INGELHEIM, Germany-Tuesday, May 23rd 2017 [ ME NewsWire ]
Adding tiotropium Respimat® improved lung function and asthma symptom control in children and adolescents,* regardless of their type of allergic asthma, compared to placebo1,2
The addition of tiotropium Respimat® improved airflow obstruction in adults with symptomatic asthma, independent of body mass index (BMI) compared to placebo3
In all analyses, people experiencing uncontrolled asthma symptoms saw improvements in their breathing by adding tiotropium Respimat® to an ICS or combination ICS/LABA1,2,3
(BUSINESS WIRE) -- Boehringer Ingelheim today announced new analyses that provide further evidence that adding tiotropium Respimat® (Spiriva® Respimat®) improved breathing across diverse patient populations who experience uncontrolled asthma symptoms despite the use of another daily maintenance therapy in the Phase III clinical development program. These data analyses were presented today at the American Thoracic Society International (ATS) Conference in Washington, D.C., USA.
“These new analyses add to the wealth of evidence from the large-scale UniTinA-asthma® clinical trial programme to show tiotropium Respimat® is effective in a broad range of patients with symptomatic asthma, including those with allergies or a high BMI, which may make their symptoms more difficult to manage,” said Jennifer Haddon, Global Medical Advisor Respiratory at Boehringer Ingelheim. “Of those people already on asthma treatment, almost half still experience symptoms, highlighting the need for better management. These data underline the commitment of Boehringer Ingelheim to advancing our understanding of which patients may benefit most from our medicines.”
People with allergic asthma – the most common form of the condition – can experience inflammation and a tightening of the airways when exposed to common allergens. These patients may need other options that complement their existing therapy.
For further information, please see the press release distributed by Boehringer Ingelheim US.
* Note: Spiriva® Respimat® is currently NOT APPROVED for use in children and adolescents under 18 years of age in the EU and a number of other countries. Spiriva ® Respimat® has been approved for use in asthma in over 75 countries, including in the EU, U.S. and Japan. The label and doses vary by country. Please refer to the local product information.
About Asthma
Asthma is one of the most common conditions in childhood.4 There are fewer treatment options in paediatric asthma than in adult asthma.5
Asthma is not conquered. Almost 1 in 2 patients remain symptomatic despite their current maintenance therapies (usually ICS/LABA).6, 7, 8 These symptoms have a detrimental effect on their work, education, sleep, social life and relationships.9 Additionally, symptoms increase their risk of potentially fatal asthma attacks in the next few weeks by up to six times.10
For more information please see the latest infographic.
Intended audiences:
This press release is issued from our Corporate Headquarters in Ingelheim, Germany and is intended to provide information about our global business. Please be aware that information relating to the approval status and labels of approved products may vary from country to country, and a country-specific press release on this topic may have been issued in the countries where we do business.
For references and notes to editors, please visit:
http://www.boehringer-ingelheim.com/press-release/spiriva-respimat-improves-breathing-in-asthma
Contacts
Boehringer Ingelheim
Corporate Communications
Media + PR
Meike Bausinger
Phone: +49 6132 77 182085
Mobile: +49 151 44061760
Fax: +49 6132 77 6601
Email: press@boehringer-ingelheim.com
More information
www.boehringer-ingelheim.com
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