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NCT06258265 · ClinicalTrials.gov registry record · Phase 1

A Study of TAK-279 in Healthy Adults on the Effect on ECG Measurements

A Phase 1 study of Healthy Volunteers, sponsored by Takeda.

Completed
Registry status
Phase 1
Development phase
120
Enrollment target
1
Study location

NCT06258265 is a Phase 1 study of Healthy Volunteers that has completed, run by Takeda. The registered enrollment target is 120 participants, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06258265, a Phase 1 study of Healthy Volunteers, has completed, sponsored by Takeda.

COMPLETED
Registry status
Phase 1
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

The main aim of this study is to find out how more than one dose of TAK-279 changes the heart-rate corrected QT (QTc) interval of healthy adults. A QTc interval is a measurement on an electrocardiogram (ECG) and shows the time when the heart contracts until it finishes relaxing. Other aims are to learn about the effect of several doses of TAK-279 on other ECG measurements of healthy adults, how the body of a healthy adult processes TAK-279 and moxifloxacin (pharmacokinetics), and to learn about the side effects of TAK-279 and how well it is tolerated when given to healthy adults. The participants will be given TAK-279 and moxifloxacin or a placebo for 7 days. During the study, participants will need to stay at the clinic for 10 days.

Conditions Studied

Interventions

  • DRUG TAK-279
  • DRUG Moxifloxacin
  • DRUG Moxifloxacin Placebo
  • DRUG TAK-279 Placebo

Study Locations (1)

Arizona

  • Celerion - Tempe

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2024-04-29
Est. Completion 2024-07-09
Phase Phase 1

Sponsor

Takeda

408 total trials

What the Registry Record Tells You About NCT06258265

The ClinicalTrials.gov registry entry for NCT06258265 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (75% lower). The listed sponsor is Takeda, which has 408 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Volunteers appearing as the primary indexed condition, and to 4 interventions - of which TAK-279 is the first listed.

NCT06258265 reports 1 study location spanning 1 distinct geographic area - top geographies include Arizona.

Frequently Asked Questions

What is clinical trial NCT06258265 about?

NCT06258265 is a clinical study titled "A Study of TAK-279 in Healthy Adults on the Effect on ECG Measurements". The main aim of this study is to find out how more than one dose of TAK-279 changes the heart-rate corrected QT (QTc) interval of healthy adults. A QTc interval is a measurement on an electrocardiogram (ECG) and shows the time when the heart contracts until it finishes relaxing. Other aims are to le...

What is the current status of trial NCT06258265?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 120 participants. The study started on 2024-04-29. Estimated completion is 2024-07-09.

What conditions does trial NCT06258265 study?

This clinical trial studies the following conditions: Healthy Volunteers.

What interventions are being tested in trial NCT06258265?

The interventions under investigation include: TAK-279 (DRUG), Moxifloxacin (DRUG), Moxifloxacin Placebo (DRUG), TAK-279 Placebo (DRUG).

Who is sponsoring clinical trial NCT06258265?

This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06258265 being conducted?

This trial has 1 study location across Arizona. 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

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