Cystic fibrosis, a common lethal genetic disorder, is characterized by a neutrophilic inflammatory exudate in the airways which causes bronchiectasis and eventual respiratory failure. Neutrophil elastase is believed to mediate many of the pathologic processes such as destruction of airway supporting tissue, mucus hypersecretion, opsonic deficiency, and cytokine secretion. DMP777 is a synthetic monobactam that penetrates the neutrophil to inhibit both intra- and extracellular elastase in a selective and essentially irreversible fashion. This study is a dose-escalating protocol to examine safety, pharmacokinetics, and pharmacodynamics of DMP777 in patients with CF by direct measurement of drug levels and elastase inhibition in bronchoalvolar fluids.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000070-37S2
Application #
6264332
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
37
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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