New study finds little difference in cardiac risk for GlaxoSmithKline's Avandia and Takeda's Actos

25 August 2010

In contrast to previous reports, the risks of the composite endpoint of heart attack, heart failure, both, or death were the same - about 4% - for patients taking the diabetes drugs Avandia (rosiglitazone) from UK pharma giant GlaxoSmithKline (GSK: L) or Actos (pioglitazone) from Takeda (4502.TO), Japan's largest drugmaker, according to a study published in the American Heart Association journal Circulation: Cardiovascular Quality and Outcomes.

This is clearly welcome news for GSK, whose Avandia - which has been the subject of severe adverse comment about its side effects for the past few years (and has seen its sales significantly reduced) - missed being taken off the US market after a Food and Drug Administration advisory panel voted in support of the drug (The Pharma Letter July 15). Avandia's future is also under review by the European Medicines Agency (EMEA).

Actos gained from negative safety profile of Avandia

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