USFDA approves Praluent- breakthrough drug to lower bad cholesterol
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FDA has given its nod to a breakthrough cholesterol drug from Sanofi and Regeneron Pharmaceuticals Inc. that offers an important new option for patients at high risk of heart disease
The Food and Drug Administration has given a green signal to introduce new cholesterol drug-considered to be a breakthrough for lowering the risk of heart disease. The development comes after a gap of 20 years, since any new such medicine was prescribed.
The USFDA approved Praluent (alirocumab) injection, the first cholesterol-lowering treatment approved in a new class of drugs known as proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors.
Praluent is approved for use in addition to diet and maximally tolerated statin therapy in adult patients with heterozygous familial hypercholesterolemia (HeFH) or patients with clinical atherosclerotic cardiovascular disease such as heart attacks or strokes, who require additional lowering of LDL cholesterol.
The Food and Drug Administration has given a green signal to introduce new cholesterol drug-considered to be a breakthrough for lowering the risk of heart disease. The development comes after a gap of 20 years, since any new such medicine was prescribed.
The USFDA approved Praluent (alirocumab) injection, the first cholesterol-lowering treatment approved in a new class of drugs known as proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors.
Praluent is approved for use in addition to diet and maximally tolerated statin therapy in adult patients with heterozygous familial hypercholesterolemia (HeFH) or patients with clinical atherosclerotic cardiovascular disease such as heart attacks or strokes, who require additional lowering of LDL cholesterol.
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