Clinical Trials Directory

Trials / Completed

CompletedNCT00668733

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

Follow-up Study to Evaluate Sustained Clearance Rates of Actinic Keratoses up to One Year After Completion of Studies GW01-0702, GW01-0703, GW01-0704, and GW01-0705

Status
Completed
Phase
Study type
Observational
Enrollment
179 (actual)
Sponsor
Graceway Pharmaceuticals, LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

This is a Phase 3 longitudinal and observational study. Subjects who previously enrolled in studies GW01-0702, GW01-0703, GW01-0704, and GW01-0705 and were completely cleared of their AK lesions in the selected treatment area at the end-of-study visit will return for follow-up visits at 6 and 12 months after the EOS visit or until a recurrence of AKs. The NCT numbers for the above mentioned studies are: NCT00603798 - for Studies GW01-0703 and GW01-0705 NCT00605176 for Studies GW01-0702 and GW01-0704

Conditions

Timeline

Start date
2008-04-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2008-04-29
Last updated
2010-07-20
Results posted
2010-07-13

Source: ClinicalTrials.gov record NCT00668733. Inclusion in this directory is not an endorsement.