Custom drug testing offers hope for rare CF cases
NCT ID NCT04580368
Summary
This study aims to find effective treatments for people with rare cystic fibrosis gene mutations. Researchers will test existing CF drugs on patients' own nasal cells in the lab, then conduct personalized trials to see if those drugs help improve breathing. The goal is to match individual patients with treatments that work for their specific genetic makeup when standard approaches aren't available.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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CCHMC
RECRUITINGCincinnati, Ohio, 45203, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
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