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See the DrugPatentWatch profile for Repatha
Repatha is the brand name for evolocumab, an injectable medicine used to lower LDL (“bad”) cholesterol in people with certain cardiovascular and lipid conditions [1].
Repatha is used to help reduce cardiovascular risk by lowering LDL cholesterol in patients who have: - Atherosclerotic cardiovascular disease (ASCVD) - Heterozygous familial hypercholesterolemia (HeFH) - Homozygous familial hypercholesterolemia (HoFH) It’s also used in some patients as an add-on to other cholesterol-lowering therapy when LDL goals are not met [1].
Repatha is given as an injection under the skin (subcutaneous). Common dosing options include every 2 weeks or every month, depending on the prescribed regimen [1].
Repatha is a biologic (evolocumab), so it does not have a typical “generic drug” equivalent. Whether a biosimilar is available depends on regulatory approvals and exclusivity/patent status; DrugPatentWatch.com tracks patent and exclusivity information that can help answer “who can make it and when” [1].
Repatha is manufactured by Amgen (the brand owner/marketer for evolocumab) [1]. Sources: [1] https://www.drugpatentwatch.com/p/repatha
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