Placebo-controlled study evaluating the efficacy and?safety of romosozumab in treating?men with osteoporosis) is a randomized, double-blind, placebo-controlled study of 245 men aged 55-90 years with osteoporosis and a history of fragility fracture (excluding hip fracture) or vertebral fracture. The study evaluated the effectiveness of EVENITY treatment (210 mg, administered monthly) for 12 months, compared with placebo, in increasing bone mineral density (BMD) at the lumbar spine and the effect on BMD at the femoral neck and total hip. About Osteoporosis-Related Fractures Worldwide, one in three women and one in five men, over the age of 50, will suffer a fragility fracture due to osteoporosis and with an aging population these numbers will rise.⁸?Yet despite this, there is a large gap in the management and treatment of osteoporosis, especially in the post-fracture setting, with an estimated four out of five patients remaining undiagnosed and untreated after a fracture.⁹?Without proper care or access to effective intervention options, they remain at risk of painful and disabling fractures in the future. Important U.S. Product Information EVENITY^??is indicated for the treatment of osteoporosis in postmenopausal women at high risk for fracture, defined as a history of osteoporotic fracture, or multiple risk factors for fracture; or patients who have failed or are intolerant to other available osteoporosis therapy. The anabolic effect of EVENITY wanes after 12 monthly doses of therapy. Therefore, the duration of EVENITY use should be limited to 12 monthly doses. If osteoporosis therapy remains warranted, continued therapy with an anti-resorptive agent should be considered. Important U.S. Safety Information POTENTIAL RISK OF MYOCARDIAL INFARCTION, STROKE AND CARDIOVASCULAR DEATH EVENITY^??may increase the risk of myocardial infarction, stroke and cardiovascular death. EVENITY^??should not be initiated in patients who have had a myocardial infarction or stroke within the preceding year. Consider whether the benefits outweigh the risks in patients with other cardiovascular risk factors. Monitor for signs and symptoms of myocardial infarction and stroke and instruct patients to seek prompt medical attention if symptoms occur. If a patient experiences a myocardial infarction or stroke during therapy, EVENITY^??should be discontinued. In a randomized controlled trial in postmenopausal women, there was a higher rate of major adverse cardiac events (MACE), a composite endpoint of cardiovascular death, nonfatal myocardial infarction and nonfatal stroke, in patients treated with EVENITY^TM?compared to those treated with alendronate. Contraindications:?EVENITY^??is contraindicated in patients with hypocalcemia. Pre-existing hypocalcemia must be corrected prior to initiating therapy with EVENITY^?. EVENITY^??is contraindicated in patients with a history of systemic hypersensitivity to romosozumab or to any component of the product formulation. Reactions have included angioedema, erythema multiforme and urticaria. Hypersensitivity:?Hypersensitivity reactions, including angioedema, erythema multiforme, dermatitis, rash and urticaria have occurred in EVENITY^TM-treated patients. If an anaphylactic or other clinically significant allergic reaction occurs, initiate appropriate therapy and discontinue further use of EVENITY^?. Hypocalcemia:?Hypocalcemia has occurred in patients receiving EVENITY^?. Correct hypocalcemia prior to initiating EVENITY^?. Monitor patients for signs and symptoms of hypocalcemia, particularly in patients with severe renal impairment or receiving dialysis. Adequately supplement patients with calcium and vitamin D while on EVENITY^?. Osteonecrosis of the Jaw (ONJ):?ONJ, which can occur spontaneously, is generally associated with tooth extraction and/or local infection with delayed healing, and has been reported in patients receiving EVENITY^?. A routine oral exam should be performed by the prescriber prior to initiation of EVENITY^?. Concomitant administration of drugs associated with ONJ (chemotherapy, bisphosphonates, denosumab, angiogenesis inhibitors, and corticosteroids) may increase the risk of developing ONJ. Other risk factors for ONJ include cancer, radiotherapy, poor oral hygiene, pre-existing dental disease or infection, anemia and coagulopathy. For patients requiring invasive dental procedures, clinical judgment should guide the management plan of each patient. Patients who are suspected of having or who develop ONJ should receive care by a dentist or an oral surgeon. In these patients, dental surgery to treat ONJ may exacerbate the condition. Discontinuation of EVENITY^??should be considered based on benefit-risk assessment. Atypical Femoral Fractures:?Atypical low-energy or low trauma fractures of the femoral shaft have been reported in patients receiving EVENITY^?. Causality has not been established as these fractures also occur in osteoporotic patients who have not been treated. During EVENITY^??treatment, patients should be advised to report new or unusual thigh, hip or groin pain. Any patient who presents with thigh or groin pain should be evaluated to rule out an incomplete femur fracture. Interruption of EVENITY^??therapy should be considered based on benefit-risk assessment. Adverse Reactions:?The most common adverse reactions (= 5%) reported with EVENITY^??were arthralgia and headache. EVENITY^??is a humanized monoclonal antibody. As with all therapeutic proteins, there is potential for immunogenicity. Please see accompanying EVENITY^??full?Prescribing Information, including Boxed Warning and Medication Guide. About the?Amgen?and UCB Collaboration Since 2004,?Amgen?and UCB have been working together under a collaboration and license agreement to research, develop and market antibody products targeting the protein sclerostin. As part of this agreement, the two companies continue to collaborate on the development of romosozumab for the treatment of osteoporosis. This gene-to-drug project demonstrates how?Amgen?and UCB are joining forces to translate a genetic discovery into a new medicine, turning conceptual science into a reality. 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. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen?focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980,?Amgen?has grown to be the world's largest independent biotechnology company, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit?www.amgen.com?and follow us on?www.twitter.com/amgen. About UCB UCB,?Brussels, Belgium?(www.ucb.com) is a global biopharmaceutical company focused on the discovery and development of innovative medicines and solutions to transform the lives of people living with severe diseases of the immune system or of the central nervous system. With more than 7,700 people in approximately 40 countries, the company generated revenue of ? 