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Chronic Lung Disease - Axentis Pharma Attracts Investment Interest
Date:2/2/2009

ell is triggered when the liposomes attach to the outer cell membrane. Tobramycin then penetrates into the inner cell compartment of the microbial cell, which leads to rapid cell death.

About cystic fibrosis

Cystic fibrosis is the most common life-threatening hereditary disease amongst Caucasian populations. The disease is caused by a mutation in the CFTR (cystic fibrosis transmembrane conductance regulator) gene found on chromosome 7. This mutation causes increased secretion deposits on mucous membranes. Lung complications represent the most serious manifestation of the disease - and the reason for the high mortality rate amongst patients. Such complications often involve infection of the bronchi by the bacteria Pseudomonas aeruginosa. Chronic inflammations then cause lung functions to become blocked. In addition to the breakdown of lung tissue, this also leads to bronchiectasis and lung failure.

    For further information, please contact:

    Axentis Pharma AG
    Limmatquai 138
    8001 Zurich
    Switzerland
    T: +41-79-525-6668
    E board@axentispharma.com

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    PR&D - Public Relations for Research & Education
    Campus Vienna Biocenter 2
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