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NCT01051700 · ClinicalTrials.gov registry record · Phase 1

A Safety Study in Healthy Volunteers to Evaluate Safety, How Fast the Drug is Absorbed, and the Side Effects of the Drug in Humans

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
72
Enrollment target

NCT01051700 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 72 participants.

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The verdict

NCT01051700, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
72 participants
Enrollment target

Study Summary

This study is to evaluate the safety, absorption rate and side effects associated with the study drug. Healthy volunteers will be given a single dose of the drug in Part 1. Subjects will be dosed at the same time at several different sites. In Part 2 of the study elderly volunteers will participate in a 14 day repeat dose session receiving either study drug or a placebo (sugar pill). Data from at least 7 days of safety will be reviewed from the first set of volunteers before increasing the doses for the next set. All results will be used for planning the next study.

Interventions

  • OTHER Placebo
  • DRUG GW786034

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2010-01-12
Est. Completion 2010-05-27
Phase Phase 1

Sponsor

GlaxoSmithKline

1,345 total trials

What the Registry Record Tells You About NCT01051700

The ClinicalTrials.gov registry entry for NCT01051700 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.

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

NCT01051700 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01051700 about?

NCT01051700 is a clinical study titled "A Safety Study in Healthy Volunteers to Evaluate Safety, How Fast the Drug is Absorbed, and the Side Effects of the Drug in Humans". This study is to evaluate the safety, absorption rate and side effects associated with the study drug. Healthy volunteers will be given a single dose of the drug in Part 1. Subjects will be dosed at the same time at several different sites. In Part 2 of the study elderly volunteers will participate ...

What is the current status of trial NCT01051700?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 72 participants. The study started on 2010-01-12. Estimated completion is 2010-05-27.

What interventions are being tested in trial NCT01051700?

The interventions under investigation include: Placebo (OTHER), GW786034 (DRUG).

Who is sponsoring clinical trial NCT01051700?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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.