The highly-anticipated decision introduces a new option for patients at risk for heart disease. But questions remain about the drug's price estimated by one analyst at about USD 3,750 per year outside the US and its ability to reduce heart attack and death in the long term.
The European Commission cleared Repatha for patients with dangerously high cholesterol levels, including those with inherited conditions that drive up levels of the wax-like substance.
The injectable drug should be used by patients who cannot control their cholesterol with older statin drugs, or cannot tolerate them due to side effects, the group said.
The US Food and Drug Administration is scheduled to make a decision on a similar drug from Sanofi and Regeneron Pharmaceuticals this Friday. The FDA's target date for reviewing Amgen's drug is August 27.
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Both drugs lower low-density lipoprotein, or LDL, cholesterol more powerfully and in a different ways than currently available drugs.
They block a substance called PCSK9, which interferes with the liver's ability to remove cholesterol from the blood. Adding the new drugs to older statins reduces LDL cholesterol by about 40 per cent to 60 per cent.
"Our prices are managed with consideration to competition, the local pricing and reimbursement environment and patient-cost sharing obligation, which vary considerably by country," said Kristen Davis, in a statement.
Repatha and other PCSK9 drugs are expected to grow into blockbuster products, though prescribing may be limited at first by strict reimbursement in Europe and the US.