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NCT01072214 · ClinicalTrials.gov registry record · Phase 1

A Safety Study to Evaluate Pazopanib Eye Drops in Healthy Volunteers

A Phase 1 study of Macular Degeneration, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
37
Enrollment target
1
Study location

NCT01072214 is a Phase 1 study of Macular Degeneration that has completed, run by GlaxoSmithKline. The registered enrollment target is 37 participants, below the 178-participant average among 26 other Macular Degeneration trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01072214, a Phase 1 study of Macular Degeneration, has completed, sponsored by GlaxoSmithKline.

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

Study Summary

A study to determine the safety and tolerability of pazopanib eye drops. The study will also determine how the drug is absorbed and metabolized over time. Repeat doses of eye drops will be administered to healthy adult volunteers over a 14-day period with one additional dose given on the 15th day of the session. Three groups of subjects may receive either active drug or placebo (drops without drug). The first group of subjects will receive a maximum of 1.6mg of pazopanib or placebo. The dose of drug to be given to the next two groups will be determined based on the results of the first group of subjects. The last group of subjects will be of Japanese descent.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG pazopanib

Study Locations (1)

California

  • GSK Investigational Site - Glendale

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2010-03-09
Est. Completion 2010-06-28
Phase Phase 1

Sponsor

GlaxoSmithKline

1,345 total trials

What the Registry Record Tells You About NCT01072214

The ClinicalTrials.gov registry entry for NCT01072214 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 178-participant average among 26 other Macular Degeneration trials with a reported enrollment target (79% lower). The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Macular Degeneration appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT01072214 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT01072214 about?

NCT01072214 is a clinical study titled "A Safety Study to Evaluate Pazopanib Eye Drops in Healthy Volunteers". A study to determine the safety and tolerability of pazopanib eye drops. The study will also determine how the drug is absorbed and metabolized over time. Repeat doses of eye drops will be administered to healthy adult volunteers over a 14-day period with one additional dose given on the 15th day of...

What is the current status of trial NCT01072214?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2010-03-09. Estimated completion is 2010-06-28.

What conditions does trial NCT01072214 study?

This clinical trial studies the following conditions: Macular Degeneration.

What interventions are being tested in trial NCT01072214?

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

Who is sponsoring clinical trial NCT01072214?

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

Where is trial NCT01072214 being conducted?

This trial has 1 study location across California. 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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