Final results from landmark DYNAGITO® trial published in The Lancet Respiratory Medicine[1]
Results enhance existing evidence base showing Spiolto® Respimat® improves symptom reduction and quality of life over Spiriva® Respimat®[2,3,4,5,6]
For media excluding the United States of America, Canada and the United Kingdom
Final results from landmark DYNAGITO® trial published in The Lancet Respiratory Medicine
COPD is a progressive, yet treatable condition that significantly impacts patients’ lives, restricting their daily activities from early on in the disease.[8,9,10] COPD exacerbations, or flare-ups, are sudden episodes of increased breathlessness, cough and mucus production that can last for several days or even weeks.[11] These episodes can be seriously disabling, resulting in a need for urgent medical care, including hospitalisation, and sometimes lead to death.[11]
Further DYNAGITO® data demonstrated that tiotropium/olodaterol was associated with fewer moderate-to-severe exacerbations that needed intervention with a systemic corticosteroid, with or without antibiotics, compared with tiotropium:[1*]
A 20% lower rate of moderate-to-severe exacerbations that required treatment with a systemic corticosteroid (p=0.0068).[1*]
A 9% lower rate of exacerbations where the use of both a systemic corticosteroid and antibiotics were needed (p=0.0447).[1*]
No difference was observed in the rate of exacerbations that required treatment with antibiotics only (p=0.2062).[1*]
No new side effects or safety concerns were identified in the DYNAGITO® study.[1] These data also show that tiotropium/olodaterol has a similar safety profile to tiotropium.[1]
Reducing symptoms and the future risk of exacerbations are key treatment goals for COPD.[7] According to the international GOLD† 2018 Strategy recommendations, LAMA/LABA treatments such as tiotropium/olodaterol play a central role in the management of COPD and help to achieve these treatment goals.[7]
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For references and notes to editors, please visit: http://www.boehringer-ingelheim.com/press-release/results-landmark-dynagito-trial
* The pre-specified significance level of p<0.01 for the primary endpoint of DYNAGITO® was not met
† Global Initiative for Chronic Obstructive Lung Disease
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