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NCT03554304 · ClinicalTrials.gov registry record · Phase 1

Evaluate the Effect of WCK 5222 on the QT/QTc Interval in Healthy Volunteers

A Phase 1 study, sponsored by Wockhardt.

Completed
Registry status
Phase 1
Development phase
60
Enrollment target

NCT03554304: Completed Phase 1 study, sponsored by Wockhardt.

NCT03554304 is a Phase 1 study that has completed, run by Wockhardt. The registered enrollment target is 60 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03554304, a Phase 1 study, has completed, sponsored by Wockhardt.

COMPLETED
Registry status
Phase 1
Development phase
60 participants
Enrollment target

Study Summary

A Randomized, Double-Blind, Double-Dummy, Placebo- and Positive-Controlled, Crossover Study to Evaluate the Effect of WCK 5222 on the QT/QTc Interval in Healthy Volunteers

Primary Outcome

as shown by analysis of the QT interval.

Interventions

  • DRUG WCK 5222
  • DRUG IV placebo matched to WCK 5222 / Moxifloxacin IV solution
  • DRUG Moxifloxacin 400-mg

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2017-02-09
Est. Completion 2017-10-06
Phase Phase 1
Wockhardt

27 total trials

What the finished NCT03554304 record still lists

NCT03554304 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

The record links to 0 conditions, and to 3 interventions - of which WCK 5222 is the first listed.

NCT03554304 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03554304 about?

NCT03554304 is a clinical study titled "Evaluate the Effect of WCK 5222 on the QT/QTc Interval in Healthy Volunteers". A Randomized, Double-Blind, Double-Dummy, Placebo- and Positive-Controlled, Crossover Study to Evaluate the Effect of WCK 5222 on the QT/QTc Interval in Healthy Volunteers

What is the current status of trial NCT03554304?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2017-02-09. Estimated completion is 2017-10-06.

What interventions are being tested in trial NCT03554304?

The interventions under investigation include: WCK 5222 (DRUG), IV placebo matched to WCK 5222 / Moxifloxacin IV solution (DRUG), Moxifloxacin 400-mg (DRUG).

Who is sponsoring clinical trial NCT03554304?

This trial is sponsored by Wockhardt, which has 27 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03554304's enrollment target sits among peer trials

60 831st of 2000 higher than 1,106 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 NCT03554304, the US trial registry maintained by the National Library of Medicine. NCT03554304 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.