WATCH: New Developments in Drugs to Restore Airway Surface Liquid, March 2016

Dr. John P. Clancy shares new developments in drugs that restore airway surface liquid in the lungs of people with cystic fibrosis, making it easier to clear mucus.

| 1 min read
Christina-Roman
Christina Roman
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Welcome to the third installment in our video series highlighting the ways that Cystic Fibrosis Foundation Therapeutics (CFFT) and industry are tackling cystic fibrosis from every angle. This week's topic explores new approaches to restoring airway surface liquid that are in CFFT's drug development pipeline.

Watch the video below to hear Dr. John P. Clancy describe how the airway surfaces in the lungs of people with CF become dehydrated and why it is important to restore liquid to those surfaces. Dr. Clancy describes two new research approaches being tested in clinical trials that may help correct this problem.

If you haven't already, check out the previous posts on restoring CFTR function and reducing inflammation. And stay tuned for more videos about ongoing research.

To learn more about drugs that are in development, visit our drug development pipeline. Or if you would like to search for a clinical trial, visit the Clinical Trial Finder.

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Topics
Research | Drug Pipeline | Clinical Trials | Our Research Approach
Christina-Roman

As community engagement manager for the Cystic Fibrosis Foundation, Christina works to help embed the voice of the community into the work of the Foundation. Before joining the community partnerships team Christina worked on the clinical trials team for 3 years and at Colorado Children's Hospital for 2 years supporting the CF team. She holds a master's degree in public health from the University of Colorado. Originally from Estes Park, Colo., Christina now lives in Washington, D.C., with her husband.

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This site contains general information about cystic fibrosis, as well as personal insight from the CF community. Opinions and experiences shared by members of our community, including but not limited to people with CF and their families, belong solely to the blog post author and do not represent those of the Cystic Fibrosis Foundation, unless explicitly stated. In addition, the site is not intended as a substitute for treatment advice from a medical professional. Consult your doctor before making any changes to your treatment.