A Phase 1, First-in-human Study of VX-668
NCT05727800 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 114
Last updated 2024-03-15
Summary
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of VX-668 at various doses.
Conditions
- Alpha-1 Antitrypsin Deficiency
Interventions
- DRUG
-
VX-668
Suspension for oral administration.
- DRUG
-
Suspension for oral administration.
Sponsors & Collaborators
-
Vertex Pharmaceuticals Incorporated
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-02-08
- Primary Completion
- 2023-09-12
- Completion
- 2024-02-13
- FDA Drug
- Yes
Countries
- United States
Study Locations
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