Condition: Cystic Fibrosis · Sponsor: Vertex Pharmaceuticals Incorporated
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of single dose of VX-581 and multiple ascending doses of VX-581 alone and in combination with tezacaftor (TEZ)/deutivacaftor (D-IVA) or D-IVA for up to ten days.
This description comes directly from the study's public registry record.
Medical Information · 617-341-6777 · medicalinfo@vrtx.com
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| Altasciences - Kansas City | Overland Park, Kansas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07283770