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.