Archive for the 'Cystic Fibrosis' Category


ARIKACE™ Demonstrates Sustained Benefit In Multiple Studies And Over Multiple Cycles Of Treatment Of Pseudomonas Lung Infections

Transave, Inc., reported positive clinical trial results on its lead investigational drug, ARIKACE™ (liposomal amikacin for inhalation), an antibiotic that is entering Phase III development for the treatment of chronic lung infections...
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10/22/2010 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

Data To Be Presented At ERS Conference Highlights Potential For Denufosol To Benefit Cystic Fibrosis Patients On Minimal Pharmacotherapy

Inspire Pharmaceuticals, Inc. (NASDAQ: ISPH) announced today that data will be presented on denufosol tetrasodium, an investigational therapy for cystic fibrosis (CF), during oral and poster presentations at the European Respiratory Society (ERS) Annual Congress September 18 - 22, 2010 in Barcelona, Spain...
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09/21/2010 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

In Cystic Fibrosis Patients, Vitamin D May Treat And Prevent Allergic Reaction To Mold

Vitamin D may be an effective therapy to treat and even prevent allergy to a common mold that can cause severe complications for patients with cystic fibrosis and asthma, according to researchers from Children's Hospital of Pittsburgh of UPMC, the University of Pittsburgh School of Medicine and Louisiana State University School of Medicine. Results of the study, led by Jay Kolls, M.D., Ph.D...
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08/29/2010 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

ARIKACE™ Demonstrates Sustained Benefit In The Treatment Of Cystic Fibrosis Patients Who Have Pseudomonas Lung Infections

Transave, Inc., reported interim results from a multi-cycle Phase II open label clinical trial in cystic fibrosis (CF) patients on its lead investigational drug, ARIKACE™ (liposomal amikacin for inhalation)...
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06/19/2010 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

MP-376 Safe And Effective For Treatment Of P. Aeruginosa In CF Patients

New possible treatment to treat P. aeruginosa in cystic fibrosis (CF) patients appears to be promising, according to research to be presented at the ATS 2010 International Conference in New Orleans. Approximately 80 percent of CF patients develop chronic P. aeruginosa lung infection, and antibiotic resistance is an increasing problem...
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05/17/2010 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

Pigs Provide Clues On Cystic Fibrosis Lung Disease

Aided by a new experimental model, scientists are a step closer to understanding how cystic fibrosis (CF) causes lung disease in people with the condition. The findings, published online April 28 in the journal Science Translational Medicine, could help improve treatments for lung disease, which causes most of the deaths and disability among people with CF...
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04/29/2010 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

$1.4 Million Grant Received By Boston University School Of Medicine

Boston University School of Medicine's (BUSM) Pulmonary Center has received a two-year $1.4 million grant from the National Heart, Lung, and Blood Institute to derive stem cells and lung progenitors from patients with lung disease...
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12/25/2009 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

$1.4 Million Grant Received By Boston University School Of Medicine

Boston University School of Medicine's (BUSM) Pulmonary Center has received a two-year $1.4 million grant from the National Heart, Lung, and Blood Institute to derive stem cells and lung progenitors from patients with lung disease...
(more...)


12/25/2009 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

Cystic Fibrosis Protein’s Secret Life Revealed, US Study

Researchers have made an important discovery about the secret life of the defective protein that causes cystic fibrosis: while scientists already knew that CFTR protein regulates the acid-alkali balance in cells, what they didn't know, until this study revealed it, was what turns that ability on and off...
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12/22/2009 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

Cystic Fibrosis Protein’s Secret Life Revealed, US Study

Researchers have made an important discovery about the secret life of the defective protein that causes cystic fibrosis: while scientists already knew that CFTR protein regulates the acid-alkali balance in cells, what they didn't know, until this study revealed it, was what turns that ability on and off...
(more...)


12/22/2009 | Respiratory & Asthma - Cystic Fibrosis | Trackback | Comments Off

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