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RECRUITING
NCT07437105
PHASE1
Dose Escalation Study Evaluating the Safety and Pharmacokinetics of VX-272 in Healthy Participants
Sponsor: Vertex Pharmaceuticals Incorporated
View on ClinicalTrials.gov
Summary
The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics of single and multiple ascending doses of VX-272.
Official title: A Phase 1, Randomized, Double-blind, Placebo-controlled, Dose Escalation Study Evaluating Safety and Pharmacokinetics of VX-272 in Healthy Subjects
Key Details
Gender
All
Age Range
18 Years - 55 Years
Study Type
INTERVENTIONAL
Enrollment
128
Start Date
2026-02-25
Completion Date
2027-03-23
Last Updated
2026-03-31
Healthy Volunteers
Yes
Conditions
Interventions
DRUG
VX-272
Suspension for Oral Administration.
DRUG
Placebo
Suspension for Oral Administration.
Locations (1)
Celerion - Tempe
Tempe, Arizona, United States