4.2 billion in 2016. UCB is listed on Euronext Brussels (symbol: UCB). Follow us on Twitter: @UCB_news Amgen Forward-Looking Statements This news release contains forward-looking statements that are based on the current expectations and beliefs of?Amgen. All statements, other than statements of historical fact, are statements that could be deemed forward-looking statements, including any statements on the outcome, benefits and synergies of the acquisition of Otezla^??(apremilast), including anticipated Otezla sales growth and the timing of non-GAAP EPS accretion, as well as estimates of revenues, operating margins, capital expenditures, cash, other financial metrics, expected legal, arbitration, political, regulatory or clinical results or practices, customer and prescriber patterns or practices, reimbursement activities and outcomes and other such estimates and results.?Forward-looking statements involve significant risks and uncertainties, including those discussed below and more fully described in the?Securities and Exchange Commission?reports filed by?Amgen, including its most recent annual report on Form 10-K and any subsequent periodic reports on Form 10-Q and current reports on Form 8-K. Unless otherwise noted,?Amgen?is providing this information as of the date of this news release and does not undertake any obligation to update any forward-looking statements contained in this document as a result of new information, future events or otherwise. No forward-looking statement can be guaranteed and actual results may differ materially from those?Amgen?projects. 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. Further, preclinical results do not guarantee safe and effective performance of product candidates in humans. The complexity of the human body cannot be perfectly, or sometimes, even adequately modeled by computer or cell culture systems or animal models. The length of time that it takes for?Amgen?to complete clinical trials and obtain regulatory approval for product marketing has in the past varied and?Amgen?expects similar variability in the future. Even when clinical trials are successful, regulatory authorities may question the sufficiency for approval of the trial endpoints?Amgen?has selected.?Amgen?develops product candidates internally and through licensing collaborations, partnerships and joint ventures. Product candidates that are derived from relationships may be subject to disputes between the parties or may prove to be not as effective or as safe as?Amgen?may have believed at the time of entering into such relationship. Also,?Amgen?or others could identify safety, side effects or manufacturing problems with its products, including its devices, after they are on the market. Amgen's?results may be affected by its ability to successfully market both new and existing products domestically and internationally, clinical and regulatory developments involving current and future products, sales growth of recently launched products, competition from other products including biosimilars, difficulties or delays in manufacturing its products and global economic conditions. In addition, sales of?Amgen's?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. 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Further, while?Amgen?routinely obtains patents for its products and technology, the protection offered by its patents and patent applications may be challenged, invalidated or circumvented by its competitors, or?Amgen?may fail to prevail in present and future intellectual property litigation.?Amgen?performs a substantial amount of its commercial manufacturing activities at a few key facilities, including in?Puerto Rico, and also depends on third parties for a portion of its manufacturing activities, and limits on supply may constrain sales of certain of its current products and product candidate development.?Amgen?relies on collaborations with third parties for the development of some of its product candidates and for the commercialization and sales of some of its commercial products. In addition,?Amgen?competes with other companies with respect to many of its marketed products as well as for the discovery and development of new products. Further, some raw materials, medical devices and component parts for?Amgen's?products are supplied by sole third-party suppliers. Certain of?Amgen's?distributors, customers and payers have substantial purchasing leverage in their dealings with?Amgen. The discovery of significant problems with a product similar to one of?Amgen's?products that implicate an entire class of products could have a material adverse effect on sales of the affected products and on its business and results of operations.?Amgen'sefforts to acquire other companies or products and to integrate the operations of companies?Amgen?has acquired may not be successful. A breakdown, cyberattack or information security breach could compromise the confidentiality, integrity and availability of?Amgen's?systems and?Amgen's?data.?Amgen's?stock price may be volatile and may be affected by a number of events.?Amgen's?business performance could affect or limit the ability of the Amgen Board of Directors to declare a dividend or its ability to pay a dividend or repurchase its common stock.?Amgen?may not be able to access the capital and credit markets on terms that are favorable to it, or at all. The scientific information discussed in this news release related to?Amgen's?product candidates is preliminary and investigative. Such product candidates are not approved by the?European Medicines Agency, and no conclusions can or should be drawn regarding the safety or effectiveness of the product candidates. UCB Forward-Looking Statements This press release contains forward-looking statements based on current plans, estimates and beliefs of management. 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There is no guarantee that new product candidates in the pipeline will progress to product approval or that new indications for existing products will be developed and approved. Products or potential products which are the subject of partnerships, joint ventures or licensing collaborations may be subject to differences between the partners. Also, UCB or others could discover safety, side effects or manufacturing problems with its products after they are marketed. Moreover, sales may be impacted by international and domestic trends toward managed care and health care cost containment and the reimbursement policies imposed by third-party payers as well as legislation affecting biopharmaceutical pricing and reimbursement. CONTACT:?Amgen,?Thousand Oaks Jessica Akopyan, 805-447-0974 (media) Trish Hawkins, 805-447-5631 (media Arvind Sood, 805-447-1060 (investors) CONTACT: UCB, Brussels France Nivelle,?Global Communications, UCB T +32.2.559.9178,?france.nivelle@ucb.com? Laurent Schots, Media Relations, UCB T+32.2.559.92.64,?laurent.schots@ucb.com Antje Witte, Investor Relations, UCB T +32.2.559.94.14,?antje.witte@ucb.com Isabelle Ghellynck, Investor Relations, UCB T+32.2.559.9588,?isabelle.ghellynck@ucb.com? References

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