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NCT02056392 · ClinicalTrials.gov registry record · Phase 1

To Assess the Effects of Single Oral Dose of Selumetinib [AZD6244; ARRY-142886] [Hyd-Sulfate]), on QTc Interval in Healthy Male Volunteers

A Phase 1 study of Solid Tumours, sponsored by AstraZeneca.

Completed
Registry status
Phase 1
Development phase
54
Enrollment target
1
Study location

NCT02056392 is a Phase 1 study of Solid Tumours that has completed, run by AstraZeneca. The registered enrollment target is 54 participants, below the 140-participant average among 9 other Solid Tumours trials with a reported enrollment target (61% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02056392, a Phase 1 study of Solid Tumours, has completed, sponsored by AstraZeneca.

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

Study Summary

Study to assess the effect of Selumetinib \[AZD6244; ARRY-142886\] \[Hyd-Sulfate\]), on QTc interval in healthy male volunteers.

Conditions Studied

Interventions

  • DRUG Moxifloxacin
  • DRUG Selumetinib
  • DRUG selumetinib placebo

Study Locations (1)

Kansas

  • Research Site - Overland Park

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2014-03
Est. Completion 2014-08
Phase Phase 1

Sponsor

AstraZeneca

1,285 total trials

What the Registry Record Tells You About NCT02056392

The ClinicalTrials.gov registry entry for NCT02056392 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 140-participant average among 9 other Solid Tumours trials with a reported enrollment target (61% lower). The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Solid Tumours appearing as the primary indexed condition, and to 3 interventions - of which Moxifloxacin is the first listed.

NCT02056392 reports 1 study location spanning 1 distinct geographic area - top geographies include Kansas.

Frequently Asked Questions

What is clinical trial NCT02056392 about?

NCT02056392 is a clinical study titled "To Assess the Effects of Single Oral Dose of Selumetinib [AZD6244; ARRY-142886] [Hyd-Sulfate]), on QTc Interval in Healthy Male Volunteers". Study to assess the effect of Selumetinib \[AZD6244; ARRY-142886\] \[Hyd-Sulfate\]), on QTc interval in healthy male volunteers.

What is the current status of trial NCT02056392?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2014-03. Estimated completion is 2014-08.

What conditions does trial NCT02056392 study?

This clinical trial studies the following conditions: Solid Tumours.

What interventions are being tested in trial NCT02056392?

The interventions under investigation include: Moxifloxacin (DRUG), Selumetinib (DRUG), selumetinib placebo (DRUG).

Who is sponsoring clinical trial NCT02056392?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02056392 being conducted?

This trial has 1 study location across Kansas. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.