Trials / Completed
CompletedNCT00114920
Twelve Week Safety and Efficacy Study With a Topical Gel to Treat Common Warts in Adults
A Three-Stage, Modified-Blind, Dose-Escalating Study to Assess Efficacy and Safety of Resiquimod Gel for the Treatment of Common Warts in Adults
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 88 (planned)
- Sponsor
- Graceway Pharmaceuticals, LLC · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Resiquimod |
Timeline
- Start date
- 2004-03-01
- First posted
- 2005-06-21
- Last updated
- 2007-02-19
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00114920. Inclusion in this directory is not an endorsement.