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NCT06394167 · ClinicalTrials.gov registry record · Phase 1
A Phase 1 Dose Escalation Study of Intravenous VX-993 in Healthy Adults
A Phase 1 study, sponsored by Vertex Pharmaceuticals Incorporated.
- Completed
- Registry status
- Phase 1
- Development phase
- 88
- Enrollment target
NCT06394167 is a Phase 1 study that has completed, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 88 participants.
The verdict
NCT06394167, a Phase 1 study, has completed, sponsored by Vertex Pharmaceuticals Incorporated.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 88 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of intravenously administered VX-993 at different doses in healthy participants.
Interventions
- DRUG Placebo
- DRUG VX-993
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2024-05-09 |
| Est. Completion | 2025-02-18 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06394167
The ClinicalTrials.gov registry entry for NCT06394167 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 88 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vertex Pharmaceuticals Incorporated, which has 191 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT06394167 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06394167 about?
NCT06394167 is a clinical study titled "A Phase 1 Dose Escalation Study of Intravenous VX-993 in Healthy Adults". The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of intravenously administered VX-993 at different doses in healthy participants.
What is the current status of trial NCT06394167?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 88 participants. The study started on 2024-05-09. Estimated completion is 2025-02-18.
What interventions are being tested in trial NCT06394167?
The interventions under investigation include: Placebo (DRUG), VX-993 (DRUG).
Who is sponsoring clinical trial NCT06394167?
This trial is sponsored by Vertex Pharmaceuticals Incorporated, which has 191 total clinical trials registered on ClinicalTrials.gov.
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