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Amgen reports positive results from two long-term open label extension Phase 3 studies, which show injectable Repatha evolocumab safe and well-tolerated in adults with atherosclerotic cardiovascular disease; Repatha approved in US, Canada, EU, Japan

Amgen reports Q1 GAAP net income down 10% year-over-year to US$1.5B as total revenue increases 6% from a year ago to US$6.2B; Repatha evolocumab, Prolia denosumab, EVENITY romosozumab-aqqg see double-digit volume increases in Q1

Amgen breaks ground on new biomanufacturing facility in Holly Springs, North Carolina, expecting to launch operations by 2025; facility will support growing demand for medicines that treat serious illnesses such as cancer and heart disease

Amgen presents NAVIGATOR Phase 3, PATHWAY Phase 2b trials data supporting Tezspire as 'first-in-class' severe asthma treatment; data show Tezspire reduces annualized asthma exacerbation rate in patients with severe asthma irrespective of biomarker levels

FDA approves BLA 125557 for Amgen’s Blincyto injection injectable containing blinatumomab 35 mcg in one formulation; drug is available by prescription only, with no therapeutic equivalents

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