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FDA Won't Approve MK-0653C, New Lipitor-Containing Combo Cholesterol Drug, For Now

Mk0653c Cholesterol

By LINDA A. JOHNSON   03/ 5/12 04:58 PM ET  AP

TRENTON, N.J. -- Federal regulators have rejected Merck & Co.'s new combination cholesterol drug, which includes a generic version of the mega-blockbuster Lipitor – at least for now.

It's unclear how long the ruling, announced Monday, might delay approval of the drug, as the Food and Drug Administration is requiring additional study data on the compound. It combines generic Lipitor, the top-selling drug of all time, with Merck's cholesterol medicine Zetia.

Approval could boost Merck's sagging cholesterol franchise by essentially replacing its existing combo pill, Vytorin, with one likely to be seen as more powerful. Vytorin sales have been dwindling for a few years due to concerns about how well it works, and now Merck has to contend with patients possibly defecting to the generic versions of Pfizer Inc.'s Lipitor that came on the market at the end of November.

Merck said Monday that company officials will talk with the FDA to determine the next steps, adding that some new data expected later this year may address the FDA's concerns.

Wall Street seemed unfazed by the news, perhaps because the FDA increasingly asks for additional data before approving many new drugs. In morning trading, Merck shares were up 38 cents at $38.31.

The experimental drug, still known only as MK-0653C, contains medicines that fight high cholesterol in two different ways to reduce risk of heart attack and stroke.

Lipitor, known chemically as atorvastatin, is part of the widely used class of drugs called statins that reduce the amount of cholesterol naturally produced in the liver.

Zetia, on the other hand, reduces the amount of cholesterol absorbed from the food the patient eats.

Vytorin includes Zetia and an older statin, Merck's Zocor, also called simvastatin.

Sales of Vytorin and Zetia both were hurt when Merck, under pressure from a congressional probe, in early 2008 finally released unfavorable results from a study it had hoped would bolster Vytorin sales. Instead, it showed that Vytorin was no better at reducing plaque buildup in neck arteries than just Zocor, which had been available as a cheap generic since 2006. Zetia, also known as ezetimibe, is protected by patent in the U.S. until 2017.

Lipitor, which had peak sales of around $13 billion, is a more powerful statin then Zocor. That could mean that if the new combination drug is approved, it would be tried by at least some patients who have not been able to get their cholesterol numbers to their goal with Vytorin or other treatments.

Meanwhile, last year Lipitor maker Pfizer sued, alleging Merck's application for the FDA to approve the Zetia-atorvastatin combination infringed on a Pfizer patent covering atorvastatin.

A Merck spokeswoman said Monday that the lawsuit "has the potential for holding up FDA approval of the Merck product until" the first quarter of 2014.

___

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TRENTON, N.J. -- Federal regulators have rejected Merck & Co.'s new combination cholesterol drug, which includes a generic version of the mega-blockbuster Lipitor – at least for now. It's uncle...
TRENTON, N.J. -- Federal regulators have rejected Merck & Co.'s new combination cholesterol drug, which includes a generic version of the mega-blockbuster Lipitor – at least for now. It's uncle...
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08:37 PM on 03/08/2012
Why so glum? I'm sure it will be approved once it is resubmitted.

Hate to say this but... anyone seen Dateline NBC Hansen Expose of FDA Drug Testing? We gotta stop thinking that doctors are on our side. I have never, and will never take any type of medication on a prolong basis, esp. birth control. It is a woman's right to choose, I choose not to have complications because of it.
03:13 PM on 03/06/2012
Lipitor the top selling drug of all time? Bitch please. Marijuana outsells lipitor's entire existence in a single day.
02:13 PM on 03/06/2012
Cholesterol, per se, has nothing to do with heart disease. It's not even LDL per se, but small LDL that does all the damage. And the way people get way too much small LDL is by eating too much refined carbohydrates and sugar.

Although I certainly understand why drug companies don't keep up with the science (profit), it would be nice if the medical community and Huffington Post stayed current.
02:49 PM on 03/08/2012
Yes, and we should also mention that the tests for determining small LDL from large LDL requires a very expensive, as in millions $'s, machine normally used for experiments with quantum mechanics. I.E. you won't have your LDL tested to know what your actual numbers are!
It's ALL marketing and profit people, with no data to prove extension of your lives, with some drugs, such as Crestor proven to be highly dangerous unless great precautions are taken.
07:39 PM on 03/08/2012
I've read that LDL size can be tested by private labs for about $100. If that's true then it should be a standard test. But a good work around is that high triglycerides (a part of the standard testing) strongly correlate to small LDL. So at least we can get a good idea.
12:48 PM on 03/06/2012
Yesterday an article about the cost of producing a new drug . Average 100 to 200 million dollars to 1 billion on other types . Just one of the additions to the cost of health care .
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Will Vazquez
11:52 AM on 03/06/2012
who is watching the F.D.A . the public needs to know what there doing .and also be able to make there own decision on drugs they want to take ....