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June 16, 2014 News by Patrícia Silva, PhD

Annual European Cystic Fibrosis Conference Gathers International Research Community

Last Wednesday, the 37th European Cystic Fibrosis Conference gathered leading CF caregivers and researchers in Gothenburg, Sweden. The four-day program included seminars, round table talks, Meet the Expert sessions, and a physiotherapy short course, in order to facilitate acquisition and distribution of new knowledge and research in…

June 16, 2014 News by Charles Moore

Study Finds Probiotic Supplementation For CF Patients Can Help Improve Quality Of Life

A recent study published in the Iranian Journal of Pediatrics suggests that taking probiotics supplements can help improve quality of life for patients with cystic fibrosis (CF). Persons with CF (and many other disease conditions) frequently suffer from imbalanced intestinal microbiota ecosystems and suffer consequent dysregulated immune functionalities exacerbated…

June 16, 2014 News by Maureen Newman

Four Studies of Vertex’s Kalydeco Presented at European Cystic Fibrosis Society Conference

At the 37th European Cystic Fibrosis Society Conference, held June 11-14 in Sweden, representatives from Vertex Pharmaceuticals Inc. presented data from multiple clinical trials evaluating Kalydeco (ivacaftor) in patients with cystic fibrosis due to various mutations. “Not only does KALYDECO lead to significant initial improvements,…

June 13, 2014 News by Patrícia Silva, PhD

Transition to Adulthood Can Lead To Lapses In Care For Young CF Patients

Young people who suffer from physical disabilities or illnesses, such as cystic fibrosis, don’t always receive all of the necessary care and support they need to make a transition to care services. These are the conclusions of a study from the English Care and Quality Commission that reviewed…

June 12, 2014 News by Patrícia Silva, PhD

CFRI’s 27th National Cystic Fibrosis Conference Gathers Patients, Families and Researchers

For the 27th year, Cystic Fibrosis Research Inc. will hold a national conference to raise awareness of the disease and advocate for continued research and drug development. “Changing the Faces of Cystic Fibrosis: Inspiring Hope” will take place in San Francisco from August 1st through the 3rd, with several presentations designed…

June 12, 2014 News by Maureen Newman

Aptalis Pharma Studies Panzytrat in Cystic Fibrosis Patients in Phase 4 Trial

Aptalis Pharma continued to evaluate its pancreatic enzyme products (PEPs) in patients with cystic fibrosis and exocrine pancreatic insufficiency in its Phase 4 clinical trial of Panzytrat® 25,000. Results show that patients taking Panzytrat had better control over their steatorrhea, or fecal fat content. The study was designed to…

June 11, 2014 News by Maureen Newman

Pancreatic Enzyme Products May Benefit Cystic Fibrosis Patients with Malabsorption

After the Food and Drug Administration (FDA) issued rules requiring approval of pancreatic enzyme products (PEPs) in 2004, the cost and availability of the products added another hardship to the lives…

June 10, 2014 News by Maureen Newman

Health-Related Quality of Life is Affected in Adolescents With Cystic Fibrosis

A number of factors influence the health-related quality of life of patients with cystic fibrosis. A new study in the Italian Journal of Pediatrics written by a collaboration of researchers…

June 9, 2014 News by admin

Gilead’s AZLI Therapy For Treatment Of PALS In Cystic Fibrosis Deemed Safe, Effective In Recent Study

Following the recent success of a phase 3b clinical trial for Aztreonam in cystic fibrosis (CF) patients with Burkholderia infections, Gilead Sciences, Inc., a research-based biopharmaceutical company engaged in CF drug discovery and development, completed another phase 3 clinical trial to evaluate the safety of inhalable Aztreonam (AZLI)…

June 5, 2014 News by Maureen Newman

Vertex’s Ivacaftor Benefits Residual Function Mutation Cystic Fibrosis Patients in First-of-Kind Study

Vertex Pharmaceuticals‘ two-part proof-of-concept study evaluating ivacaftor (under the name KALYDECO) in 24 cystic fibrosis patients shows data consistent with previous preclinical observations. An eight-week open-label period resulted in improved lung function in patients, initiating plans for a future Phase 3 trial. Each of the 24…

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