27.10.2012 Views

Annual Report 2006 - Boehringer Ingelheim

Annual Report 2006 - Boehringer Ingelheim

Annual Report 2006 - Boehringer Ingelheim

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Our R & D for respiratory diseases<br />

Our worldwide launch of spiriva® (tiotropium)<br />

provided a medication to improve COPD therapy<br />

and strengthened our leading position in this field.<br />

We are striving for further innovations by devel-<br />

oping bronchodilators with alternative mecha-<br />

nisms. These new bronchodilators are being for-<br />

mulated in innovative inhalation devices.<br />

In addition, <strong>Boehringer</strong> <strong>Ingelheim</strong> in <strong>2006</strong> entered<br />

into a worldwide collaboration, development and<br />

licence agreement with the British company<br />

Vectura. The aim of the collaboration is to develop<br />

a multi-dose dry powder inhaler as a <strong>Boehringer</strong><br />

<strong>Ingelheim</strong> branded device, to deliver a range of<br />

proprietary <strong>Boehringer</strong> <strong>Ingelheim</strong> respiratory<br />

products, mainly for the treatment of COPD and<br />

asthma. We currently have numerous bronchodilator<br />

programmes in development, six of them<br />

in clinical studies.<br />

Extending our product portfolio to drugs that<br />

target treatment of the underlying inflammation<br />

and the tissue remodelling process are further key<br />

goals in our COPD research. Inflammation in<br />

COPD patients is provoked by an infiltration of<br />

the lungs by macrophages and neutrophils.<br />

This is only poorly controlled by current, widelyused<br />

anti-inflammatory drugs, such as corticosteroids.<br />

We are therefore working on alternative<br />

anti-inflammatory mechanisms, specifically targeting<br />

macrophage and neutrophil-driven inflammation.<br />

In addition, we aim at preventing or delaying tissue<br />

remodelling that is induced by chronic inflammation<br />

by targeting lung growth factors. Two<br />

first-in-class mechanisms targeting mucous<br />

hyperplasia and fibrosis are being tested clinically.<br />

Beyond COPD, such new mechanisms have a<br />

therapeutic potential in idiopathic pulmonary<br />

fibrosis (IPF), a life-threatening disease, and in<br />

<strong>Boehringer</strong> <strong>Ingelheim</strong> A n n u A l R e p o R t 2 0 0 6<br />

severe asthma, where mucous plugging is considered<br />

the main cause of death.<br />

Our research in asthma is aimed at new mechanisms<br />

and immunological paradigms that would<br />

allow us to replace or reduce the doses of inhaled<br />

steroids by providing anti-inflammatory therapy<br />

better tolerated by patients. Another goal is to<br />

provide a new treatment for specific syndromes<br />

with high, unmet medical need, such as severe,<br />

steroid-resistant asthma.<br />

Diseases of the<br />

central nervous system<br />

According to World Health Organization (WHO)<br />

predictions, diseases of the central nervous system<br />

will constitute an increasing medical need in this<br />

century, attributable to an exponential increase of<br />

these diseases in patients beyond 65 years of age,<br />

combined with an aging population. To date,<br />

available therapeutic treatments are still unsatisfactory<br />

for the majority of CNS diseases.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!