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NCT06422767 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Effect of Bepirovirsen on Cardiac Conduction as Assessed by 12-lead Electrocardiogram in Healthy Volunteers

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
46
Enrollment target

NCT06422767: Completed Phase 1 study, sponsored by GlaxoSmithKline.

NCT06422767 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 46 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06422767, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
46 participants
Enrollment target

Study Summary

This study will evaluate the effect of a single dose of bepirovirsen on the QT interval corrected by Fridericia's formula (QTcF) as compared to placebo. The data generated will be used to model the relationship between bepirovirsen concentration and QTcF.

Primary Outcome

Continuous 12-lead electrocardiogram (ECG) was captured by Holter monitor. QTcF was measured from 10 digital ECGs extracted from the continuous tracing after 10 minutes of rest in supine position. Baseline was defined as pre-dose value on Day 1. Change from Baseline (CFB) was calculated by subtracting post-dose visit value from Baseline value. Geometric mean and 90 percent (%) Confidence Interval (CI) of predicted CFB QTcF adjusted for placebo at Cmax following supratherapeutic single doses of B

Interventions

  • DRUG Placebo
  • DRUG Bepirovirsen

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2024-07-18
Est. Completion 2025-04-28
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT06422767 record still lists

NCT06422767 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT06422767 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06422767 about?

NCT06422767 is a clinical study titled "Study to Evaluate the Effect of Bepirovirsen on Cardiac Conduction as Assessed by 12-lead Electrocardiogram in Healthy Volunteers". This study will evaluate the effect of a single dose of bepirovirsen on the QT interval corrected by Fridericia's formula (QTcF) as compared to placebo. The data generated will be used to model the relationship between bepirovirsen concentration and QTcF.

What is the current status of trial NCT06422767?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 46 participants. The study started on 2024-07-18. Estimated completion is 2025-04-28.

What interventions are being tested in trial NCT06422767?

The interventions under investigation include: Placebo (DRUG), Bepirovirsen (DRUG).

Who is sponsoring clinical trial NCT06422767?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06422767's enrollment target sits among peer trials

46 1058th of 2000 higher than 935 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT06422767, the US trial registry maintained by the National Library of Medicine. NCT06422767 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.