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NCT02062203 · ClinicalTrials.gov registry record · Phase 1

Effect of AKB-6548 on Cardiac Repolarization Intervals in Healthy Volunteers

A Phase 1 study, sponsored by Akebia Therapeutics.

Completed
Registry status
Phase 1
Development phase
50
Enrollment target

NCT02062203: Completed Phase 1 study, sponsored by Akebia Therapeutics.

NCT02062203 is a Phase 1 study that has completed, run by Akebia Therapeutics. The registered enrollment target is 50 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02062203, a Phase 1 study, has completed, sponsored by Akebia Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target

Study Summary

The main purpose of this study is to evaluate the effect of single oral therapeutic and supratherapeutic doses of AKB-6548 on the QT interval.

Interventions

  • DRUG Placebo
  • DRUG Moxifloxacin
  • DRUG AKB-6548 (therapeutic dose)
  • DRUG AKB-6548 (supratherapeutic dose)

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2014-01
Est. Completion 2014-04
Phase Phase 1
Akebia Therapeutics

24 total trials

What the finished NCT02062203 record still lists

NCT02062203 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT02062203 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02062203 about?

NCT02062203 is a clinical study titled "Effect of AKB-6548 on Cardiac Repolarization Intervals in Healthy Volunteers". The main purpose of this study is to evaluate the effect of single oral therapeutic and supratherapeutic doses of AKB-6548 on the QT interval.

What is the current status of trial NCT02062203?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2014-01. Estimated completion is 2014-04.

What interventions are being tested in trial NCT02062203?

The interventions under investigation include: Placebo (DRUG), Moxifloxacin (DRUG), AKB-6548 (therapeutic dose) (DRUG), AKB-6548 (supratherapeutic dose) (DRUG).

Who is sponsoring clinical trial NCT02062203?

This trial is sponsored by Akebia Therapeutics, which has 24 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02062203's enrollment target sits among peer trials

50 973rd of 2000 higher than 984 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 NCT02062203, the US trial registry maintained by the National Library of Medicine. NCT02062203 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.