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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