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Mpex Candidate, MP-376, Granted U.S. Orphan Drug Status For The Treatment Of Cystic Fibrosis
Mpex Pharmaceuticals, Inc.  
announced that the U.S. Food and Drug Administration's (FDA) Office of 
Orphan Products Development has granted Mpex orphan drug designation for  
levofloxacin solution for inhalation for the treatment of pulmonary 
infections due to Pseudomonas aeruginosa and other bacteria in patients 
with cystic fibrosis. Levofloxacin is the active pharmaceutical ingredient 
in MP-376, the company's proprietary levofloxacin solution for inhalation.
 
    
Patients with cystic fibrosis (CF) suffer from chronic infections of 
the lower respiratory tract that can be caused by one or multiple bacteria,  
including Pseudomonas aeruginosa. Chronic pulmonary infections are 
difficult to eradicate and are implicated as the major cause of 
deterioration of pulmonary function and associated morbidity and mortality 
in CF patients. Chronic infection is associated with pulmonary 
exacerbations due to bacterial overgrowth, and a decrease in lung function 
over time from inflammation triggered by bacteria and their toxins.
 
    
"Obtaining orphan drug designation for MP-376 in cystic fibrosis is an 
important milestone for the program," stated Daniel Burgess, President and  
Chief Executive Officer of Mpex Pharmaceuticals, Inc. "This helps reinforce 
our belief that MP-376 has the potential to provide a valuable new 
treatment option in the management of cystic fibrosis. We look forward to 
working with CF patients, treatment providers and the FDA to rapidly 
advance this product candidate through to commercialization."
 
    
Orphan status is granted by the FDA to promote the development of  
products that demonstrate promise for the treatment of rare diseases 
affecting fewer than 200,000 Americans annually. Orphan drug designation 
will entitle Mpex to a seven-year period of exclusive marketing rights for 
MP-376 for the orphan indication following the date of the drug's marketing 
approval by the FDA. Orphan status also enables Mpex to apply for research 
funding, tax credits for certain research expenses, and a waiver from FDA 
user fees.
 
    
About MP-376
    
MP-376 is a proprietary formulation of levofloxacin that has been 
designed by Mpex scientists to enable aerosol administration. Levofloxacin  
is a powerful antibiotic that has been widely used in a variety of 
indications for over a decade and has established safety and efficacy when 
administered orally or intravenously against many bacterial pathogens 
including Pseudomonas aeruginosa. Administration of MP-376 with a high 
efficiency nebulizer to the lungs allows for the delivery of high 
concentrations of active drug directly to the site of infection, while 
minimizing systemic exposure. Mpex believes this approach has the potential 
to improve bacterial killing and reduce resistance development versus 
traditional oral or IV routes of administration.
  
    
Mpex recently completed a multi-center, 14-day placebo controlled 
clinical trial with MP-376 in 40 CF patients. Based on these results and 
consultations with the FDA and the Therapeutics Development Network (TDN) 
of the Cystic Fibrosis Foundation, the company expects to initiate a Phase 
2b clinical trial in approximately 140 CF patients in the second quarter of 
2008. Several dosing regimens of MP-376 will be compared, including once 
daily administration schedules. Results from this trial, if successful, are 
expected to enable the company to select dosing regimens for the pivotal 
Phase 3 clinical program in this indication.
 
    
About Mpex Pharmaceuticals
    
Mpex Pharmaceuticals is a clinical stage biopharmaceutical company 
whose mission is to develop important new therapies to combat the growing  
issue of antibiotic resistance. The company's internal development pipeline 
focuses on combining proprietary formulations, PK/PD strategies and novel 
potentiating agents with proven antibiotics to overcome or directly inhibit 
the molecular mechanisms in bacteria responsible for antibiotic resistance. 
Mpex's lead product candidate, MP-376, is being developed clinically for 
the aerosol treatment of chronic respiratory tract infections such as those 
found in cystic fibrosis patients. The company has also built a discovery 
and development platform and intellectual property estate around inhibitors 
of bacterial multi-drug resistant (MDR) efflux pumps (EPIs). Bacterial 
efflux of antibiotics is a leading source of multi-drug resistance, 
particularly in gram-negative organisms. Mpex compounds have been shown 
preclinically to overcome efflux-based resistance to multiple classes of 
antibiotics in both in vitro and in vivo studies.
  
Mpex Pharmaceuticals, Inc.
http://www.mpexpharma.com
		
Mpex candidate, MP-376, SUA a acordat statutul de orfan de droguri, pentru tratamentul de fibroza chistica - Mpex Candidate, MP-376, Granted U.S. Orphan Drug Status For The Treatment Of Cystic Fibrosis - articole medicale engleza - startsanatate