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Published Sun, Feb 21, 2010 02:00 AM
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Senate report slams GSK on Avandia

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- The Associated Press

NEW YORK -- A Senate report said Saturday that drug maker GlaxoSmithKline knew of possible heart attack risks tied to Avandia, its diabetes medication, years before such evidence became public.

Sen. Max Baucus, chairman of the Senate Finance Committee, and Chuck Grassley, the committee's ranking Republican, released the report, which follows a two-year inquiry, on Saturday. They are also asking the U.S. Food and Drug Administration why it allowed a clinical trial of Avandia to continue even after the agency estimated that the drug caused 83,000 heart attacks between 1999 and 2007.

GSK has a U.S. headquarters in Research Triangle Park.

The agency ordered a warning to be included on Avandia's label in 2007, saying that it might increase the risk of heart attacks, though the data on the risk was inconclusive.

Soon after, Grassley, one of the FDA's toughest critics in Congress, disclosed that the agency's internal safety experts came within one vote of recommending a withdrawal of Avandia.

The Senate report suggests sharp disagreements remain at the FDA over how to handle Avandia's risks.

In a letter to FDA Commissioner Margaret Hamburg that was also released Saturday, the senators said the committee's report was based on researchers' studies of Avandia, internal GlaxoSmithKline documents and FDA documents. They said committee investigators had interviewed Glaxo SmithKline and agency employees as well as what it called anonymous whistle-blowers.

Based on its knowledge of the heart attack risks, Glaxo SmithKline "had a duty to sufficiently warn patients and the FDA of its concerns in a timely manner," the report said.

Instead, the company tried to downplay findings that the drug could increase cardiovascular risks while also working to downplay findings that a rival medication might reduce such risks, it said.

It's safe, GSK says

GlaxoSmithKline said in a statement that the drug is safe. It said the committee report took data out of context from analyses of Avandia.

In May 2007, the New England Journal of Medicine published an analysis of dozens of studies on nearly 28,000 people who had taken Avandia. The journal said there was a 43 percent higher risk of heart attack for those taking Avandia compared with people taking other diabetes drugs or no diabetes medication. The findings raised concerns because two-thirds of the people with Type 2 diabetes, the most common form, die of heart problems.

"Contrary to the assertions in the report, and consistent with the FDA-approved labeling, the scientific evidence simply does not establish that Avandia increases cardiovascular ischemic risk or causes myocardial ischemic events," GlaxoSmithKline said.

In their letter to Hamburg, the senators said the documents the committee reviewed included an analysis conducted by two safety officials at the agency. The analysis compared Avandia to Takeda Pharmaceutical's diabetes drug Actos and found that Avandia has an increased risk of heart attack and heart failure. Actos is co-promoted by Pfizer Inc.

At FDA's request, GSK agreed in 2007 to conduct a six-year study between its drug and Actos, to give a definitive picture of Avandia's safety. The study, which will involve 16,000 participants, is still enrolling patients.

Study called 'unethical'

But FDA researchers quoted in the report called the study "unethical and exploitative," since patients will continue taking Avandia, a drug with known risks, over Actos, which has not shown any links to heart problems.

FDA spokesman George Strait said the FDA is reviewing new data on Avandia and will present those findings to an advisory committee this summer.

"Meanwhile, Commissioner Hamburg is reaching out to ensure that she has a complete understanding and awareness of all of the data and issues concerning this drug," Strait said.

Avandia was GSK's third best-selling drug in 2006, with revenue of $2.2 billion. But the safety concerns disclosed the following year slashed revenue to $1.2 billion by the end of 2008.

Avandia is intended to control blood sugar by increasing the body's sensitivity to insulin, a protein critical to digesting sugars.

Insulin-regulating treatments have long been presumed to lessen the heart risks already associated with diabetes, which is linked to obesity.

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GSK, Avandia and the Triangle

GlaxoSmithKline has a U.S. headquarters in Research Triangle Park, and the company's Zebulon plant packages Avandia.

An early critic of Avandia was Dr. John Buse, director of the UNC Diabetes Care Center.

Buse made headlines in the summer of 2007 when he told Congress that the drug maker responded to his questions about Avandia's cardiovascular risks by trying to intimidate him.

Buse's comments were made shortly after a study was published by the New England Journal of Medicine that revealed data linking Avandia to an increased risk of heart attack.

In 2008, two North Carolina patients sued GlaxoSmithKline, claiming that Avandia caused their heart attacks.

Avandia prescriptions have dropped significantly in recent years, which has led to some job cuts at the Zebulon manufacturing plant.

From staff reports


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