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Annual Report 2005 - Boehringer Ingelheim

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IMP scientists are at the forefront of discovery<br />

defining fundamental processes of cell division<br />

and differentiation in healthy and diseased states.<br />

A collaboration started in 2001 between the IMP<br />

and the Institute of Molecular Biotechnology<br />

Austria (IMBA) added a new dimension to our<br />

academic network. Intensified interactions with<br />

IMBA began in <strong>2005</strong> in target identification<br />

using model organisms.<br />

The more than 3,000 scientists, technicians and<br />

support personnel we employ in preclinical R&D<br />

is complemented by about 2,100 clinical moni-<br />

tors, statisticians and data managers in clinical<br />

development and medical departments.<br />

Respiratory diseases<br />

Respiratory diseases have long been a major<br />

focus area for <strong>Boehringer</strong> <strong>Ingelheim</strong> and we<br />

dedicate ample resources for research in this field.<br />

Our main objective in pulmonary research is to<br />

provide still further improved treatment options<br />

for chronic obstructive pulmonary disease<br />

(COPD) and severe asthma. COPD is currently<br />

the fourth most common cause of death, yet up<br />

to three quarters of sufferers in Europe go<br />

undiagnosed. This suggests a major unmet need<br />

for treatment for this debilitating lung disease<br />

which often afflicts smokers. Our worldwide<br />

launch of tiotropium (spiriva®) provided a<br />

medication to improve COPD therapy, strength-<br />

ening our leading position in the bronchodilator<br />

field. This is being build up by developing<br />

bronchodilators with alternative mechanisms<br />

which additionally offer the opportunity<br />

for combination with our anticholinergic<br />

compounds.<br />

Extending our product portfolio to drugs that<br />

target treatment of the underlying inflammation<br />

and the tissue remodelling process are the 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. It is<br />

<strong>Boehringer</strong> <strong>Ingelheim</strong> A n n u A l R e p o R t 2 0 0 5<br />

only poorly controlled by current, widely-used<br />

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

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

mechanisms and immunological paradigms<br />

which would allow us to replace or reduce the<br />

doses of inhaled steroids by providing anti-<br />

inflammatory therapy better tolerated by patients.<br />

Another goal is to provide a new treatment for<br />

specific syndromes with high unmet medical<br />

need, such as severe, steroid-resistant asthma.<br />

virology<br />

Antiviral therapies for many serious, life-threat-<br />

ening chronic and acute viral diseases are lacking<br />

or are unsatisfactory. Our Laval centre focuses on<br />

the discovery and development of new antiviral<br />

therapeutics for the treatment of the human<br />

immunodeficiency virus type 1 (HIV-1) and the<br />

hepatitis C virus (HCV). These two devastating<br />

pathogens have each emerged epidemically in<br />

recent decades, afflicting millions globally.<br />

Our HCV research is directed toward identifying<br />

inhibitors targeting essential viral enzymes, such<br />

as the HCV serine protease and RNA polymerase.<br />

Such new mechanisms offer the potential for<br />

new therapies with improved safety and efficacy<br />

compared to current treatments of chronic<br />

hepatitis C. Our clinical studies with an HCV<br />

serine protease inhibitor provided the first proof<br />

of clinical concept for this class of antiviral agent<br />

and we continue to make efforts to exploit this<br />

antiviral target together with other novel<br />

approaches.<br />

Our R&D activities in HIV aim at developing new<br />

treatment options, especially for HIV patients<br />

who have failed prior therapy due to the develop-<br />

ment of drug resistance. Our research into the<br />

rapidly growing resistance problem has identified<br />

a promising new non-nucleoside reverse tran-<br />

scriptase inhibitor (NNRTI) as a follow-up to our<br />

existing HIV treatment viramune® (nevirapine).<br />

Development is proceeding on this compound<br />

which may become a treatment alternative for<br />

patients who have failed first line NNRTI therapy.

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