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NCT07283770 · ClinicalTrials.gov registry record · Phase 1

Dose Escalation Study Evaluating the Safety and Pharmacokinetics of VX-581 in Healthy Participants

A Phase 1 study of Cystic Fibrosis, sponsored by Vertex Pharmaceuticals Incorporated.

Recruiting
Registry status
Phase 1
Development phase
128
Enrollment target
1
Study location

NCT07283770: Recruiting Phase 1 study of Cystic Fibrosis, sponsored by Vertex Pharmaceuticals Incorporated.

NCT07283770 is a Phase 1 study of Cystic Fibrosis that is actively recruiting participants, run by Vertex Pharmaceuticals Incorporated. The registered enrollment target is 128 participants, below the 178-participant average among 169 other Cystic Fibrosis trials with a reported enrollment target (28% 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

NCT07283770, a Phase 1 study of Cystic Fibrosis, is actively recruiting participants, sponsored by Vertex Pharmaceuticals Incorporated.

RECRUITING
Registry status
Phase 1
Development phase
128 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of single and multiple ascending doses of VX-581.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG VX-581

Study Locations (1)

Kansas

  • Altasciences - Kansas City - Overland Park

Trial Details

FieldValue
Enrollment Target 128 participants
Start Date 2025-12-09
Est. Completion 2026-11-19
Phase Phase 1
Vertex Pharmaceuticals Incorporated

191 total trials

What NCT07283770 shows while recruiting

NCT07283770 is an interventional study that assigns participants to a tested intervention. The registered 128 participants enrollment target is mid-sized for trials with a published cap, below the 178-participant average among 169 other Cystic Fibrosis trials with a reported enrollment target (28% lower).

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

NCT07283770 reports a single indexed study location in Kansas.

Frequently Asked Questions

What is clinical trial NCT07283770 about?

NCT07283770 is a clinical study titled "Dose Escalation Study Evaluating the Safety and Pharmacokinetics of VX-581 in Healthy Participants". The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of single and multiple ascending doses of VX-581.

What is the current status of trial NCT07283770?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 128 participants. The study started on 2025-12-09. Estimated completion is 2026-11-19.

What conditions does trial NCT07283770 study?

This clinical trial studies the following conditions: Cystic Fibrosis.

What interventions are being tested in trial NCT07283770?

The interventions under investigation include: Placebo (DRUG), VX-581 (DRUG).

Who is sponsoring clinical trial NCT07283770?

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

Where is trial NCT07283770 being conducted?

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

Similar trials for Cystic Fibrosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07283770's enrollment target sits among peer trials

128 50th of 169 higher than 120 of 169 other Cystic Fibrosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cystic Fibrosis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07283770, the US trial registry maintained by the National Library of Medicine. NCT07283770 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.