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Key results from new tiotropium studies in COPD and asthma to be presented at ERS 2012


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INGELHEIM,Germany--([ ])--New data to be presented at the Annual Congress of the European Respiratory Society (ERS 2012), in Vienna, Austria, will shed light on the current and potential future role of tiotropium, the first once-daily long-acting inhaled anticholinergic for patients with Chronic Obstructive Pulmonary Disease (COPD).

Highlights from the accepted abstracts include the first Phase III exacerbation and lung function data for Boehringer Ingelheimas and Pfizeras tiotropium in asthma. These results derive from two replicate studies evaluating the efficacy of once-daily tiotropium administered by the Respimat Soft MistTM Inhaler (SMI) in patients with severe asthma who remain symptomatic on at least ICSC/LABAD. The data are relevant since a significant proportion of patients with asthma remain symptomatic despite current treatment options and may have asthma exacerbations.1

A further presentation will focus on results from a Phase II study that investigates the potential of a future fixed-dose combination (FDC) of tiotropium and Boehringer Ingelheimas once-daily LABA olodaterol in patients with COPD. This Phase II trial was looking at the impact of different doses of tiotropium and olodaterol as a free combination on lung function, both administered individually by the Respimat SMI. Boehringer Ingelheim has already started to evaluate the tiotropium and olodaterol FDC in the TOviTOTM Phase III clinical trial programme.

In addition, a new analysis of the four year UPLIFTTM data will be presented. This study evaluated the effect of tiotropium (18 g via HandiHaler) in low risk patients based on the newly defined patient groups in the updated report of the Global Initiative for Chronic Obstructive Lung Disease (GOLD). It will further add to the wealth of data for tiotropium in COPD, which has now been investigated in 175 clinical trials in COPD.

The ERS congress is the largest respiratory meeting in the World, with attendance from more than 100 countries.2 All tiotropium abstracts can be accessed through the ERS website, [ http://www.erscongress2012.org/ ].

Asthma

Topic Lead Author Presentation details

Exacerbation data from two
Phase III studies evaluating
efficacy of once-daily
tiotropium in severe
asthma patients
symptomatic despite
ICS/LABA therapy

HAM Kerstjens Poster discussion

Monday 3rd September

08.30-10.30

Lung function data from
two Phase III studies
evaluating efficacy of once-
daily tiotropium in severe
asthma patients
symptomatic despite
ICS/LABA therapy

HAM Kerstjens Poster session

Monday 3rd September

12.50-14.40

COPD

Topic Lead Author Presentation details

Dose-finding study for
tiotropium and olodaterol
when administered in
combination via the
Respimat inhaler in
patients with COPD

R Aalbers Poster discussion

Monday 3rd September

14.45-16.45

Effectiveness of tiotropium
in low-risk patients
according to new GOLD
severity grading

D Halpin Poster session

Monday 3rd September

12.50-14.40

a" Ends a"

Please click on the link below for aNotes to Editorsa:

[ www.boehringer-ingelheim.com/news/news_releases/press_releases/2012/27_august_2012_tiotropium.html ]

References

1. Rabe, KF, Vermeire, PA, Soriano, JB, et al Clinical management of asthma in 1999: the Asthma Insights in Europe (AIRE) study.Eur Respir J 2000; 16, 802-807

2. [ http://www.erscongress2012.org/ ] (accessed 07/06/2012)


A Tiotropium is not licensed for the treatment of asthma

B The combination of tiotropium and olodaterol is not licensed for the treatment of COPD

C Inhaled corticosteroids

D Long-acting beta2-agonists


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