There may be hope for those with cystic fibrosis, as researchers have discovered a drug that targets the cause of the lung disease, reports HealthDay.
The condition, which affects the exocrine glands and causes mucosal buildup within the lungs and other organs, is caused by a “faulty protein.” Ivacaftor is the new medication that reportedly improves cystic fibrosis and reduce its symptoms.
“It has a huge significance for the whole cystic fibrosis community,” Bonnie Ramsey, a professor and doctor in Seattle who authored the study, told the source. “It’s the first time we have developed a therapy directed at the abnormal proteins and showing that it can be corrected.
This research is good news for the 5 percent of cystic fibrosis patients who were born with a specific protein that leads to the disease, as approval by the Food and Drug Administration could lead to improved health and a longer life expectancy.
The study published in this week’s New England Journal of Medicine showed improvements in participants health in just two weeks, with some patients experiencing better lung function and hydration. Increased hydration helps clear the mucus out of one’s airways.
Ivacaftor is currently pending approval by the FDA and will be manufactured under the brand name Kalydeco by Vertex Pharmaceuticals. The drugmaker has applied for expedited approval and is expecting a decision to be made by April.
Further testing of Ivacaftor is currently underway to study its effects in conjunction with other medications, reports the news provider.

