Spirovant Sciences, a gene therapy company developing treatments and cures for genetic lung diseases including cystic fibrosis, today announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug and Rare Pediatric Disease Designations to its lead product candidate, SPIRO-2101, for the treatment of cystic fibrosis. SPIRO-2101, an inhaled […]
Tag: CYSTIC FIBROSIS
International Study Suggests People With CF Have Lower COVID-19 Incidence
The Cystic Fibrosis Foundation announced data from a collaborative, international effort to understand the impact of COVID-19 on people with cystic fibrosis, a genetic disease that impacts the lungs and other organs. The manuscript, published in the Journal of Cystic Fibrosis, reports on 40 people with CF across eight countries […]
Electromed Launches SmartVest Connect Mobile Application
Electromed, Inc. has announced the launch of its SmartVest Connect® App for iOS and Android, a personalized high-frequency chest wall oscillation (HFCWO) therapy management portal for patients with compromised pulmonary function. The SmartVest Connect app securely connects to the SmartVest® SQL® through Bluetooth™ technology. This interface allows patients and healthcare teams to […]
CF Foundation Support Development of Malabsorption Syndrome Therapy
Synspira Therapeutics Inc. has signed an agreement with the Cystic Fibrosis Foundation to support the development of SNSP003, Synspira’s orally delivered non-porcine enzyme replacement therapy (ERT) designed to treat Malabsorption Syndromes. Malabsorption Syndromes are a group of life-threatening disorders that result from defects in the digestion and absorption of macronutrients […]
CF Patients Experience Improved Lung Health with Lumacaftor-Ivacaftor But with Caveats
In adolescent and adult patients with cystic fibrosis taking lumacaftor-ivacaftor (ORKAMBI®), the combination drug appears to improve lung function and body weight and reduce the need for intravenous antibiotic treatment, according to a French study published online in the American Thoracic Society’s American Journal of Respiratory and Critical Care Medicine. However, […]
Ivacaftor May Reduce Common Infections in Patients with CF
Patients with cystic fibrosis who take ivacaftor appear to have fewer respiratory infections over time than those not taking the drug, according to new research published online in the Annals of the American Thoracic Society. Cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Ivacaftor […]
International Biophysics Renews Commitment to Growing CF and Mobile HFCWO Awareness
International Biophysics Corporation, manufacturer of the AffloVest is committed to raising awareness of Cystic Fibrosis and the importance of airway clearance therapy in the management of the disease. Over 30,000 people in the U.S. and 70,000 worldwide struggle with the effects of cystic fibrosis every day. There is no cure […]
May is National CF Awareness Month: Transplant Helps Georgia Woman Win Her Battle
May is National Cystic Fibrosis (CF) Awareness Month. More than 30,000 adults and kids in the United States have CF. In Georgia, a CF survivor is currently winning her 35-year battle with the disease — thanks to her life-saving double lung transplant. Today, on May Day, she and her husband […]
Hospital Transforming Cystic Fibrosis Remote Care
A pioneering approach to cystic fibrosis (CF) care saves on the cost and inconvenience of frequent hospital visits and could help detect changes in lung function sooner. These results come from a pilot study involving people with CF who are being treated at London’s Royal Brompton Hospital. The results come […]
FDA Approves ORKAMBI®, First Medicine to Treat the Underlying Cause of CF for Children Ages 2-5 Years with Most Common Form of the Disease
Vertex Pharmaceuticals Incorporated announced the U.S. Food and Drug Administration (FDA) has approved ORKAMBI® (lumacaftor/ivacaftor) to include use in children ages 2 through 5 years with cystic fibrosis (CF) who have two copies of the F508del-CFTR mutation, making it the first medicine approved to treat the underlying cause of CF […]












