New Ideas Energize Scientists at CF Research Conference

The Foundation hosted a small conference that brought together CF scientists, clinical researchers, and biotechnology and pharmaceutical industry representatives. Learn more and watch a short video of attendees sharing their thoughts about the progress we are making in CF research.

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Katherine Tuggle, Ph.D.
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Earlier this summer, the CF Foundation hosted a small research conference that brought together CF scientists, clinical researchers, and biotechnology and pharmaceutical industry representatives from around the world to discuss the latest advances and to outline the future direction of CF research. 

The meeting was centered around three main themes: 

  • Understanding how information from clinical trials of CFTR modulators -- drugs targeting the underlying cause of CF -- could help shape and direct basic laboratory research and lead to better design of CF clinical trials.
  • Exploring emerging technologies that could be applied to CF, including cutting-edge research on gene editing and gene delivery that offers the potential to correct the defective CF gene.
  • Identifying new research tools that will facilitate a better understanding of the disease process and accelerate development of new CF therapies. 

By the end, I felt renewed energy among the scientists as they exchanged ideas and discussed collaborations that will continue through the year. These individuals and their creative talents are critical to solving the complex puzzle of CF. It was particularly rewarding to see their eagerness and excitement to get back to their labs and start working on new ideas that emerged from the meeting.

This short video of conference attendees sharing their thoughts about the progress we are making in CF research captures the excitement of the conference and their commitment to continue working to find a cure.

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.

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Katherine has been involved with CF research since 2009 as both a graduate student and postdoctoral fellow at the University of Alabama at Birmingham. In 2014, she joined the Foundation to oversee its basic science research programs, including the 11 basic science research centers around the country. She is also involved in a number of Foundation initiatives focused on developing and validating model systems that may be used for personalized medicine. In her free time, Katherine enjoys traveling with her husband and spending time with her German shepherd.

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