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1-Year Follow up to the 1473-IMIQ Study

A Follow-up Study to Evaluate Actinic Keratosis Recurrence Rates One Year After Completion of the 1473-IMIQ Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00114023
Enrollment
84
Registered
2005-06-14
Start date
2005-01-31
Completion date
Unknown
Last updated
2007-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Keratosis

Keywords

AK, Imiquimod 5% cream, 3M Pharmaceuticals, Aldara, Actinic Keratosis

Brief summary

This is a 1-year follow-up study to evaluate the long-term effects in subjects who completely cleared their actinic keratosis (AK) lesions in the 1473-IMIQ study. The 1473-IMIQ study evaluated the safety and effectiveness of imiquimod 5% cream compared to a placebo cream for the treatment of AK.

Interventions

Sponsors

Graceway Pharmaceuticals, LLC
Lead SponsorINDUSTRY

Study design

Observational model
DEFINED_POPULATION
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Subject had to participate in the 1473-IMIQ Study AND have had 100% clearance of AK lesions

Exclusion criteria

* Did not use any topical preparations in the previous treatment area within 24-hours of the scheduled visit.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026