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NCT00115154 · ClinicalTrials.gov registry record · Phase 4

Study to Assess the Safety and Efficacy of Imiquimod 5% Cream for the Treatment of Actinic Keratosis on the Arms and Hands

A Phase 4 study of Keratosis, sponsored by Graceway Pharmaceuticals.

Completed
Registry status
Phase 4
Development phase
270
Enrollment target
18
Study locations

NCT00115154 is a Phase 4 study of Keratosis that has completed, run by Graceway Pharmaceuticals. The registered enrollment target is 270 participants. The trial reports 18 study locations across 15 states.

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The verdict

NCT00115154, a Phase 4 study of Keratosis, has completed, sponsored by Graceway Pharmaceuticals.

COMPLETED
Registry status
Phase 4
Development phase
270 participants
Enrollment target
18
Study locations

Study Summary

The purpose of this study is to evaluate the safety and efficacy of imiquimod 5% cream compared to vehicle cream in the treatment of Actinic Keratosis (AK) on the arm and/or hand when the cream is applied once daily 2 days per week for 16 weeks.

Conditions Studied

Interventions

  • DRUG Aldara (imiquimod) cream, 5%

Study Locations (18)

Georgia

  • - Atlanta
  • - Newnan

New York

  • - New York
  • - Rochester

Texas

  • - Dallas
  • - Houston

Arizona

  • - Tucson

California

  • - Vista

Illinois

  • - Buffalo Grove

Indiana

  • - Evansville

New Jersey

  • - Riverside Park

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2005-05
Est. Completion 2006-09
Phase Phase 4

Sponsor

Graceway Pharmaceuticals

17 total trials

What the Registry Record Tells You About NCT00115154

The ClinicalTrials.gov registry entry for NCT00115154 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 270 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Graceway Pharmaceuticals, which has 17 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Keratosis appearing as the primary indexed condition, and to 1 intervention - of which Aldara (imiquimod) cream, 5% is the first listed.

NCT00115154 reports 18 study locations spanning 15 distinct geographic areas - top geographies include Georgia, New York, Texas.

Frequently Asked Questions

What is clinical trial NCT00115154 about?

NCT00115154 is a clinical study titled "Study to Assess the Safety and Efficacy of Imiquimod 5% Cream for the Treatment of Actinic Keratosis on the Arms and Hands". The purpose of this study is to evaluate the safety and efficacy of imiquimod 5% cream compared to vehicle cream in the treatment of Actinic Keratosis (AK) on the arm and/or hand when the cream is applied once daily 2 days per week for 16 weeks.

What is the current status of trial NCT00115154?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 270 participants. The study started on 2005-05. Estimated completion is 2006-09.

What conditions does trial NCT00115154 study?

This clinical trial studies the following conditions: Keratosis.

What interventions are being tested in trial NCT00115154?

The interventions under investigation include: Aldara (imiquimod) cream, 5% (DRUG).

Who is sponsoring clinical trial NCT00115154?

This trial is sponsored by Graceway Pharmaceuticals, which has 17 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00115154 being conducted?

This trial has 18 study locations across Arizona, California, Georgia, Illinois, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Keratosis

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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.