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Clinical Trial Finder
Blaze a trail to better treatments and a cure for cystic fibrosis.
As a clinical trial volunteer, you are paving the way for new treatments. Search or filter for trials that may be right for you, or learn more about what it means to be a trailblazer.
Showing 1-6 of 199 studies
As a clinical trial volunteer, you are paving the way for new treatments. Search for trials that may be right for you using the filter on the left, or learn more about what it means to be a trailblazer.
Showing 1-6 of 199 studies
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Restore CFTR FunctionEnrolling
Phase 3 study of long-term ivacaftor in babies who have a CFTR gating mutation , protocol number Vertex VX-770-126This open-label study is taking place at multiple care centers across the U.S. It will look at the safety and effectiveness of long-term ivacaftor in babies who have a CFTR gating mutation.
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Age:
Less than 25 Months
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Mutation(s):
One Copy F508del or No Copies F508del
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FEV1% Predicted:
No FEV1 Limit
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Number of Visits:
18
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Length of Participation:
128 weeks
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Anti-InflammatoryEnrolling
Study of INS1007/brensocatib tablets in adults with CF , protocol number Insmed INS1007-211This study will look at the safety, tolerability, and how the body processes INS1007/brensocatib tablets, a drug intended to reduce inflammation.
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Age:
18 Years and Older
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Mutation(s):
No Mutation Requirement
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FEV1% Predicted:
40 to 90%
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Number of Visits:
8
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Length of Participation:
56 days
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Anti-InfectiveEnrolling
Study to evaluate nebulized BX004-A in adults with cystic fibrosis and chronic Pseudomonas aeruginosa (BiomX Phase 1b/2a) , protocol number BiomX BMX-04-001 Part 1This study is testing the safety and tolerability of nebulized BX004-A, a bacteriophage drug intended to treat infections in the lung. Bacteriophages are specialized viruses that kill very specific bacterial strains. Multiple doses of the drug will be tested in adults with cystic fibrosis and chronic Pseudomonas aeruginosa (PsA) to find the best dose.
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Age:
18 Years and Older
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Mutation(s):
No Mutation Requirement
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FEV1% Predicted:
40% or greater
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Number of Visits:
7
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Length of Participation:
189 days
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Nutritional-GIEnrolling
Study to evaluate Creon in adults with cystic fibrosis or chronic pancreatitis , protocol number AbbVie M21-432This study will look at the symptoms of exocrine pancreatic insufficiency (EPI) in adults with cystic fibrosis or chronic pancreatitis treated with Creon with an alternate source of active drug. Creon is a drug approved to treat EPI.
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Age:
18 Years and Older
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Mutation(s):
No Mutation Requirement
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FEV1% Predicted:
No FEV1 Limit
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Number of Visits:
3
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Length of Participation:
142 days
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ObservationalEnrolling
PREDICT: NTM observational study , protocol number NTM-OB-17 (PREDICT)This study is taking place at multiple care centers across the U.S. It will evaluate the current standard of diagnosing nontuberculous mycobacteria (NTM) in people with CF.
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Age:
6 Years and Older
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Mutation(s):
No Mutation Requirement
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FEV1% Predicted:
No FEV1 Limit
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Number of Visits:
20
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Length of Participation:
5 years
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OtherEnrolling
Study of SPI-1005 in people with CF ages 18 and older , protocol number Sound Pharma SPI-3005-501.2This study will test the safety and tolerability of SPI-1005, a drug intended to prevent and treat hearing loss caused by aminoglycosides.
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Age:
18 Years and Older
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Mutation(s):
No Mutation Requirement
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FEV1% Predicted:
40% or greater
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Number of Visits:
6
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Length of Participation:
49 days
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Showing 1-6 of 199 studies
Studies in this tool are multi-center studies facilitated by the Cystic Fibrosis Therapeutics Development Network. For a complete list of cystic fibrosis related studies, visit www.clinicaltrials.gov.
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