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NCT07022119 · ClinicalTrials.gov registry record · Phase 1

A Phase 1 Study Evaluating Safety, Tolerability, and Pharmacokinetics of VX-407 in Healthy Participants

A Phase 1 study of Autosomal Dominant Polycystic Kidney Disease (ADPKD), sponsored by Vertex Pharmaceuticals Incorporated.

Active
Registry status
Phase 1
Development phase
32
Enrollment target
1
Study location

NCT07022119: Active Phase 1 study of Autosomal Dominant Polycystic Kidney Disease (ADPKD), sponsored by Vertex Pharmaceuticals Incorporated.

NCT07022119 is a Phase 1 study of Autosomal Dominant Polycystic Kidney Disease (ADPKD) that is active but no longer recruiting, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 32 participants, below the 786-participant average among 5 other Autosomal Dominant Polycystic Kidney Disease (ADPKD) trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07022119, a Phase 1 study of Autosomal Dominant Polycystic Kidney Disease (ADPKD), is active but no longer recruiting, sponsored by Vertex Pharmaceuticals Incorporated.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
32 participants
Enrollment target
1
Study location

Study Summary

The purpose of the study is to evaluate the safety, tolerability and pharmacokinetics of VX-407 in healthy participants.

Interventions

  • DRUG Placebo
  • DRUG VX-407

Study Locations (1)

Kansas

  • ICON Lenexa - Lenexa

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2025-06-12
Est. Completion 2026-03-03
Phase Phase 1
Vertex Pharmaceuticals Incorporated

191 total trials

What the registry record for NCT07022119 still lists

NCT07022119 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 786-participant average among 5 other Autosomal Dominant Polycystic Kidney Disease (ADPKD) trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Autosomal Dominant Polycystic Kidney Disease (ADPKD) appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07022119 reports a single indexed study location in Kansas.

Frequently Asked Questions

What is clinical trial NCT07022119 about?

NCT07022119 is a clinical study titled "A Phase 1 Study Evaluating Safety, Tolerability, and Pharmacokinetics of VX-407 in Healthy Participants". The purpose of the study is to evaluate the safety, tolerability and pharmacokinetics of VX-407 in healthy participants.

What is the current status of trial NCT07022119?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2025-06-12. Estimated completion is 2026-03-03.

What conditions does trial NCT07022119 study?

This clinical trial studies the following conditions: Autosomal Dominant Polycystic Kidney Disease (ADPKD).

What interventions are being tested in trial NCT07022119?

The interventions under investigation include: Placebo (DRUG), VX-407 (DRUG).

Who is sponsoring clinical trial NCT07022119?

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

Where is trial NCT07022119 being conducted?

This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT07022119, the US trial registry maintained by the National Library of Medicine. NCT07022119 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.