Twelve Week Safety and Efficacy Study With a Topical Gel to Treat Common Warts in Adults
Completed · Phase 2
Conditions studied: Warts
In brief
The primary purpose of this study is to evaluate the effectiveness in adults, of four different strengths of resiquimod gel applied to common wart(s) three times a week for twelve weeks. A second purpose is to evaluate the safety of the drug.
Key facts
- Study ID
- NCT00114920
- Run by
- Graceway Pharmaceuticals, LLC
- People needed
- 88
- Starts
- 2004-03-01
- Last updated by the study team
- 2007-02-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of common warts
- Two forms of birth control
You may not qualify if…
- Pregnant or breast feeding
- Other types of wart(s), ie. plantar
- Currently participating in another clinical study
- Chronic viral hepatitis B or C
Where it is running
- Welborn Clinic — Evansville, Indiana, United States
Full record on ClinicalTrials.gov
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