FDA overturns safety limits on diabetes drug
WASHINGTON (AP) — The Food and Drug Administration is lifting severe safety restrictions on the former blockbuster diabetes pill Avandia, citing recent data suggesting that the much-debated medication does not increase the risk of heart attack.
The repeal means patients will no longer have to enroll in a special registry to be eligible to receive the drug. Additionally, the drug will be available at most pharmacies, whereas it was previously limited to certain registered pharmacies. Those safety restrictions and others were put in place in 2010, severely curbing U.S. prescriptions for the GlaxoSmithKline drug.
Monday’s ruling is a belated victory for the British drugmaker, which has spent more than a half-decade defending the safety of Avandia, once the best-selling diabetes drug in the world. Sales began plummeting in 2007 after researchers first raised questions about possible links to heart attacks. After three years of debate, the FDA limited access to the drug in 2010.
But FDA regulators said Monday a more recent analysis of a key Avandia study shows that the drug’s heart risks are no greater than other diabetes drugs.
“Given these new results, our level of concern is considerably reduced,” said FDA drug center director Dr. Janet Woodcock, in a statement.
The announcement also represents a vindication of sorts for FDA leadership, including Woodcock, who only agreed to put restrictions on the pill after years of pressure from academics, safety advocates and several members of Congress.
The initial concerns about Avandia came from outside researchers who pooled thousands of reports of heart attack and stroke from dozens of unrelated studies involving Avandia. One of these so-called meta-analyses combined 42 studies and appeared to show a higher risk of heart attack among patients taking Avandia compared to other diabetes drugs.
The FDA eventually agreed to restrict use of the drug, while noting the shortcomings of the analysis that first raised the concern. FDA policy generally holds that mixing data from multiple studies can lead to misleading trends and conclusions.
That focused the agency’s attention on a study known as RECORD, the only trial to specifically compare heart attack rates in patients taking Avandia versus other standard drug treatments for diabetics.
Under instructions from the FDA, Glaxo hired Duke University to reanalyze the RECORD study, reviewing each report of heart attack or stroke at a patient-by-patient level. Duke’s findings, released last year, matched Glaxo’s initial conclusion on the study: Avandia did not appear to increase the risk of heart attack.
Last June a panel of outside experts voted to recommend easing the safety restrictions on Avandia. The FDA is not required to follow the guidance of those experts, though it often does.
Despite the ruling, GlaxoSmithKline PLC’s U.S. shares fell 61 cents, or 1.2 percent, to $52.75 in afternoon trading. Its U.S. shares have risen almost 23 percent so far this year.
Copyright 2013 The Associated Press. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.