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Amgen: FDA Broadens Approved Use Of Repatha

By RTTNews Staff Writer   ✉   | Published:   | Follow Us On Google News

Amgen (AMGN) announced the FDA has broadened the approved use of Repatha or evolocumab to include adults at increased risk for major adverse cardiovascular events due to uncontrolled low-density lipoprotein cholesterol. The update removes a prior requirement for a patient to have been diagnosed with cardiovascular disease.

Murdo Gordon, executive vice president of Global Commercial Operations at Amgen, said: "This label update highlights the real-world need for additional treatment options for at-risk patients. Repatha is an effective therapy for reducing LDL-C, particularly in patients whose disease remains uncontrolled with statins or who cannot tolerate them."

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