AUSTRI study of Advair Diskus, (LABA, salmeterol and fluticasone propionate) in asthma published in New England Journal of Medicine- GlaxoSmithKline
GlaxoSmithKline announced publication of results from the safety study, AUSTRI (SAS115359) in the New England Journal of Medicine (NEJM). The study, which reported results in October, compared Advair Diskus (LABA, salmeterol and fluticasone propionate) to fluticasone propionate (FP) monotherapy, to assess the safety profiles of each medicine when used to treat adolescent and adult patients with asthma.
This was assessed by the composite endpoint of serious asthma-related events (deaths, intubations or hospitalisations) and showed that Advair had a safety profile comparable to FP, including no asthma-related deaths in either arm. These results are being simultaneously presented at the American Academy of Asthma, Allergy and Immunology Congress in Los Angeles, California.