Can a sugar mimic fix cystic fibrosis?
NCT ID NCT02325362
First seen Nov 20, 2025 · Last updated Apr 28, 2026 · Updated 17 times
Summary
This study tested a drug called miglustat in 16 adults with cystic fibrosis who have a specific genetic mutation (F508del). The goal was to see if miglustat could help restore the function of a faulty protein that controls salt and water movement in the lungs. Researchers measured changes in nasal electrical activity as a sign of improvement. The study was small and early-stage, so more research is needed to know if it truly helps patients.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Assistance publique-Hôpitaux de Paris, Hôpital Cochin
Paris, 75014, France
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