Follow-up Study to Evaluate Sustained Clearance Rates of Actinic Keratoses up to One Year

NCT00668733 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 179

Last updated 2010-07-20

Study results available
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Summary

The objective of this study was to obtain long-term sustained clearance rates for subjects previously treated with imiquimod creams in studies GW01-0702, GW01-0703, GW01-0704 and GW01-0705.

Conditions

  • Actinic Keratoses

Sponsors & Collaborators

  • Graceway Pharmaceuticals, LLC

    lead INDUSTRY

Principal Investigators

  • Sharon Levy, MD · Graceway Pharmaceuticals, LLC

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2009-07-31
Completion
2009-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00668733 on ClinicalTrials.gov