Drug Development Pipeline
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Restore CFTR Function
This program is developing potential CFTR modulators, a type of drug designed to fix the defective CFTR protein. These new modulators could benefit people with the most common CF-causing mutation, F508del, and may eventually offer an alternative to currently approved modulators.
Laboratory studies to develop and test these compounds are underway.
This program is sponsored by Sionna Therapeutics and partially funded by the Cystic Fibrosis Foundation.
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