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Cystic Fibrosis Foundation Launches Ambitious Effort To Increase Participation In Clinical Trials

Cystic Fibrosis Foundation recently announced an important initiative to double the number of people with cystic fibrosis who participate in clinical trials over the next two years.”To help potential new drugs for CF move swiftly from the research stage into the hands of patients who need them, we need more people with cystic fibrosis to take part in clinical trials,” said Robert J. Beall, Ph.D, president and CEO of the CF Foundation.

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Posted in Cystic Fibrosis on Jul 13th, 2007, 3:00 am     

Genaera Discontinues LOMUCIN(TM) In Cystic Fibrosis And Squalamine In Prostate Cancer Studies

Genaera Corporation (Nasdaq: GENR) today announced that, in conjunction with Cystic Fibrosis Foundation Therapeutics, Inc. (CFFT), both parties have agreed for reasons of futility to discontinue the Phase 2 study of LOMUCIN(TM) for the treatment of cystic fibrosis (CF). Genaera also announced that the Phase 2 study of squalamine in prostate cancer, which is an investigator-initiated study funded by the Department of Defense, will also be discontinued.

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Posted in Cystic Fibrosis on Jul 6th, 2007, 2:00 am     

Florida To Begin Newborn Screening For Cystic Fibrosis

The state of Florida will begin screening all newborns for cystic fibrosis (CF) starting July 1. Florida joins 36 other states in the country, plus the District of Columbia, to routinely screen for CF at birth. “This is the right thing to do,” said Peter Hodge, a Boca Raton, Fla. father of two daughters with CF. Hodge’s 14-year-old daughter, Olivia, wasn’t diagnosed with the disease until she was a teenager. “We wish our daughter had been diagnosed at birth.

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Posted in Cystic Fibrosis on Jun 29th, 2007, 2:00 am     

Eurand’s Zentase(TM) Effective In Treating Exocrine Pancreatic Insufficiency, Studies Show

Eurand N.V. (Nasdaq: EURX) today announced results that were presented at the recent European Cystic Fibrosis Society meeting in Antalya, Turkey, held June 13-16. Results from two phase III studies of Zentase(TM) (EUR-1008) showing a statistically and clinically significant improvement in the absorption of fat, protein and nutrients in patients suffering from Exocrine Pancreatic Insufficiency (EPI).

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Posted in Cystic Fibrosis on Jun 20th, 2007, 2:00 am     

PARI Pharma Presents Study Results Of Sinus Delivery And Inhaled Liposomal Ciclosporin A At European Cystic Fibrosis Conference

PARI Pharma will present in-vivo study results for their PARI SINUS pulsating drug delivery system as well as lung deposition and pharmacokinetic data of their proprietary inhaled liposomal Ciclosporin A formulation in lung transplant patients at the European Cystic Fibrosis Conference (ECFC) in Belek, Turkey this week.

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Posted in Cystic Fibrosis on Jun 15th, 2007, 2:00 am     

Evidence Of Early Onset Of Poor Bone Mineralization Revealed In Children With Cystic Fibrosis

In a study of children with cystic fibrosis, French researchers found evidence of very early onset defective bone mineralization in the lumbar spine that was not caused by either nutritional status or lung disease. The lumbar spine is that part of the back between the ribs and the pelvis.

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Posted in Cystic Fibrosis on May 5th, 2007, 10:00 pm     

Key Found To Kill Cystic Fibrosis Superbug

Researchers from the Schulich School of Medicine & Dentistry at The University of Western Ontario , working with a group from Edinburgh, have discovered a way to kill the cystic fibrosis superbug, Burkholderia cenocepacia. These investigators, under the leadership of Dr. Miguel Valvano, Department of Microbiology and Immunology, have had their research published in the May issue of the Journal of Bacteriology, and highlighted in Nature Reviews/Microbiology. B.

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Posted in Cystic Fibrosis on Apr 26th, 2007, 2:00 am     

Study On Lung-Infecting Bacterial Enzyme Suggests New Approach To Cystic Fibrosis Treatment

Researchers at the University of Pennsylvania School of Medicine have discovered that an enzyme produced by lung-infecting bacteria further shuts down a protein that is defective in cystic fibrosis patients. The disruption to this protein that conveys ions from lung cells to airways causes thick mucus to buildup inside the lung. The finding suggests a new therapeutic target for treating lung infections in some cystic fibrosis (CF) patients.

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Posted in Cystic Fibrosis on Apr 25th, 2007, 3:00 am     

Penn Study On Lung-Infecting Bacterial Enzyme Suggests New Approach To Cystic Fibrosis Treatment

Researchers at the University of Pennsylvania School of Medicine have discovered that an enzyme produced by lung-infecting bacteria further shuts down a protein that is defective in cystic fibrosis patients. The disruption to this protein that conveys ions from lung cells to airways causes thick mucus to buildup inside the lung. The finding suggests a new therapeutic target for treating lung infections in some cystic fibrosis (CF) patients.

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Posted in Cystic Fibrosis on Apr 20th, 2007, 2:00 pm     

Cystic Fibrosis Foundation Launches GREAT STRIDES Walks In 550 Locations Nationwide, USA

The Cystic Fibrosis Foundation announced today the kick-off of GREAT STRIDES, a national walk benefiting critical cystic fibrosis research, education and care programs. GREAT STRIDES, now in its 19th year, is the largest CF fund-raiser and seeks to raise $36 million nationwide in 2007. Tens of thousands of walkers are expected to turn out at 550 walk sites nationwide from March to June. Some walks will coincide with National Cystic Fibrosis Awareness Month in May.

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Posted in Cystic Fibrosis on Apr 20th, 2007, 12:00 pm     

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