Clinical Trial

Dose Escalation Study Evaluating the Safety and Pharmacokinetics of VX-272 in Healthy Participants

Recruiting Phase 1
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Summary
The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics of single and multiple ascending doses of VX-272.
Protocol Amendment History 1 change
critical Recruitment opened 2026-04-01
Trial Details
NCT Number NCT07437105
Lead Sponsor Vertex Pharmaceuticals Incorporated
Conditions Cystic Fibrosis
Enrollment 128 participants
Start Date 2026-02-25
Primary Completion 2027-03-23 (estimated)
Study Completion 2027-03-23 (estimated)
Updated on ClinicalTrials.gov 2026-03-31