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Restore CFTR ProteinClosed to Enrollment
Study of galicaftor/navocaftor/ABBV-576 combination therapy in adults with cystic fibrosis who have at least one F508del mutation and are on stable elexacaftor/tezacaftor/ivacaftor (Trikafta) treatment., protocol number Abbvie M19-771The following information will be used to determine eligibility for this study. Fill out the form and click “Preview Message.” This will draft an email you can send directly to the Research Coordinator. Please note, this does not guarantee entry into this particular study.
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Restore CFTR ProteinClosed to Enrollment
Study of galicaftor/navocaftor/ABBV-576 combination therapy in adults with cystic fibrosis who have at least one F508del mutation and are on stable elexacaftor/tezacaftor/ivacaftor (Trikafta) treatment., protocol number Abbvie M19-771
This study will look at the safety and effectiveness of galicaftor/navocaftor/ABBV-576 combination therapy, a combination of CFTR modulators intended to help CFTR protein function closer to normal. This study is for adults with cystic fibrosis who have at least one F508del mutation.
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Age:
18 Years and Older
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Mutation(s):
Two Copies F508del or One Copy F508del
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FEV1% Predicted:
40 to 90%
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Number of Visits:
6
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Length of Participation:
3 months
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