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Diabetes Drug Should Stay Despite Heart Risks, U.S. Advisers Say
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Page: << Prev | 1 | 2 | 3 | 4 | 5 | Next >> Dr. Sidney Wolfe, director of Public Citizen's Health Research Group, who has previously spoken out against Avandia, was among the speakers at the hearing. "Does the overall risk-benefit profile of Avandia support its continued marketing in the United States? The answer is clearly no," he said in a prepared statement.
According to Wolfe's prepared testimony, FDA adverse-reaction reports filed since Avandia hit the market in 1999 have shown the drug had a 15.2 times higher adjusted rate of heart failure than did the older diabetes drug Glucotrol. The adjusted rate of liver toxicity with Avandia was 9.5 times higher, and 14.8 times higher for liver failure, he said.
"There is no evidence of any uniquely beneficial clinical outcome for Avandia and growing evidence of unique risks in multiple organ systems," Wolfe said. "If Avandia were up for approval today, based on what is now known, it would be summarily rejected. There should not be a double standard for removing it from the market."
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For its part, Avandia's maker, GlaxoSmithKline, insisted before the meeting that the drug does not increase the risk of heart attack. "We don't believe that a warning about heart attack should be on the label," said Dr. Andy Zambanini, director of clinical development at GlaxoSmithKline.
"Avandia is one of the most studied medicines in the diabetes field," Zambanini said. "We have looked at all the available data both from short-term trials, long-term trials and real-world data, in terms of epidemiology. There is really no evidence of an increase in cardiovascular death with Avandia. And when you look at Avandia and compare it with all the other similar agents, there really is no difference in heart attack risk."
One of the studies that GlaxoSmithKline is relying on to make its case is the RECORD (Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycemia in Diabetes) trial. The study, sponsored by Glaxo, was specifically designed to determine the risks for heart attack from Avandia.
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Copyright © 2007 ScoutNews, LLC. All rights reserved.
Last updated 7/31/2007
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SOURCES: July 30, 2007, U.S. Food and Drug Administration teleconference with Robert Meyer, M.D., director, FDA's Office of Evaluation II, Center for Drug Evaluation and Research; and
Clifford Rosen, M.D., acting committee chairman, Maine Center for Osteoporosis, St. Joseph Hospital, Bangor, Maine; and Gerald Dal Pan, M.D., director of the FDA's Office of Surveillance and Epidemiology;
Larry Deeb, M.D., president, medicine and science, American Diabetes Association, Alexandria, Va.; Andy Zambanini, M.D., director, clinical development, GlaxoSmithKline; July 30, 2007, prepared statement, Sidney Wolfe, M.D., director of Public Citizen's Health Research Group, Washington, D.C.; July 30, 2007, prepared statement, GlaxoSmithKline
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