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Aegerion Receive FDA Approval For New Cholesterol Treatment

Aegerion Receive FDA Approval For New Cholesterol Treatment

Aegerion Pharmaceuticals has received FDA approval for their new cholesterol drug Juxtapid. The drug was designed specifically to lower cholesterol levels for those with a rare genetics condition known as homozygous familial hypercholesterolemia (HoFH).

Those with HoFH are incapable of clearing cholesterol from the body by normal means, which can cause fatty buildups under the skin and severely increased heart attack risk. Thus far it is unclear how many people actually suffer from the condition, raising questions about the costly drug's marketability.

Nicholas Bishop, an analyst at Cowen & Co. attempted to quell investor fears in an official statement noting:

"To better understand lomitapide's addressable market size, we conducted a survey of 9 LDL- apheresis center physicians and 18 other lipidologists. Results suggest there may be 2,400 diagnosed functional HoFH patients in the U.S. (under a restrictive label scenario) or as many as 4,000+ patients (under a more liberal label). We believe sell-side expectations vary from 300-3,000 patients."

by RTT Staff Writer

For comments and feedback: editorial@rttnews.com

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