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NCT05727800 · ClinicalTrials.gov registry record · Phase 1

A Phase 1, First-in-human Study of VX-668

A Phase 1 study of Alpha-1 Antitrypsin Deficiency, sponsored by Vertex Pharmaceuticals Incorporated.

Completed
Registry status
Phase 1
Development phase
114
Enrollment target
5
Study locations

NCT05727800 is a Phase 1 study of Alpha-1 Antitrypsin Deficiency that has completed, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 114 participants, below the 3,072-participant average among 18 other Alpha-1 Antitrypsin Deficiency trials with a reported enrollment target (96% lower). The trial reports 5 study locations across 4 states.

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The verdict

NCT05727800, a Phase 1 study of Alpha-1 Antitrypsin Deficiency, has completed, sponsored by Vertex Pharmaceuticals Incorporated.

COMPLETED
Registry status
Phase 1
Development phase
114 participants
Enrollment target
5
Study locations

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of VX-668 at various doses.

Interventions

  • DRUG Placebo
  • DRUG VX-668

Study Locations (5)

Florida

  • University of Florida - Gainesville
  • Central Florida Pulmonary Group, P.A. - Orlando

Arizona

  • Celerion - Tempe - Tempe

Kansas

  • ICON Lenexa - Lenexa

Utah

  • ICON Salt Lake City - Salt Lake City

Trial Details

FieldValue
Enrollment Target 114 participants
Start Date 2023-02-08
Est. Completion 2024-02-13
Phase Phase 1

Sponsor

Vertex Pharmaceuticals Incorporated

191 total trials

What the Registry Record Tells You About NCT05727800

The ClinicalTrials.gov registry entry for NCT05727800 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 114 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,072-participant average among 18 other Alpha-1 Antitrypsin Deficiency trials with a reported enrollment target (96% lower). The listed sponsor is Vertex Pharmaceuticals Incorporated, which has 191 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Alpha-1 Antitrypsin Deficiency appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT05727800 reports 5 study locations spanning 4 distinct geographic areas - top geographies include Florida, Arizona, Kansas.

Frequently Asked Questions

What is clinical trial NCT05727800 about?

NCT05727800 is a clinical study titled "A Phase 1, First-in-human Study of VX-668". The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of VX-668 at various doses.

What is the current status of trial NCT05727800?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 114 participants. The study started on 2023-02-08. Estimated completion is 2024-02-13.

What conditions does trial NCT05727800 study?

This clinical trial studies the following conditions: Alpha-1 Antitrypsin Deficiency.

What interventions are being tested in trial NCT05727800?

The interventions under investigation include: Placebo (DRUG), VX-668 (DRUG).

Who is sponsoring clinical trial NCT05727800?

This trial is sponsored by Vertex Pharmaceuticals Incorporated, which has 191 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05727800 being conducted?

This trial has 5 study locations across Arizona, Florida, Kansas, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.